US20150274762A1 - Metal complexes, methods, and uses thereof - Google Patents
Metal complexes, methods, and uses thereof Download PDFInfo
- Publication number
- US20150274762A1 US20150274762A1 US14/437,963 US201314437963A US2015274762A1 US 20150274762 A1 US20150274762 A1 US 20150274762A1 US 201314437963 A US201314437963 A US 201314437963A US 2015274762 A1 US2015274762 A1 US 2015274762A1
- Authority
- US
- United States
- Prior art keywords
- independently
- cycloalkane
- substituted
- amino
- aryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 0 *C([2H])(C)N.*C([2H])(C)N.C.C.C.C Chemical compound *C([2H])(C)N.*C([2H])(C)N.C.C.C.C 0.000 description 143
- RIRARCHMRDHZAR-UHFFFAOYSA-N CC1CCCC1C Chemical compound CC1CCCC1C RIRARCHMRDHZAR-UHFFFAOYSA-N 0.000 description 5
- AEHISSLCRMGFIZ-UHFFFAOYSA-N CC1=C(C)C2=C(C=C1)C1=C(C=CC=C1)C2C Chemical compound CC1=C(C)C2=C(C=C1)C1=C(C=CC=C1)C2C AEHISSLCRMGFIZ-UHFFFAOYSA-N 0.000 description 4
- KPUYNEAPWNTHHZ-UHFFFAOYSA-N CC1=N(C)C2=C(C=CC=C2)[U]1.CC1=N(C)C=C2C3=CC=CC=C3C3=CC=CC=C3N21.CC1=[N+](C)C2=C(C=CC=C2)N1C.CN1C2=C(C=CC=C2)C=N1C Chemical compound CC1=N(C)C2=C(C=CC=C2)[U]1.CC1=N(C)C=C2C3=CC=CC=C3C3=CC=CC=C3N21.CC1=[N+](C)C2=C(C=CC=C2)N1C.CN1C2=C(C=CC=C2)C=N1C KPUYNEAPWNTHHZ-UHFFFAOYSA-N 0.000 description 4
- WXKQEMTUMAFAHI-PJYRRTDGSA-N CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=C[U]C=N1C.CC1=N(C)C=C[U]1.CC1=[N+](C)C=CN1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CN/C(C)=C\C=C/[U].CN1C=C2C=CC=CC2=N1C.CN1C=CC=N1C Chemical compound CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=C[U]C=N1C.CC1=N(C)C=C[U]1.CC1=[N+](C)C=CN1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CN/C(C)=C\C=C/[U].CN1C=C2C=CC=CC2=N1C.CN1C=CC=N1C WXKQEMTUMAFAHI-PJYRRTDGSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N Cc1ccccc1C Chemical compound Cc1ccccc1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- QBYJAKIGLGVSBD-UHFFFAOYSA-O C/C1=[SH]/[Mn]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Mn]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Mn]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Mn]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Mn]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C Chemical compound C/C1=[SH]/[Mn]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Mn]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Mn]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Mn]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Mn]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C QBYJAKIGLGVSBD-UHFFFAOYSA-O 0.000 description 2
- VECYDXQNXUEMLA-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1CCCC61)N1=C4C(=CC=C1)C1=C(C=CC=C1)N34)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)N1C4=C(C=CC=C4)C4=CC=CN(=C41)C31C3=C4C(=CC=C3C3CCCC31)C1=C(C=CC=C1)N42.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)N3C5=C(C=CC=C5)C5=CC=CN(=C53)C43C4=C1C2=CC=C4C1CCCC13.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1CCCC61)N1=C(C=C4C(=C1)[U]C1=C4C=CC=C1)N23.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1CCCC61)N1=C(C=C4[U]C5=C(C=CC=C5)C4=C1)N23 Chemical compound C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1CCCC61)N1=C4C(=CC=C1)C1=C(C=CC=C1)N34)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)N1C4=C(C=CC=C4)C4=CC=CN(=C41)C31C3=C4C(=CC=C3C3CCCC31)C1=C(C=CC=C1)N42.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)N3C5=C(C=CC=C5)C5=CC=CN(=C53)C43C4=C1C2=CC=C4C1CCCC13.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1CCCC61)N1=C(C=C4C(=C1)[U]C1=C4C=CC=C1)N23.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1CCCC61)N1=C(C=C4[U]C5=C(C=CC=C5)C4=C1)N23 VECYDXQNXUEMLA-UHFFFAOYSA-N 0.000 description 2
- VKRFKRUVIOLXBW-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=C/C=C5C(=C/21)/C4(C1CCCC31)N1=C2C(=CC=C1)C1=C(C=CC=C1)N2/5.C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=CC=C5C(=C21)C4(C1CCCC51)N1=C2C(=CC=C1)C1=C(C=CC=C1)N32.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)N1C2=C(C=CC=C2)C2=CC=CN(=C21)C41C2=C4C(=CC=C2C2CCCC21)C1=C(C=CC=C1)N34.C1=CC2=C(C=C1)N1C3=N(C=CC=C23)C23C4=C(C=CC=C4C4CCCC42)N2C4=C(C=CC=C4)C4=C/C=C1/C3=C\42 Chemical compound C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=C/C=C5C(=C/21)/C4(C1CCCC31)N1=C2C(=CC=C1)C1=C(C=CC=C1)N2/5.C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=CC=C5C(=C21)C4(C1CCCC51)N1=C2C(=CC=C1)C1=C(C=CC=C1)N32.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)N1C2=C(C=CC=C2)C2=CC=CN(=C21)C41C2=C4C(=CC=C2C2CCCC21)C1=C(C=CC=C1)N34.C1=CC2=C(C=C1)N1C3=N(C=CC=C23)C23C4=C(C=CC=C4C4CCCC42)N2C4=C(C=CC=C4)C4=C/C=C1/C3=C\42 VKRFKRUVIOLXBW-UHFFFAOYSA-N 0.000 description 2
- NVAWWEICBYPFSM-UHFFFAOYSA-P C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Mn]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Mn]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Mn]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Mn]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Mn]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Mn]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Mn]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Mn]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 NVAWWEICBYPFSM-UHFFFAOYSA-P 0.000 description 2
- IOIQCIVSTGNMFC-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Mn]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Mn]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Mn]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Mn]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Mn]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Mn]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Mn]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Mn]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 IOIQCIVSTGNMFC-UHFFFAOYSA-N 0.000 description 2
- GKIBNUFOOBKASX-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Mn]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Mn]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Mn]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Mn]342 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Mn]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Mn]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Mn]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Mn]342 GKIBNUFOOBKASX-UHFFFAOYSA-O 0.000 description 2
- GWQSGGHRRNCRCB-UHFFFAOYSA-O C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Mn]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Mn]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Mn]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Mn]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Mn]43N3/C=N(/C)C1=C23 Chemical compound C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Mn]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Mn]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Mn]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Mn]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Mn]43N3/C=N(/C)C1=C23 GWQSGGHRRNCRCB-UHFFFAOYSA-O 0.000 description 2
- WVVXSGDFHXPGPJ-UHFFFAOYSA-N C1=CN=C(C2=CC=C3C(=C2)N(C2=C/C4=C(\C=C/2)C2=C(C=CC=C2)N4C2=NC=CC=C2)C2=C3C=CC=C2)C=C1 Chemical compound C1=CN=C(C2=CC=C3C(=C2)N(C2=C/C4=C(\C=C/2)C2=C(C=CC=C2)N4C2=NC=CC=C2)C2=C3C=CC=C2)C=C1 WVVXSGDFHXPGPJ-UHFFFAOYSA-N 0.000 description 2
- DVIZYIPYUBSTQS-UHFFFAOYSA-O CC1=[SH][Mn]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Mn]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Mn]\321.CN1CCN2C3=C1N1C4=C3[Mn]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Mn]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Mn]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Mn]\321.CN1CCN2C3=C1N1C4=C3[Mn]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 DVIZYIPYUBSTQS-UHFFFAOYSA-O 0.000 description 2
- FXSCJZNMWILAJO-UHFFFAOYSA-N BrC1=C/C2=C(\C=C/1)C1=C(C=CC=C1)C2 Chemical compound BrC1=C/C2=C(\C=C/1)C1=C(C=CC=C1)C2 FXSCJZNMWILAJO-UHFFFAOYSA-N 0.000 description 1
- RDNBQLKCMFLYLS-UHFFFAOYSA-N BrC1=C/C2=C(\C=C/1)C1=C(C=CC=C1)N2C1=CC=CC=N1 Chemical compound BrC1=C/C2=C(\C=C/1)C1=C(C=CC=C1)N2C1=CC=CC=N1 RDNBQLKCMFLYLS-UHFFFAOYSA-N 0.000 description 1
- BVBMCLYEEOBHNI-UHFFFAOYSA-N C.CC1=CC=CC2=C1C(C)C1=C(C=CC=C1)C2.CC1=CC=CC2=C1C(C)C1CCCCC1C2.CCC1=C(C)C=CC=C1C Chemical compound C.CC1=CC=CC2=C1C(C)C1=C(C=CC=C1)C2.CC1=CC=CC2=C1C(C)C1CCCCC1C2.CCC1=C(C)C=CC=C1C BVBMCLYEEOBHNI-UHFFFAOYSA-N 0.000 description 1
- UCYVLOAZGFLLQV-UHFFFAOYSA-N C/C1=C/[Ag]23C4=C(C=CC5=C4P1C1=C(C=CC=C1)O5)N1C4=C(C=CC=C4)SC4=C1/C2=C(/C=C/4)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C(C=CC=C4)C4=COC5=C4C2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1/C=C2\C3=C1N(C)=CC3[Ag]13C4=C2/C=C/C2=C\4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C/C1=C/[Ag]23C4=C(C=CC5=C4P1C1=C(C=CC=C1)O5)N1C4=C(C=CC=C4)SC4=C1/C2=C(/C=C/4)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C(C=CC=C4)C4=COC5=C4C2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1/C=C2\C3=C1N(C)=CC3[Ag]13C4=C2/C=C/C2=C\4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 UCYVLOAZGFLLQV-UHFFFAOYSA-N 0.000 description 1
- QWXNVWRDLCMAPL-UHFFFAOYSA-N C/C1=C/[Au]23C4=C(C=CC5=C4P1C1=C(C=CC=C1)O5)N1C4=C(C=CC=C4)SC4=C1/C2=C(/C=C/4)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4)C4=COC5=C4C2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1/C=C2\C3=C1N(C)=CC3[Au]13C4=C2/C=C/C2=C\4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C/C1=C/[Au]23C4=C(C=CC5=C4P1C1=C(C=CC=C1)O5)N1C4=C(C=CC=C4)SC4=C1/C2=C(/C=C/4)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4)C4=COC5=C4C2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1/C=C2\C3=C1N(C)=CC3[Au]13C4=C2/C=C/C2=C\4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 QWXNVWRDLCMAPL-UHFFFAOYSA-N 0.000 description 1
- DMJGKTSIMIXHQT-UHFFFAOYSA-N C/C1=C/[Co]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Co]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Co]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C/C1=C/[Co]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Co]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Co]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 DMJGKTSIMIXHQT-UHFFFAOYSA-N 0.000 description 1
- RNYXPNQXRADDMG-UHFFFAOYSA-N C/C1=C/[Cu]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Cu]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Cu]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C/C1=C/[Cu]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Cu]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Cu]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 RNYXPNQXRADDMG-UHFFFAOYSA-N 0.000 description 1
- OSPWRODLQVZCDR-UHFFFAOYSA-N C/C1=C/[Cu]23C4=C(C=CC5=C4P1C1=C(C=CC=C1)O5)N1C4=C(C=CC=C4)SC4=C1/C2=C(/C=C/4)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C(C=CC=C4)C4=COC5=C4C2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1/C=C2\C3=C1N(C)=CC3[Cu]13C4=C2/C=C/C2=C\4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C/C1=C/[Cu]23C4=C(C=CC5=C4P1C1=C(C=CC=C1)O5)N1C4=C(C=CC=C4)SC4=C1/C2=C(/C=C/4)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C(C=CC=C4)C4=COC5=C4C2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1/C=C2\C3=C1N(C)=CC3[Cu]13C4=C2/C=C/C2=C\4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 OSPWRODLQVZCDR-UHFFFAOYSA-N 0.000 description 1
- GGKQPQNQGXJXRN-UHFFFAOYSA-N C/C1=C/[Ir]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Ir]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Ir]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C/C1=C/[Ir]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Ir]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Ir]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 GGKQPQNQGXJXRN-UHFFFAOYSA-N 0.000 description 1
- YCIXOACHZFNGRD-UHFFFAOYSA-N C/C1=C/[Mn]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Mn]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Mn]243.CN1C=C2C3=C1N(C)=CC3[Mn]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C/C1=C/[Mn]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Mn]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Mn]243.CN1C=C2C3=C1N(C)=CC3[Mn]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 YCIXOACHZFNGRD-UHFFFAOYSA-N 0.000 description 1
- NXNSEUVWWRSUGO-UHFFFAOYSA-N C/C1=C/[Ni]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Ni]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ni]243.CN1C=C2C3=C1N(C)=CC3N13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C/C1=C/[Ni]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Ni]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ni]243.CN1C=C2C3=C1N(C)=CC3N13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 NXNSEUVWWRSUGO-UHFFFAOYSA-N 0.000 description 1
- OQZVSRILBVJRGN-UHFFFAOYSA-N C/C1=C/[Pd]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Pd]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Pd]243.CN1C=C2C3=C1N(C)=CC3[Pd]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C/C1=C/[Pd]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Pd]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Pd]243.CN1C=C2C3=C1N(C)=CC3[Pd]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 OQZVSRILBVJRGN-UHFFFAOYSA-N 0.000 description 1
- KPXALZLQJPPIFR-UHFFFAOYSA-N C/C1=C/[Pt]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Pt]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Pt]243.CN1C=C2C3=C1N(C)=CC3[Pt]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C/C1=C/[Pt]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Pt]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Pt]243.CN1C=C2C3=C1N(C)=CC3[Pt]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 KPXALZLQJPPIFR-UHFFFAOYSA-N 0.000 description 1
- CIQKVVNXVGXOPF-UHFFFAOYSA-N C/C1=C/[Rh]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Rh]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Rh]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C/C1=C/[Rh]2(N3=CC=CC4=C3N(C=C4)C3=N2C2=C(C=C3)SC3=C(C=CC=C3)N2)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C(=C2)[Rh]23N4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C(C5=C(C=CC=C5)O4)/C4=C/C=C\C5=C4N1=C(O5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4.CN1C=C2C3=C1N(C)=CN3[Rh]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=C2)SC2=C(C=CC=C2)C1[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 CIQKVVNXVGXOPF-UHFFFAOYSA-N 0.000 description 1
- FRJCNMUOCVRGKZ-UHFFFAOYSA-N C/C1=C/[Zn]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Zn]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Zn]243.CN1C=C2C3=C1N(C)=CC3[Zn]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C/C1=C/[Zn]23N4=CC=CC5=C4N(C=C5)C4=N\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=N3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Zn]23C4=C/C=C/C=C\4C4=N2C2=C(C=C4)C4=C(C=CC=C4)N2C2=N3C3=C(C=C2)C2=C(C=CC=C2)C13.CC1=CC(C)=C2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Zn]243.CN1C=C2C3=C1N(C)=CC3[Zn]13N4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 FRJCNMUOCVRGKZ-UHFFFAOYSA-N 0.000 description 1
- BHIXNYVIFKGYGE-UHFFFAOYSA-N C/C1=N/[Ag]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1N1=C(C=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Ag]231.CN1CCN2C3=C(C=CC=C3)[Ag]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C/C1=N/[Ag]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1N1=C(C=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Ag]231.CN1CCN2C3=C(C=CC=C3)[Ag]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N3CCN(C)N5C1=C2N4=C35 BHIXNYVIFKGYGE-UHFFFAOYSA-N 0.000 description 1
- JGDXOULXHMTKMB-UHFFFAOYSA-N C/C1=N/[Cu]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1N1=C(C=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Cu]231.CN1CCN2C3=C(C=CC=C3)[Cu]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C/C1=N/[Cu]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1N1=C(C=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Cu]231.CN1CCN2C3=C(C=CC=C3)[Cu]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N3CCN(C)N5C1=C2N4=C35 JGDXOULXHMTKMB-UHFFFAOYSA-N 0.000 description 1
- UEWUIVRCXDMAQL-UHFFFAOYSA-N C/C1=N/[Mn]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Mn]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Mn]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C/C1=N/[Mn]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Mn]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Mn]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 UEWUIVRCXDMAQL-UHFFFAOYSA-N 0.000 description 1
- DNZYIJZHYIIUQZ-UHFFFAOYSA-N C/C1=N/[Ni]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Ni]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Ni]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C/C1=N/[Ni]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Ni]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Ni]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 DNZYIJZHYIIUQZ-UHFFFAOYSA-N 0.000 description 1
- YBOFEVFMWFOPML-UHFFFAOYSA-N C/C1=N/[Pd]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Pd]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Pd]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C/C1=N/[Pd]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Pd]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Pd]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 YBOFEVFMWFOPML-UHFFFAOYSA-N 0.000 description 1
- GBAWOQLTVHKUSS-UHFFFAOYSA-N C/C1=N/[Pt]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Pt]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Pt]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C/C1=N/[Pt]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Pt]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Pt]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 GBAWOQLTVHKUSS-UHFFFAOYSA-N 0.000 description 1
- MDIFQTFQRVOYDR-UHFFFAOYSA-N C/C1=N/[Zn]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Zn]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Zn]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C/C1=N/[Zn]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=C(C=CC=C4)C4=CSC5=C4N2=C2N(C4=CC=CC1=N43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Zn]3(C5=CC=CC=C54)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1CCN2C3=C(C=CC=C3)[Zn]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N3CCN(C)N5C1=C2N4=C35 MDIFQTFQRVOYDR-UHFFFAOYSA-N 0.000 description 1
- YCLVBMSYKGNUDP-UHFFFAOYSA-O C/C1=P/[Ag]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Ag]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Ag]4(C3/C=N(/C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Ag]21[PH](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=P/[Ag]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Ag]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Ag]4(C3/C=N(/C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Ag]21[PH](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 YCLVBMSYKGNUDP-UHFFFAOYSA-O 0.000 description 1
- OWNQXOIXNOGHRC-UHFFFAOYSA-O C/C1=P/[Au]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Au]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Au]4(C3/C=N(/C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Au]21[PH](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=P/[Au]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Au]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Au]4(C3/C=N(/C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Au]21[PH](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 OWNQXOIXNOGHRC-UHFFFAOYSA-O 0.000 description 1
- SCRLOKSUIQRAIC-UHFFFAOYSA-O C/C1=P/[Cu]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Cu]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Cu]4(C3/C=N(/C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Cu]21[PH](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=P/[Cu]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Cu]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Cu]4(C3/C=N(/C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Cu]21[PH](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 SCRLOKSUIQRAIC-UHFFFAOYSA-O 0.000 description 1
- QOWINFSSEQRVJA-UHFFFAOYSA-P C/C1=[PH](\C)[Co]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Co]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Co]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Co]231.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 Chemical compound C/C1=[PH](\C)[Co]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Co]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Co]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Co]231.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 QOWINFSSEQRVJA-UHFFFAOYSA-P 0.000 description 1
- PMDFTHLQDYXURZ-UHFFFAOYSA-P C/C1=[PH](\C)[Cu]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Cu]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Cu]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Cu]231.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 Chemical compound C/C1=[PH](\C)[Cu]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Cu]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Cu]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Cu]231.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 PMDFTHLQDYXURZ-UHFFFAOYSA-P 0.000 description 1
- ROHWKAUKIDDFGW-UHFFFAOYSA-P C/C1=[PH](\C)[Ir]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Ir]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Ir]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Ir]231.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 Chemical compound C/C1=[PH](\C)[Ir]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Ir]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Ir]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Ir]231.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 ROHWKAUKIDDFGW-UHFFFAOYSA-P 0.000 description 1
- PRPPCNQQANVLNF-UHFFFAOYSA-P C/C1=[PH](\C)[Rh]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Rh]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Rh]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Rh]231.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 Chemical compound C/C1=[PH](\C)[Rh]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Rh]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N/3[Rh]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Rh]231.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13 PRPPCNQQANVLNF-UHFFFAOYSA-P 0.000 description 1
- WHRXLUOFSHUCCX-UHFFFAOYSA-O C/C1=[SH]/[Ag]23C4=CC=CC5=C4N(C=C5)C4=C\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=C3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Ag]23C4=C(C=CC5=C4N(C4=C5C=CC=C4)C4=C2C2=C(C=C4)C4=C(C=CC=C4)C21)C1=C/C=C/C=C\13.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ag]432.CN1C=C2C3=C1N(C)=CC3[Ag]13C4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C/C1=[SH]/[Ag]23C4=CC=CC5=C4N(C=C5)C4=C\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=C3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Ag]23C4=C(C=CC5=C4N(C4=C5C=CC=C4)C4=C2C2=C(C=C4)C4=C(C=CC=C4)C21)C1=C/C=C/C=C\13.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ag]432.CN1C=C2C3=C1N(C)=CC3[Ag]13C4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 WHRXLUOFSHUCCX-UHFFFAOYSA-O 0.000 description 1
- ZWAKAQGUNWYRBD-UHFFFAOYSA-N C/C1=[SH]/[Ag]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=C52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C(=CS5)C5=N2C=CC=C5)C3=C14.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1CCN2C3=C1N1C4=C3[Ag]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N4CCN1C)N1=C2C=CC=C1 Chemical compound C/C1=[SH]/[Ag]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=C52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C(=CS5)C5=N2C=CC=C5)C3=C14.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1CCN2C3=C1N1C4=C3[Ag]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N4CCN1C)N1=C2C=CC=C1 ZWAKAQGUNWYRBD-UHFFFAOYSA-N 0.000 description 1
- HQNFUGMMJKSLFU-UHFFFAOYSA-O C/C1=[SH]/[Au]23C4=CC=CC5=C4N(C=C5)C4=C\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=C3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Au]23C4=C(C=CC5=C4N(C4=C5C=CC=C4)C4=C2C2=C(C=C4)C4=C(C=CC=C4)C21)C1=C/C=C/C=C\13.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Au]432.CN1C=C2C3=C1N(C)=CC3[Au]13C4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C/C1=[SH]/[Au]23C4=CC=CC5=C4N(C=C5)C4=C\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=C3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Au]23C4=C(C=CC5=C4N(C4=C5C=CC=C4)C4=C2C2=C(C=C4)C4=C(C=CC=C4)C21)C1=C/C=C/C=C\13.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Au]432.CN1C=C2C3=C1N(C)=CC3[Au]13C4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 HQNFUGMMJKSLFU-UHFFFAOYSA-O 0.000 description 1
- UOFDAFPCNSUHQR-UHFFFAOYSA-N C/C1=[SH]/[Au]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=C52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C(=CS5)C5=N2C=CC=C5)C3=C14.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1CCN2C3=C1N1C4=C3[Au]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N4CCN1C)N1=C2C=CC=C1 Chemical compound C/C1=[SH]/[Au]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=C52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C(=CS5)C5=N2C=CC=C5)C3=C14.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1CCN2C3=C1N1C4=C3[Au]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N4CCN1C)N1=C2C=CC=C1 UOFDAFPCNSUHQR-UHFFFAOYSA-N 0.000 description 1
- CNBNIJJCUCSTDP-UHFFFAOYSA-O C/C1=[SH]/[Co]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Co]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Co]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C/C1=[SH]/[Co]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Co]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Co]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 CNBNIJJCUCSTDP-UHFFFAOYSA-O 0.000 description 1
- JBOSAMFHFUENQV-UHFFFAOYSA-O C/C1=[SH]/[Co]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Co]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Co]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Co]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Co]4(N4C=N(C)C1=C24)N7=C35 Chemical compound C/C1=[SH]/[Co]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Co]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Co]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Co]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Co]4(N4C=N(C)C1=C24)N7=C35 JBOSAMFHFUENQV-UHFFFAOYSA-O 0.000 description 1
- HCRVPGQOAYFPQP-UHFFFAOYSA-O C/C1=[SH]/[Cu]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Cu]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Cu]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C/C1=[SH]/[Cu]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Cu]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Cu]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 HCRVPGQOAYFPQP-UHFFFAOYSA-O 0.000 description 1
- JWJNVNCJKGRDJE-UHFFFAOYSA-O C/C1=[SH]/[Cu]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Cu]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Cu]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Cu]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Cu]4(N4C=N(C)C1=C24)N7=C35 Chemical compound C/C1=[SH]/[Cu]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Cu]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Cu]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Cu]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Cu]4(N4C=N(C)C1=C24)N7=C35 JWJNVNCJKGRDJE-UHFFFAOYSA-O 0.000 description 1
- BJLZWTXHHUVHTE-UHFFFAOYSA-O C/C1=[SH]/[Cu]23C4=CC=CC5=C4N(C=C5)C4=C\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=C3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Cu]23C4=C(C=CC5=C4N(C4=C5C=CC=C4)C4=C2C2=C(C=C4)C4=C(C=CC=C4)C21)C1=C/C=C/C=C\13.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Cu]432.CN1C=C2C3=C1N(C)=CC3[Cu]13C4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C/C1=[SH]/[Cu]23C4=CC=CC5=C4N(C=C5)C4=C\2C2=C(\C=C/4)SC4=C(C=CC=C4)N2C2=C3C3=C(/C=C\2)OC2=C(C=CC=C2)P31.C1=CC2=C(C=C1)C1=C(S2)[Cu]23C4=C(C=CC5=C4N(C4=C5C=CC=C4)C4=C2C2=C(C=C4)C4=C(C=CC=C4)C21)C1=C/C=C/C=C\13.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Cu]432.CN1C=C2C3=C1N(C)=CC3[Cu]13C4=C(/C=C\C5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 BJLZWTXHHUVHTE-UHFFFAOYSA-O 0.000 description 1
- WXXMCZBQFZJQNT-UHFFFAOYSA-N C/C1=[SH]/[Cu]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=C52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C(=CS5)C5=N2C=CC=C5)C3=C14.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1CCN2C3=C1N1C4=C3[Cu]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N4CCN1C)N1=C2C=CC=C1 Chemical compound C/C1=[SH]/[Cu]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=C52)N2C4=C(C=CC=C4)C4=C2C3=C2C(=C4)CCCC21.C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C(=CS5)C5=N2C=CC=C5)C3=C14.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1CCN2C3=C1N1C4=C3[Cu]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=C63)N4CCN1C)N1=C2C=CC=C1 WXXMCZBQFZJQNT-UHFFFAOYSA-N 0.000 description 1
- SDDRLQILZCDQGH-UHFFFAOYSA-O C/C1=[SH]/[Ir]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Ir]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Ir]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C/C1=[SH]/[Ir]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Ir]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Ir]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 SDDRLQILZCDQGH-UHFFFAOYSA-O 0.000 description 1
- GUGDPBRJPYHOAR-UHFFFAOYSA-O C/C1=[SH]/[Ir]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Ir]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Ir]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Ir]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Ir]4(N4C=N(C)C1=C24)N7=C35 Chemical compound C/C1=[SH]/[Ir]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Ir]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Ir]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Ir]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Ir]4(N4C=N(C)C1=C24)N7=C35 GUGDPBRJPYHOAR-UHFFFAOYSA-O 0.000 description 1
- DPJACJXEFZAWLQ-UHFFFAOYSA-O C/C1=[SH]/[Mn]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Mn]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Mn]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Mn]45N3C=N(C)C1=C23 Chemical compound C/C1=[SH]/[Mn]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Mn]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Mn]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Mn]45N3C=N(C)C1=C23 DPJACJXEFZAWLQ-UHFFFAOYSA-O 0.000 description 1
- WOYHENMWDDXUQF-UHFFFAOYSA-O C/C1=[SH]/[Ni]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Ni]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Ni]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ni]45N3C=N(C)C1=C23 Chemical compound C/C1=[SH]/[Ni]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Ni]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Ni]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ni]45N3C=N(C)C1=C23 WOYHENMWDDXUQF-UHFFFAOYSA-O 0.000 description 1
- FAIRTDOVPCSMLU-UHFFFAOYSA-O C/C1=[SH]/[Ni]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Ni]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Ni]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Ni]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Ni]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C Chemical compound C/C1=[SH]/[Ni]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Ni]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Ni]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Ni]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Ni]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C FAIRTDOVPCSMLU-UHFFFAOYSA-O 0.000 description 1
- ZEULJDBDCUHWFE-UHFFFAOYSA-O C/C1=[SH]/[Pd]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Pd]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Pd]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pd]45N3C=N(C)C1=C23 Chemical compound C/C1=[SH]/[Pd]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Pd]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Pd]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pd]45N3C=N(C)C1=C23 ZEULJDBDCUHWFE-UHFFFAOYSA-O 0.000 description 1
- IUEPIEXQYLWXQG-UHFFFAOYSA-O C/C1=[SH]/[Pd]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Pd]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Pd]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Pd]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Pd]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C Chemical compound C/C1=[SH]/[Pd]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Pd]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Pd]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Pd]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Pd]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C IUEPIEXQYLWXQG-UHFFFAOYSA-O 0.000 description 1
- ZWXKLYLIARRHBK-UHFFFAOYSA-O C/C1=[SH]/[Pt]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Pt]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Pt]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pt]45N3C=N(C)C1=C23 Chemical compound C/C1=[SH]/[Pt]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Pt]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Pt]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pt]45N3C=N(C)C1=C23 ZWXKLYLIARRHBK-UHFFFAOYSA-O 0.000 description 1
- MOEZPDPDHAGZLO-UHFFFAOYSA-O C/C1=[SH]/[Pt]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Pt]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Pt]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Pt]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Pt]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C Chemical compound C/C1=[SH]/[Pt]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/C2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Pt]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Pt]23C2=C(/C=C\C4=C2N1C1=C(C=CC=C1)CC4)C1=N3C=CC=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Pt]312.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7C(=C35)[Pt]4(N3C=N(C)C1=C23)N1=C(C=CC=C1)N7C1=C(C=CC=C1)N6C MOEZPDPDHAGZLO-UHFFFAOYSA-O 0.000 description 1
- BEHTWBAXGGVBJY-UHFFFAOYSA-O C/C1=[SH]/[Rh]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Rh]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Rh]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C/C1=[SH]/[Rh]2(C3=C(C=CC4=C3NC3=C(C=CC=C3)S4)N3C=CC4=C3N2=CC=C4)N2=CC=CC3=C2P1C1=C(C=CC=C1)O3.C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Rh]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Rh]13/C4=C2/C=C\C2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C=C/1C1=N3OC3=C1C=CC=C3)O2.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C(C=CC5=C4C(C4=C(C=CC=C4)S5)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 BEHTWBAXGGVBJY-UHFFFAOYSA-O 0.000 description 1
- UVPFISZLBVFMJM-UHFFFAOYSA-O C/C1=[SH]/[Rh]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Rh]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Rh]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Rh]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Rh]4(N4C=N(C)C1=C24)N7=C35 Chemical compound C/C1=[SH]/[Rh]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4/N2=C2C(=C/5)\OC4=C(C=CC=C4)N1\2)N1/C=C\C2=C1N3=CC=C2.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=N6[Rh]32N2=CC=CN72)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Rh]23N2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C5C(=C4)C4=C(C=CC=C4)N5N4C5=C(C=CC=C5)C=N4[Rh]123.CN1C=C2C3=C4C(=CC=C3)N3CCN(C)N5C6=C7N(C8=C(C=CC=C8)N6C)C6=N(C=CC=C6)[Rh]4(N4C=N(C)C1=C24)N7=C35 UVPFISZLBVFMJM-UHFFFAOYSA-O 0.000 description 1
- VUECOTKSILZWNS-UHFFFAOYSA-O C/C1=[SH]/[Zn]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Zn]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Zn]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Zn]45N3C=N(C)C1=C23 Chemical compound C/C1=[SH]/[Zn]23C4=C(C=CC5=C4N(C4=C(C=CC=C4)S5)C4=C2C2=C(C=C4)OC4=C(C=CC=C4)P21)N1C=CC2=C1N3=CC=C2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=N(C=CC=C3)[Zn]54N1=C2.CN1C=C2C3=C1N(C)=CN3[Zn]13C4=C(OC5=C4/C(=C\C=C/5)C4=N1OC1=C4C=CC=C1)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)SC3=C(C=CC=C3)C6[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Zn]45N3C=N(C)C1=C23 VUECOTKSILZWNS-UHFFFAOYSA-O 0.000 description 1
- XFHHPTAFRWMOGV-UHFFFAOYSA-N C/C1=[Si](\C)[Mn]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Mn]231.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Mn]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=[Si](\C)[Mn]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Mn]231.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Mn]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 XFHHPTAFRWMOGV-UHFFFAOYSA-N 0.000 description 1
- NOEOPGKZVDUDRV-UHFFFAOYSA-N C/C1=[Si](\C)[Ni]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Ni]231.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Ni]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=[Si](\C)[Ni]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Ni]231.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Ni]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 NOEOPGKZVDUDRV-UHFFFAOYSA-N 0.000 description 1
- KGYCPPPKYHYJAR-UHFFFAOYSA-N C/C1=[Si](\C)[Pd]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Pd]231.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Pd]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=[Si](\C)[Pd]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Pd]231.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Pd]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 KGYCPPPKYHYJAR-UHFFFAOYSA-N 0.000 description 1
- ALOUFCRIKVBSSA-UHFFFAOYSA-N C/C1=[Si](\C)[Pt]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Pt]231.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Pt]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=[Si](\C)[Pt]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Pt]231.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Pt]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 ALOUFCRIKVBSSA-UHFFFAOYSA-N 0.000 description 1
- QLBDVZMQMGJQNK-UHFFFAOYSA-N C/C1=[Si](\C)[Zn]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Zn]231.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Zn]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound C/C1=[Si](\C)[Zn]23C4=CC=CC5=C4N(/C=C\5)C4=N2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2/N3=C2C(=C/4)\OC3=C(C=CC=C3)N\21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)C\5N4C(=CC5=C4C=CC=C5)[Zn]231.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4N1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1C=CC3=C1C1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6C(=C43)[Zn]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 QLBDVZMQMGJQNK-UHFFFAOYSA-N 0.000 description 1
- JIWMVBWMPIFASH-RZUXXEQNSA-N C/N=C/C=C\NC.C/N=C1\C=CC=C\C1=C\NC.CC1=CC(C2=CC=C3C(=C2)[U]C2=C3C=CC=C2)=CC(C)=C1C.CC1=CC=C(/C=C/C2=CC=CC=C2)C=C1.CC1=CC=C(C2=CC=CC=C2)C=C1.CC1=CC=C2C(=C1)[U]C1=C2C=CC=C1.CC1=C[U]C=N1C.CC1=N(C)C2=C(C=CC=C2)[U]1.CC1=N(C)C=C2C3=CC=CC=C3C3=CC=CC=C3N21.CC1=N(C)C=C[U]1.CC1=[N+](C)C2=C(C=CC=C2)N1C.CC1=[N+](C)C=CN1C.CN1C2=C(C=CC=C2)C=N1C Chemical compound C/N=C/C=C\NC.C/N=C1\C=CC=C\C1=C\NC.CC1=CC(C2=CC=C3C(=C2)[U]C2=C3C=CC=C2)=CC(C)=C1C.CC1=CC=C(/C=C/C2=CC=CC=C2)C=C1.CC1=CC=C(C2=CC=CC=C2)C=C1.CC1=CC=C2C(=C1)[U]C1=C2C=CC=C1.CC1=C[U]C=N1C.CC1=N(C)C2=C(C=CC=C2)[U]1.CC1=N(C)C=C2C3=CC=CC=C3C3=CC=CC=C3N21.CC1=N(C)C=C[U]1.CC1=[N+](C)C2=C(C=CC=C2)N1C.CC1=[N+](C)C=CN1C.CN1C2=C(C=CC=C2)C=N1C JIWMVBWMPIFASH-RZUXXEQNSA-N 0.000 description 1
- WPWCZDCDKIRDOB-VGSRZYFESA-N C/N=C1\C=CC=C\C1=C\NC.CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=N(C)C=C[U]1.CC1=[N+](C)C=CN1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CN/C(C)=C\C=C/[U].CN1C=CC=N1C.CN1C=[U]C=N1C Chemical compound C/N=C1\C=CC=C\C1=C\NC.CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=N(C)C=C[U]1.CC1=[N+](C)C=CN1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CN/C(C)=C\C=C/[U].CN1C=CC=N1C.CN1C=[U]C=N1C WPWCZDCDKIRDOB-VGSRZYFESA-N 0.000 description 1
- RURXDGNUFCWRGR-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(/C=C3C4=C/1N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C\4(C1CCCC\31)N1=C3C(=CC=C1)C1=C(C=CC=C1)N63)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=C3C(=C/1)\C1CCCC1C\31C3=C4C(=CC=C3N3C5=C(C=CC=C5)C5=CC=CN1=C53)C1=C(C=CC=C1)N42.C1=CC2=C(C=C1)C1=C/C3=C4C(=C/1[U]2)/C1CCCC1C/41C2=C4C(=CC=C2N2C5=C(C=CC=C5)C5=CC=CN1=C52)C1=C(C=CC=C1)N43 Chemical compound C1=CC2=C(C=C1)C1=C(/C=C3C4=C/1N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C\4(C1CCCC\31)N1=C3C(=CC=C1)C1=C(C=CC=C1)N63)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=C3C(=C/1)\C1CCCC1C\31C3=C4C(=CC=C3N3C5=C(C=CC=C5)C5=CC=CN1=C53)C1=C(C=CC=C1)N42.C1=CC2=C(C=C1)C1=C/C3=C4C(=C/1[U]2)/C1CCCC1C/41C2=C4C(=CC=C2N2C5=C(C=CC=C5)C5=CC=CN1=C52)C1=C(C=CC=C1)N43 RURXDGNUFCWRGR-UHFFFAOYSA-N 0.000 description 1
- UUWKWHHAMPHPAU-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(/C=C3C4=C/1N1C5=C(C=CC=C5)C5=CC=C6N7C8=C(C=CC=C8)C8=CC=CN(=C87)C\4(C4CCCC\34)N6=C51)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=C3C(=C/1)\C1CCCC1C\31N3=C4C(=CC=C3)C3=C(C=CC=C3)N4C3=CC=C4C5=C(C=CC=C5)N2C4=N31.C1=CC2=C(C=C1)C1=C/C3=C4C(=C/1[U]2)/C1CCCC1C/41N2=C4C(=CC=C2)C2=C(C=CC=C2)N4C2=CC=C4C5=C(C=CC=C5)N3C4=N21 Chemical compound C1=CC2=C(C=C1)C1=C(/C=C3C4=C/1N1C5=C(C=CC=C5)C5=CC=C6N7C8=C(C=CC=C8)C8=CC=CN(=C87)C\4(C4CCCC\34)N6=C51)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=C3C(=C/1)\C1CCCC1C\31N3=C4C(=CC=C3)C3=C(C=CC=C3)N4C3=CC=C4C5=C(C=CC=C5)N2C4=N31.C1=CC2=C(C=C1)C1=C/C3=C4C(=C/1[U]2)/C1CCCC1C/41N2=C4C(=CC=C2)C2=C(C=CC=C2)N4C2=CC=C4C5=C(C=CC=C5)N3C4=N21 UUWKWHHAMPHPAU-UHFFFAOYSA-N 0.000 description 1
- QQJNWCJSDVCCKB-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(/C=C3C4=C/1N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C\4(C1=C4C(=CC=C1)C1=C(C=CC=C1)N4\3)C1CCCC/61)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=C3C(=C/1)\N1C4=C(C=CC=C4)C4=CC=CC(=C41)C\31C3=C4C(=C\C=C/3C3CCCC31)/C1=C(C=CC=C1)N/42.C1=CC2=C(C=C1)C1=C3C4=C(/C=C/1[U]2)N1C2=C(C=CC=C2)C2=C\C=C5C(=C/21)/C\4(C1=C2C(=CC=C1)C1=C(C=CC=C1)N2/3)C1CCCC/51.C1=CC2=C(C=C1)N1C3=CC=CC4=C3C3(C5=C1C2=CC=C5)C1=C2C(=C\C=C/1C1CCCC13)/C1=C(C=CC=C1)N4/2 Chemical compound C1=CC2=C(C=C1)C1=C(/C=C3C4=C/1N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C\4(C1=C4C(=CC=C1)C1=C(C=CC=C1)N4\3)C1CCCC/61)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=C3C(=C/1)\N1C4=C(C=CC=C4)C4=CC=CC(=C41)C\31C3=C4C(=C\C=C/3C3CCCC31)/C1=C(C=CC=C1)N/42.C1=CC2=C(C=C1)C1=C3C4=C(/C=C/1[U]2)N1C2=C(C=CC=C2)C2=C\C=C5C(=C/21)/C\4(C1=C2C(=CC=C1)C1=C(C=CC=C1)N2/3)C1CCCC/51.C1=CC2=C(C=C1)N1C3=CC=CC4=C3C3(C5=C1C2=CC=C5)C1=C2C(=C\C=C/1C1CCCC13)/C1=C(C=CC=C1)N4/2 QQJNWCJSDVCCKB-UHFFFAOYSA-N 0.000 description 1
- ABCTZJWXUDZIGZ-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(/C=C3N4C5=C(C=CC=C5)C5=CC=CN(=C54)C45C6=C7C(=C\C=C/6C6CCCC64)\C4=C(/C=C\C=C/4)N\7/C1=N/35)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=N3C(=C/1)\N1C4=C(C=CC=C4)C4=CC=CN(=C41)C\31C3=C4C(=C\C=C/3C3CCCC31)/C1=C(/C=C\C=C/1)N/42.C1=CC2=C(C=C1)N1C3=N(C=CC=C23)C23C4=C5C(=C\C=C/4C4CCCC42)/C2=C(/C=C\C=C/2)N/5C2=N3/C1=C/C=C\2.C1=CC=C2C(=C1)C1=C3N2C2=N(/C=C4/C5=C(C=CC=C5)[U]/C4=C/2)C24C5=C6C(=C\C=C/5C5CCCC52)/C2=C(/C=C\C=C/2)N/6C(=N/34)/C=C\1.C1=CC=C2C(=C1)C1=C3N2C2=N(/C=C4/[U]C5=C(C=CC=C5)/C4=C/2)C24C5=C6C(=C\C=C/5C5CCCC52)/C2=C(/C=C\C=C/2)N/6C(=N/34)/C=C\1 Chemical compound C1=CC2=C(C=C1)C1=C(/C=C3N4C5=C(C=CC=C5)C5=CC=CN(=C54)C45C6=C7C(=C\C=C/6C6CCCC64)\C4=C(/C=C\C=C/4)N\7/C1=N/35)[U]2.C1=CC2=C(C=C1)C1=C([U]2)/C2=N3C(=C/1)\N1C4=C(C=CC=C4)C4=CC=CN(=C41)C\31C3=C4C(=C\C=C/3C3CCCC31)/C1=C(/C=C\C=C/1)N/42.C1=CC2=C(C=C1)N1C3=N(C=CC=C23)C23C4=C5C(=C\C=C/4C4CCCC42)/C2=C(/C=C\C=C/2)N/5C2=N3/C1=C/C=C\2.C1=CC=C2C(=C1)C1=C3N2C2=N(/C=C4/C5=C(C=CC=C5)[U]/C4=C/2)C24C5=C6C(=C\C=C/5C5CCCC52)/C2=C(/C=C\C=C/2)N/6C(=N/34)/C=C\1.C1=CC=C2C(=C1)C1=C3N2C2=N(/C=C4/[U]C5=C(C=CC=C5)/C4=C/2)C24C5=C6C(=C\C=C/5C5CCCC52)/C2=C(/C=C\C=C/2)N/6C(=N/34)/C=C\1 ABCTZJWXUDZIGZ-UHFFFAOYSA-N 0.000 description 1
- RDKWYQQNMFAJFQ-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=C/C=C6C(=C/51)/C4(C1=C4/C(=C\C=C/1)C1=C(C=CC=C1)N4/6)C1CCCC31)[U]2.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C/C5=C(\C=C/1C41C4=C(/C=C/C=C/4C4CCCC41)N23)C1=C(C=CC=C1)[U]5.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5\C6=C(C=CC=C6)[U]\C5=C\C=C\1C41C4=C(/C=C\C=C/4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=C1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)[U]C1=C2/C=C2C(=C/1)\C13C4=C5C(=CC6=C4N(C4=CC=CC=C46)C4=C1/C(=C\C=C/4)C1CCCC13)C1=C(C=CC=C1)N5\2 Chemical compound C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=C/C=C6C(=C/51)/C4(C1=C4/C(=C\C=C/1)C1=C(C=CC=C1)N4/6)C1CCCC31)[U]2.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C/C5=C(\C=C/1C41C4=C(/C=C/C=C/4C4CCCC41)N23)C1=C(C=CC=C1)[U]5.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5\C6=C(C=CC=C6)[U]\C5=C\C=C\1C41C4=C(/C=C\C=C/4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=C1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)[U]C1=C2/C=C2C(=C/1)\C13C4=C5C(=CC6=C4N(C4=CC=CC=C46)C4=C1/C(=C\C=C/4)C1CCCC13)C1=C(C=CC=C1)N5\2 RDKWYQQNMFAJFQ-UHFFFAOYSA-N 0.000 description 1
- XPRQCYDCIYAVFA-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=C/C=C6C(=C/51)/C4(C1CCCC31)N1=C3C(=CC=C1)C1=C(C=CC=C1)N3/6)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)C1CCCC1C31C3=C4C(=C/C=C/3N3C5=C(C=CC=C5)C5=CC=CN1=C53)/C1=C(C=CC=C1)N2/4.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)C1CCCC1C41C2=C4C(=C/C=C/2N2C5=C(C=CC=C5)C5=CC=CN1=C52)/C1=C(C=CC=C1)N3/4.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=N1C41C4=C(C=CC=C4C4CCCC41)N23 Chemical compound C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=C/C=C6C(=C/51)/C4(C1CCCC31)N1=C3C(=CC=C1)C1=C(C=CC=C1)N3/6)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)C1CCCC1C31C3=C4C(=C/C=C/3N3C5=C(C=CC=C5)C5=CC=CN1=C53)/C1=C(C=CC=C1)N2/4.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)C1CCCC1C41C2=C4C(=C/C=C/2N2C5=C(C=CC=C5)C5=CC=CN1=C52)/C1=C(C=CC=C1)N3/4.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=N1C41C4=C(C=CC=C4C4CCCC41)N23 XPRQCYDCIYAVFA-UHFFFAOYSA-N 0.000 description 1
- MICLJGKFELAWHK-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=C1C1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)C14C1CCCC31)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)C1CCCC1C3C1=CC=CC3=C1N(C1=CC4=C(C=C1)C1=C(C=CC=C1)N42)C1=C3C=CC=C1.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=C1C41C4=C(C=CC=C4C4CCCC41)N23.CC.CC.CC Chemical compound C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=C1C1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)C14C1CCCC31)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)C1CCCC1C3C1=CC=CC3=C1N(C1=CC4=C(C=C1)C1=C(C=CC=C1)N42)C1=C3C=CC=C1.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=C1C41C4=C(C=CC=C4C4CCCC41)N23.CC.CC.CC MICLJGKFELAWHK-UHFFFAOYSA-N 0.000 description 1
- QHKGRCFUQVMENU-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC=CC4=C1N3C1=C4C=CC=C1)C1CCCC61)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)N1C4=C(C=CC=C4)C4=C1C(=CC=C4)C31C3=C4C(=CC=C3C3CCCC31)C1=C(C=CC=C1)N42.C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=CC=C5C(=C21)C4(C1=CC=CC2=C1N3C1=C2C=CC=C1)C1CCCC51.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)N1C2=C(C=CC=C2)C2=C1C(=CC=C2)C41C2=C4C(=CC=C2C2CCCC21)C1=C(C=CC=C1)N34.CC.CC.CC.CC Chemical compound C1=CC2=C(C=C1)C1=C(C=C3C4=C1N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC=CC4=C1N3C1=C4C=CC=C1)C1CCCC61)[U]2.C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)N1C4=C(C=CC=C4)C4=C1C(=CC=C4)C31C3=C4C(=CC=C3C3CCCC31)C1=C(C=CC=C1)N42.C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=CC=C5C(=C21)C4(C1=CC=CC2=C1N3C1=C2C=CC=C1)C1CCCC51.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)N1C2=C(C=CC=C2)C2=C1C(=CC=C2)C41C2=C4C(=CC=C2C2CCCC21)C1=C(C=CC=C1)N34.CC.CC.CC.CC QHKGRCFUQVMENU-UHFFFAOYSA-N 0.000 description 1
- YIOOAANPPYIZSJ-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)C1CCCC1C31C3=C4/C(=C\C=C/3)C3=C(C=CC=C3)N4C3=C\C=C4\C5=C(C=CC=C5)N2\C4=C\31.C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=C/C=C5C(=C/21)/C4(C1=C2/C(=C\C=C/1)C1=C(C=CC=C1)N2/5)C1CCCC31.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)C1CCCC1C41C2=C4/C(=C\C=C/2)C2=C(C=CC=C2)N4C2=C\C=C4\C5=C(C=CC=C5)N3\C4=C\21 Chemical compound C1=CC2=C(C=C1)C1=C([U]2)C2=C3C(=C1)C1CCCC1C31C3=C4/C(=C\C=C/3)C3=C(C=CC=C3)N4C3=C\C=C4\C5=C(C=CC=C5)N2\C4=C\31.C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=C/C=C5C(=C/21)/C4(C1=C2/C(=C\C=C/1)C1=C(C=CC=C1)N2/5)C1CCCC31.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)C1CCCC1C41C2=C4/C(=C\C=C/2)C2=C(C=CC=C2)N4C2=C\C=C4\C5=C(C=CC=C5)N3\C4=C\21 YIOOAANPPYIZSJ-UHFFFAOYSA-N 0.000 description 1
- BJMDUITVKDUHGL-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=C1C1=C(C=C2)N2C5=C(C=CC=C5)C5=C2C(=CC=C5)C41C1CCCC31.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)C1CCCC1C41C2=CC=CC4=C2N(C2=C4C=CC=C2)C2=C1C1=C(C=C2)C2=C(C=CC=C2)N31.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3CCCC3C54C3=CC=CC2=C31.CC.CC.CC Chemical compound C1=CC2=C(C=C1)C1=C3C4=C(C=C1[U]2)N1C2=C(C=CC=C2)C2=C1C1=C(C=C2)N2C5=C(C=CC=C5)C5=C2C(=CC=C5)C41C1CCCC31.C1=CC2=C(C=C1)C1=CC3=C4C(=C1[U]2)C1CCCC1C41C2=CC=CC4=C2N(C2=C4C=CC=C2)C2=C1C1=C(C=C2)C2=C(C=CC=C2)N31.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3CCCC3C54C3=CC=CC2=C31.CC.CC.CC BJMDUITVKDUHGL-UHFFFAOYSA-N 0.000 description 1
- KWPXMJXYFOTGIR-UHFFFAOYSA-N C1=CC2=C(C=C1)C1=C3C4=C(\C=C/1[U]2)N1C2=C(C=CC=C2)C2=CC=C5N6C7=C(C=CC=C7)C7=CC=CN(=C76)C/4(C4CCCC/34)N5=C21.C1=CC2=C(C=C1)C1=C3N4C5=C(C=CC=C5)/C5=C/C=C\N(=C54)C45C6=C7C(=C\C=C/6C6CCCC64)/C4=C(/C=C\C=C/4)N/7C(=N/35)/C=C\1[U]2.C1=CC2=C(C=C1)C1=C\C3=N4C(=C/1[U]2)/N1C2=C(C=CC=C2)/C2=C/C=C\N(=C21)C/41C2=C4C(=C\C=C/2C2CCCC21)/C1=C(/C=C\C=C/1)N/43.C1=CC2=C(C=C1)N1C3=CC=C4C5=C(C=CC=C5)N5C4=N3C3(C4=C5/C=C/C=C\4C4CCCC43)N3=C1C2=CC=C3 Chemical compound C1=CC2=C(C=C1)C1=C3C4=C(\C=C/1[U]2)N1C2=C(C=CC=C2)C2=CC=C5N6C7=C(C=CC=C7)C7=CC=CN(=C76)C/4(C4CCCC/34)N5=C21.C1=CC2=C(C=C1)C1=C3N4C5=C(C=CC=C5)/C5=C/C=C\N(=C54)C45C6=C7C(=C\C=C/6C6CCCC64)/C4=C(/C=C\C=C/4)N/7C(=N/35)/C=C\1[U]2.C1=CC2=C(C=C1)C1=C\C3=N4C(=C/1[U]2)/N1C2=C(C=CC=C2)/C2=C/C=C\N(=C21)C/41C2=C4C(=C\C=C/2C2CCCC21)/C1=C(/C=C\C=C/1)N/43.C1=CC2=C(C=C1)N1C3=CC=C4C5=C(C=CC=C5)N5C4=N3C3(C4=C5/C=C/C=C\4C4CCCC43)N3=C1C2=CC=C3 KWPXMJXYFOTGIR-UHFFFAOYSA-N 0.000 description 1
- DAXCLQLOXWGICG-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C(C=CC=C4)/C4=C/SC5=C4N2=C2N(C4=CC=CC1=C43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Ag]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=C/C6=C7C(=CO6)C6=C(C=CC=C6)[Ag]4(C4/C=N(/C)C1=C24)\N7=C\53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C(C=CC=C4)/C4=C/SC5=C4N2=C2N(C4=CC=CC1=C43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Ag]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=C/C6=C7C(=CO6)C6=C(C=CC=C6)[Ag]4(C4/C=N(/C)C1=C24)\N7=C\53 DAXCLQLOXWGICG-UHFFFAOYSA-N 0.000 description 1
- BOVMXMMPICSZAN-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C(C=CC=C4)N4CC/C5=C4/C4=C(\S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=C62)\C5=N\43.C1=CC=C(/C2=[SiH]/[Ag]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=CC=C6C=CC=C2C6=C53)C2=CC=CC3=C2N4=CC=C3)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Ag]3(C5C=N(C)C6=C5/C4=C\C=C/6)/N4=C5C(=C/C1=C/24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CC=CC=C3[Ag]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C(C=CC=C4)N4CC/C5=C4/C4=C(\S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=C62)\C5=N\43.C1=CC=C(/C2=[SiH]/[Ag]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=CC=C6C=CC=C2C6=C53)C2=CC=CC3=C2N4=CC=C3)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Ag]3(C5C=N(C)C6=C5/C4=C\C=C/6)/N4=C5C(=C/C1=C/24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CC=CC=C3[Ag]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 BOVMXMMPICSZAN-UHFFFAOYSA-N 0.000 description 1
- JMKCITGKWFBYBR-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C6=C(CCN6C6=N2C=CC=C6)S5)C3=C14.C1=CC=C(S2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Ag]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Ag]2(C2=CC=CC=C27)C3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Ag]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C6=C(CCN6C6=N2C=CC=C6)S5)C3=C14.C1=CC=C(S2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Ag]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Ag]2(C2=CC=CC=C27)C3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Ag]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1 JMKCITGKWFBYBR-UHFFFAOYSA-O 0.000 description 1
- RNDNCLMFZGNFHN-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2C3=C1C=C4.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3C(=CS5)[Ag]43C4=C/C=C/C=C\4C4=N3C1=C2C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(/C=C5/C6=C(C=CC=C6)N6/C5=N/3[Ag]23C2=CC=CC=C2C2=C3C3=C(C=C2)O/C=C\36)S4)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ag]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2C3=C1C=C4.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3C(=CS5)[Ag]43C4=C/C=C/C=C\4C4=N3C1=C2C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(/C=C5/C6=C(C=CC=C6)N6/C5=N/3[Ag]23C2=CC=CC=C2C2=C3C3=C(C=C2)O/C=C\36)S4)C=C1 RNDNCLMFZGNFHN-UHFFFAOYSA-N 0.000 description 1
- RFNJUPILEOCZLS-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4)/C4=C/SC5=C4N2=C2N(C4=CC=CC1=C43)C1=C(C=CC=C1)N52.CC1=N[Au]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2C3=C2/C(=C\4)CCCC12.CN1CCN2C3=C(C=CC=C3)[Au]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)/C=C\C(=C63)N3CCN(C)N5C1=C2N4=C35 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4)/C4=C/SC5=C4N2=C2N(C4=CC=CC1=C43)C1=C(C=CC=C1)N52.CC1=N[Au]23C4=CC=CC=C4C4=C5C(=CC=C4)OC(=N52)N2C4=C(C=CC=C4)C4=C2C3=C2/C(=C\4)CCCC12.CN1CCN2C3=C(C=CC=C3)[Au]34C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)/C=C\C(=C63)N3CCN(C)N5C1=C2N4=C35 RFNJUPILEOCZLS-UHFFFAOYSA-N 0.000 description 1
- FBYBHNCTHOGONG-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4)N4CC/C5=C4/C4=C(\S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=C62)\C5=N\43.C1=CC=C(/C2=[SiH]/[Au]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=CC=C6C=CC=C2C6=C53)C2=CC=CC3=C2N4=CC=C3)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Au]3(C5C=N(C)C6=C5/C4=C\C=C/6)/N4=C5C(=C/C1=C/24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4)N4CC/C5=C4/C4=C(\S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=C62)\C5=N\43.C1=CC=C(/C2=[SiH]/[Au]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=CC=C6C=CC=C2C6=C53)C2=CC=CC3=C2N4=CC=C3)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Au]3(C5C=N(C)C6=C5/C4=C\C=C/6)/N4=C5C(=C/C1=C/24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 FBYBHNCTHOGONG-UHFFFAOYSA-N 0.000 description 1
- ITACPHPKQHBHNI-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4N2=C2C(=C5)C4=C(C=CC=C4)N21)C1=C/C=C/C=C\13.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5N(C6=CC=CC7=N6[Au]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Au]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C(C=CC=C4N4C5=C(C=CC=C5)C5=C4N2=C2C(=C5)C4=C(C=CC=C4)N21)C1=C/C=C/C=C\13.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5N(C6=CC=CC7=N6[Au]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Au]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13 ITACPHPKQHBHNI-UHFFFAOYSA-N 0.000 description 1
- KICKIWNIELBNIT-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C6=C(CCN6C6=N2C=CC=C6)S5)C3=C14.C1=CC=C(S2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Au]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Au]2(C2=CC=CC=C27)C3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Au]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C6=C(CCN6C6=N2C=CC=C6)S5)C3=C14.C1=CC=C(S2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Au]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Au]2(C2=CC=CC=C27)C3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Au]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1 KICKIWNIELBNIT-UHFFFAOYSA-O 0.000 description 1
- BYHKIFAITDZSQI-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2C3=C1C=C4.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3C(=CS5)[Au]43C4=C/C=C/C=C\4C4=N3C1=C2C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(/C=C5/C6=C(C=CC=C6)N6/C5=N/3[Au]23C2=CC=CC=C2C2=C3C3=C(C=C2)O/C=C\36)S4)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Au]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2C3=C1C=C4.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3C(=CS5)[Au]43C4=C/C=C/C=C\4C4=N3C1=C2C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(/C=C5/C6=C(C=CC=C6)N6/C5=N/3[Au]23C2=CC=CC=C2C2=C3C3=C(C=C2)O/C=C\36)S4)C=C1 BYHKIFAITDZSQI-UHFFFAOYSA-N 0.000 description 1
- HTZKJQSTNCTVBE-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Co]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Co]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Co]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Co]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Co]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Co]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Co]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Co]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 HTZKJQSTNCTVBE-UHFFFAOYSA-N 0.000 description 1
- DROWVDZGMULYOR-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Co]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Co]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Co]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C[SH]1C2=C3C4=C1C1=C(C=CC=C1)N4[Ge](C1=CC=CC=C1)(C1=CC=CC=C1)[Co]14N5=CC=CC=C5C5=N1C1=C(C=C5)O/C=C\1N1C5=C(C=CC=C5)C(=C2)C1=N34 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Co]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Co]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Co]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C[SH]1C2=C3C4=C1C1=C(C=CC=C1)N4[Ge](C1=CC=CC=C1)(C1=CC=CC=C1)[Co]14N5=CC=CC=C5C5=N1C1=C(C=C5)O/C=C\1N1C5=C(C=CC=C5)C(=C2)C1=N34 DROWVDZGMULYOR-UHFFFAOYSA-N 0.000 description 1
- SFLDONWDMYWEIH-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Cu]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Cu]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Cu]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Cu]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Cu]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Cu]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Cu]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Cu]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 SFLDONWDMYWEIH-UHFFFAOYSA-N 0.000 description 1
- NUJGUQMNPZEMDS-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C(C=CC=C4)/C4=C/SC5=C4N2=C2N(C4=CC=CC1=C43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Cu]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=C/C6=C7C(=CO6)C6=C(C=CC=C6)[Cu]4(C4/C=N(/C)C1=C24)\N7=C\53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C(C=CC=C4)/C4=C/SC5=C4N2=C2N(C4=CC=CC1=C43)C1=C(C=CC=C1)N52.C1=CC=C(N2C3=CC=CC4=N3[Cu]3(C5=CC=CC=C54)C4=C2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=C/C6=C7C(=CO6)C6=C(C=CC=C6)[Cu]4(C4/C=N(/C)C1=C24)\N7=C\53 NUJGUQMNPZEMDS-UHFFFAOYSA-N 0.000 description 1
- PCVPHBZFESGUJN-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C(C=CC=C4)N4CC/C5=C4/C4=C(\S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=C62)\C5=N\43.C1=CC=C(/C2=[SiH]/[Cu]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=CC=C6C=CC=C2C6=C53)C2=CC=CC3=C2N4=CC=C3)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Cu]3(C5C=N(C)C6=C5/C4=C\C=C/6)/N4=C5C(=C/C1=C/24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CC=CC=C3[Cu]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C(C=CC=C4)N4CC/C5=C4/C4=C(\S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=C62)\C5=N\43.C1=CC=C(/C2=[SiH]/[Cu]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=CC=C6C=CC=C2C6=C53)C2=CC=CC3=C2N4=CC=C3)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Cu]3(C5C=N(C)C6=C5/C4=C\C=C/6)/N4=C5C(=C/C1=C/24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CC=CC=C3[Cu]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 PCVPHBZFESGUJN-UHFFFAOYSA-N 0.000 description 1
- CVSMJOGNSIOANQ-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C6=C(CCN6C6=N2C=CC=C6)S5)C3=C14.C1=CC=C(S2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Cu]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Cu]2(C2=CC=CC=C27)C3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Cu]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=C1C=CC=C4N1C4=C(C=CC=C4)N4C5=C(C6=C(CCN6C6=N2C=CC=C6)S5)C3=C14.C1=CC=C(S2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Cu]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Cu]2(C2=CC=CC=C27)C3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Cu]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1 CVSMJOGNSIOANQ-UHFFFAOYSA-O 0.000 description 1
- RVWRIEVNJKXQSD-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2C3=C1C=C4.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3C(=CS5)[Cu]43C4=C/C=C/C=C\4C4=N3C1=C2C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(/C=C5/C6=C(C=CC=C6)N6/C5=N/3[Cu]23C2=CC=CC=C2C2=C3C3=C(C=C2)O/C=C\36)S4)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Cu]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2C3=C1C=C4.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3C(=CS5)[Cu]43C4=C/C=C/C=C\4C4=N3C1=C2C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(/C=C5/C6=C(C=CC=C6)N6/C5=N/3[Cu]23C2=CC=CC=C2C2=C3C3=C(C=C2)O/C=C\36)S4)C=C1 RVWRIEVNJKXQSD-UHFFFAOYSA-N 0.000 description 1
- YXPLCEGRIMHMBD-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Cu]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=N3[Cu]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Cu]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Cu]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Cu]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=N3[Cu]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Cu]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Cu]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 YXPLCEGRIMHMBD-UHFFFAOYSA-N 0.000 description 1
- GRJNIYUIGRGOHD-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Ir]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Ir]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Ir]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Ir]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ir]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Ir]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Ir]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Ir]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 GRJNIYUIGRGOHD-UHFFFAOYSA-N 0.000 description 1
- ASYRUGQNKQZFLW-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Ir]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=N3[Ir]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Ir]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Ir]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ir]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=N3[Ir]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Ir]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Ir]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 ASYRUGQNKQZFLW-UHFFFAOYSA-N 0.000 description 1
- ODYXRCVBQAQRPQ-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Mn]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Mn]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=C(C5=CC=CC6=C5N1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Mn]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Mn]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=C(C5=CC=CC6=C5N1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 ODYXRCVBQAQRPQ-UHFFFAOYSA-O 0.000 description 1
- FYCXCZWVTNTQRR-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Mn]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Mn]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Mn]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Mn]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Mn]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Mn]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 FYCXCZWVTNTQRR-UHFFFAOYSA-O 0.000 description 1
- KKSDHBDKVMPAJH-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Mn]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Mn]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Mn]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Mn]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Mn]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 KKSDHBDKVMPAJH-UHFFFAOYSA-N 0.000 description 1
- RNOAYRQQUHMIKQ-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Ni]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Ni]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=C(C5=CC=CC6=C5N1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Ni]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Ni]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=C(C5=CC=CC6=C5N1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 RNOAYRQQUHMIKQ-UHFFFAOYSA-O 0.000 description 1
- XDJPHHNKOVTSFW-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Ni]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Ni]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Pt]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Ni]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Ni]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Pt]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 XDJPHHNKOVTSFW-UHFFFAOYSA-O 0.000 description 1
- GCXDIIGMJJHYBY-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Ni]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Ni]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Ni]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Ni]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Ni]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 GCXDIIGMJJHYBY-UHFFFAOYSA-N 0.000 description 1
- YWPCUYLENXKXGT-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Pd]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Pd]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=C(C5=CC=CC6=C5C1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Pd]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Pd]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=C(C5=CC=CC6=C5C1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 YWPCUYLENXKXGT-UHFFFAOYSA-O 0.000 description 1
- DLFQYSRAYREEGY-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Pd]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Pd]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Pd]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Pd]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Pd]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Pd]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 DLFQYSRAYREEGY-UHFFFAOYSA-O 0.000 description 1
- ITMPUPGBPPLVRD-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Pd]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Pd]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Pd]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Pd]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Pd]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 ITMPUPGBPPLVRD-UHFFFAOYSA-N 0.000 description 1
- IVFQBKOITOOLKW-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Pt]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Pt]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=C(C5=CC=CC6=C5C1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Pt]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Pt]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=C(C5=CC=CC6=C5C1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 IVFQBKOITOOLKW-UHFFFAOYSA-O 0.000 description 1
- AGBOTBAMZIMGRM-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Pt]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Pt]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Pt]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Pt]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Pt]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Pt]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 AGBOTBAMZIMGRM-UHFFFAOYSA-O 0.000 description 1
- QCXAXSHCMWWPIN-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Pt]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Pt]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Pt]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Pt]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Pt]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 QCXAXSHCMWWPIN-UHFFFAOYSA-N 0.000 description 1
- GLAOFNRWRBHIMU-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Rh]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Rh]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Rh]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Rh]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Rh]2(N3=C(C=CC=C3)C3=CSC4=C3N2=C2NC3=C(C=CC=C3)N42)N2=C1C=CC=C2.C1=CC=C(N2C3=CC=CC4=N3[Rh]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CC3[Rh]13N4=C(C=CC=C4)C4=COC5=C4N1=C1C(=C5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Rh]34N5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 GLAOFNRWRBHIMU-UHFFFAOYSA-N 0.000 description 1
- NFVFBVBZGMHYQK-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Rh]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=N3[Rh]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Rh]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Rh]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Rh]23N4=CC=CC5=C4N(C=C5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=N3[Rh]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Rh]23N2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Rh]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 NFVFBVBZGMHYQK-UHFFFAOYSA-N 0.000 description 1
- XGIJEQCQWWNEHC-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Zn]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Zn]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=C(C5=CC=CC6=C5N1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=C(C=CC=C4)C4=COC5=C4N2=C(C=C5)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC=C(/C2=[SH]/[Zn]34/C5=C/C=C\C6=C5C(=CC=C6)C5=N3C3=C(C=C5)CCC5=C(/C=C\C=C/5)N3C3=N4C4=C(OC=C42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Zn]432)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=C(C5=CC=CC6=C5N1=C(O6)N1C5=C(C=CC=C5)N(C)C5=C1N3=C2C=C5)C1=C(C=CC=C1)O4 XGIJEQCQWWNEHC-UHFFFAOYSA-O 0.000 description 1
- WPBCHRNJMPRJAV-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Zn]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Zn]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Zn]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=C(C=CC=C4)N4CCC5=C4C4=C(S5)N5C6=C(C=CC=C6)N(C6=CC=CC1=N62)C5=N43.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C(/C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Zn]2(C2=CC=CC=C27)N3=C54)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Zn]23C2=CC=CC=C2C2=N3C3=C(C=CC=C34)C=C2)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Zn]52C2=CC=CC3=C2/C4=C\C=C/3)C=C1 WPBCHRNJMPRJAV-UHFFFAOYSA-O 0.000 description 1
- FCNIGPMSFOOBRO-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Zn]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Zn]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 Chemical compound C1=CC2=C(C=C1)N1C(=C2)[Zn]23C4=CC=CC5=C4N(/C=C\5)C4=CC=CC(=N42)N2C4=C(C=CC=C4)C4=C2N3=C1C=C4.C1=CC2=C(C=C1)N1C3=C(C=CC4=N3[Zn]3(C5=C(C=CC=C5)C5=CC=CC1=N53)/C1=C/C=C\C3=C1N4C=C3)S2.C1=CC2=C(C=C1)N1C3=C2C=CC2=N3[Zn]3(C4=CSC5=C4C(=CS5)C4=CC=CC1=N43)/C1=C/C=C/C=C\21.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=CSC5=C4C(=CC=C5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1N3=C2C=C4 FCNIGPMSFOOBRO-UHFFFAOYSA-N 0.000 description 1
- PTLFLYBZRJWHHK-UHFFFAOYSA-P C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Ni]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Ni]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Ni]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Ni]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Ni]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Ni]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Ni]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Ni]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 PTLFLYBZRJWHHK-UHFFFAOYSA-P 0.000 description 1
- BIJVRPVOTWNWFJ-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Ni]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Ni]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Ni]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Ni]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Ni]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Ni]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Ni]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Ni]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 BIJVRPVOTWNWFJ-UHFFFAOYSA-N 0.000 description 1
- IFYZMIUGISBJMZ-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pd]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Pd]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([Pd]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Pt]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Pd]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pd]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Pd]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([Pd]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Pt]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Pd]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 IFYZMIUGISBJMZ-UHFFFAOYSA-O 0.000 description 1
- CHQMLBMITMYJFH-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pd]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Pd]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Pd]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Pd]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pd]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Pd]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Pd]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Pd]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 CHQMLBMITMYJFH-UHFFFAOYSA-N 0.000 description 1
- XQJMVXLGTSLMGC-UHFFFAOYSA-P C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pt]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Pt]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Pt]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Pt]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pt]3(/C4=C5\NC6=C(C=CC=C6)N5C5=C4C4=C(CCN4C4=N3C=CC=C4)S5)N1=C2.C1=CC=C(/C2=[SH]/[Pt]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Pt]2(C3=C54)N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Pt]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 XQJMVXLGTSLMGC-UHFFFAOYSA-P 0.000 description 1
- OSQBJESPAIEPNA-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pt]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Pt]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Pt]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Pt]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=C(C=CC=C3)[Pt]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Pt]3(C5=C2SC2=C5C(=CC=C2)C2=N3C3=C(C=CC=C3)C=C2)N2=CC=CC=C42)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=N(C=CC=C6)[Pt]4(C7=C53)N3C=N(C)C1=C23.CN1C=C2C3=CC=CC=N3[Pt]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2C3=C65)N1C=CC2=C1N4=CC=C2 OSQBJESPAIEPNA-UHFFFAOYSA-N 0.000 description 1
- MOMUQMFMBVXXOO-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C2/C=C\C2=C/3C3(/C4=C1/C=C\C1=C4C4=C(/C=C\C=N/43)[U]1)C1CCCC21.C1=CC2=C(C=C1)N1C3=N(C=CC=C23)C23/C4=C1/C=C\C1=C4C4=C2/C(=C/C=C/4[U]1)C1CCCC13 Chemical compound C1=CC2=C(C=C1)N1C3=C2/C=C\C2=C/3C3(/C4=C1/C=C\C1=C4C4=C(/C=C\C=N/43)[U]1)C1CCCC21.C1=CC2=C(C=C1)N1C3=N(C=CC=C23)C23/C4=C1/C=C\C1=C4C4=C2/C(=C/C=C/4[U]1)C1CCCC13 MOMUQMFMBVXXOO-UHFFFAOYSA-N 0.000 description 1
- LLANOFWOQAVQJS-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C2/C=C\C2=C/3[Pd]3(C4=C5C(=CC=C4C4=N3C=CC=C4)C3=C(C=CC=C3)N52)N2=C1C=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=C2/C=C\C2=C/3[Pd]3(C4=C5C(=CC=C4C4=N3C=CC=C4)C3=C(C=CC=C3)N52)N2=C1C=CC=C2 LLANOFWOQAVQJS-UHFFFAOYSA-N 0.000 description 1
- SOZMONMCPLPWME-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3N(=CS5)[Ag]43C4=C(C=CC2=C41)C1=C/C=C/C=C\13.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=N(C=CC=C3)[Ag]43C4=C(C=CC(=C41)S2)N1C=CC2=C1/C3=C\C=C/2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3/C=C\C6=C3C(=CC=C6)[Ag]54N1=C2.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Ag]45N3/C=N(/C)C1=C23 Chemical compound C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3N(=CS5)[Ag]43C4=C(C=CC2=C41)C1=C/C=C/C=C\13.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=N(C=CC=C3)[Ag]43C4=C(C=CC(=C41)S2)N1C=CC2=C1/C3=C\C=C/2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3/C=C\C6=C3C(=CC=C6)[Ag]54N1=C2.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Ag]45N3/C=N(/C)C1=C23 SOZMONMCPLPWME-UHFFFAOYSA-N 0.000 description 1
- PXSPYKJBHLWIGY-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3N(=CS5)[Au]43C4=C(C=CC2=C41)C1=C/C=C/C=C\13.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=N(C=CC=C3)[Au]43C4=C(C=CC(=C41)S2)N1C=CC2=C1/C3=C\C=C/2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3/C=C\C6=C3C(=CC=C6)[Au]54N1=C2.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Au]45N3/C=N(/C)C1=C23 Chemical compound C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3N(=CS5)[Au]43C4=C(C=CC2=C41)C1=C/C=C/C=C\13.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=N(C=CC=C3)[Au]43C4=C(C=CC(=C41)S2)N1C=CC2=C1/C3=C\C=C/2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3/C=C\C6=C3C(=CC=C6)[Au]54N1=C2.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Au]45N3/C=N(/C)C1=C23 PXSPYKJBHLWIGY-UHFFFAOYSA-N 0.000 description 1
- DDAQCAYJAGADGF-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3N(=CS5)[Cu]43C4=C(C=CC2=C41)C1=C/C=C/C=C\13.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=N(C=CC=C3)[Cu]43C4=C(C=CC(=C41)S2)N1C=CC2=C1/C3=C\C=C/2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3/C=C\C6=C3C(=CC=C6)[Cu]54N1=C2.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Cu]45N3/C=N(/C)C1=C23 Chemical compound C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=CSC5=C3N(=CS5)[Cu]43C4=C(C=CC2=C41)C1=C/C=C/C=C\13.C1=CC2=C(C=C1)N1C3=C4C(=CC=C3)C3=N(C=CC=C3)[Cu]43C4=C(C=CC(=C41)S2)N1C=CC2=C1/C3=C\C=C/2.C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3/C=C\C6=C3C(=CC=C6)[Cu]54N1=C2.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Cu]45N3/C=N(/C)C1=C23 DDAQCAYJAGADGF-UHFFFAOYSA-N 0.000 description 1
- MIOGDQOXNJIDIY-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Mn]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Mn]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Mn]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Mn]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Mn]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Mn]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Mn]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Mn]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 MIOGDQOXNJIDIY-UHFFFAOYSA-Q 0.000 description 1
- XRWMHAZDAJKHSJ-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Ni]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Ni]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Ni]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Ni]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Ni]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Ni]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Ni]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Ni]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 XRWMHAZDAJKHSJ-UHFFFAOYSA-Q 0.000 description 1
- ALQLEIPAYUQGOJ-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Pd]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Pd]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Pd]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Pd]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Pd]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Pd]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Pd]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Pd]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 ALQLEIPAYUQGOJ-UHFFFAOYSA-Q 0.000 description 1
- FFZLGYRLPYUKBQ-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Pt]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Pt]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Pt]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Pt]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Pt]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Pt]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Pt]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Pt]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 FFZLGYRLPYUKBQ-UHFFFAOYSA-Q 0.000 description 1
- CFTFFESXRDUSHQ-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Zn]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Mn]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Mn]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Mn]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Zn]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=C\3[Mn]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Mn]23C2=C(C=CC5=C2/C6=C\O5)C2=CC=CC=N23)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Mn]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 CFTFFESXRDUSHQ-UHFFFAOYSA-Q 0.000 description 1
- OPFSAHVMABJTHH-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=C(C=CC=C3)[Ag]54N1=C2.C1=CC=C(/C2=[SH]/[Ag]34C5=C(C=CC6=C5N(C5=C(/C=C\C=C/5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4C4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Ag]432)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Ag]45N4/C=N(/C)C1=C24)O3 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=C(C=CC=C3)[Ag]54N1=C2.C1=CC=C(/C2=[SH]/[Ag]34C5=C(C=CC6=C5N(C5=C(/C=C\C=C/5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4C4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Ag]432)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Ag]45N4/C=N(/C)C1=C24)O3 OPFSAHVMABJTHH-UHFFFAOYSA-O 0.000 description 1
- MEGDQVNUMZNOOQ-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=C(C=CC=C3)[Au]54N1=C2.C1=CC=C(/C2=[SH]/[Au]34C5=C(C=CC6=C5N(C5=C(/C=C\C=C/5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4C4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Au]432)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Au]45N4/C=N(/C)C1=C24)O3 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=C(C=CC=C3)[Au]54N1=C2.C1=CC=C(/C2=[SH]/[Au]34C5=C(C=CC6=C5N(C5=C(/C=C\C=C/5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4C4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Au]432)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Au]45N4/C=N(/C)C1=C24)O3 MEGDQVNUMZNOOQ-UHFFFAOYSA-O 0.000 description 1
- SIDYNKRZPSLUJS-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=C(C=CC=C3)[Cu]54N1=C2.C1=CC=C(/C2=[SH]/[Cu]34C5=C(C=CC6=C5N(C5=C(/C=C\C=C/5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4C4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Cu]432)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Cu]45N4/C=N(/C)C1=C24)O3 Chemical compound C1=CC2=C(C=C1)N1C3=C4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C6=C(C=C3)OC=C6C3=C(C=CC=C3)[Cu]54N1=C2.C1=CC=C(/C2=[SH]/[Cu]34C5=C(C=CC6=C5N(C5=C(/C=C\C=C/5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/C4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4C4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Cu]432)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Cu]45N4/C=N(/C)C1=C24)O3 SIDYNKRZPSLUJS-UHFFFAOYSA-O 0.000 description 1
- QLGUNPSDRGWFGU-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=CC=CC4=C3C3(C5=CC=CC2=C51)C1=C2C(=CC=C1C1CCCC13)C1=C(C=CC=C1)N42.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC4=C(C=C1N23)C1=C(C=CC=C1)[U]4)C1CCCC61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC4=C(C=C1N23)[U]C1=C4C=CC=C1)C1CCCC61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC=C4[U]C5=C(C=CC=C5)C4=C1N23)C1CCCC61.CC.CC.CC.CC Chemical compound C1=CC2=C(C=C1)N1C3=CC=CC4=C3C3(C5=CC=CC2=C51)C1=C2C(=CC=C1C1CCCC13)C1=C(C=CC=C1)N42.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC4=C(C=C1N23)C1=C(C=CC=C1)[U]4)C1CCCC61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC4=C(C=C1N23)[U]C1=C4C=CC=C1)C1CCCC61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=CC=C6C(=C51)C4(C1=CC=C4[U]C5=C(C=CC=C5)C4=C1N23)C1CCCC61.CC.CC.CC.CC QLGUNPSDRGWFGU-UHFFFAOYSA-N 0.000 description 1
- TVDUWLIBPHNXDB-XYMTTYAISA-N C1=CC2=C(C=C1)N1C3=CC=CC4=N3[Au]3(C5=C(C=CC=C5)C5=C3C1=C2C=C5)/C1=C/C=C/C=C\41.CN1C2=C(C=CC=C2)C2=C1[Au]13C4=CC=CN4C4=C1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/N3=C/C5=COC6=C5C(=CO6)[Au]43C3/C=N(/C)C1=C23 Chemical compound C1=CC2=C(C=C1)N1C3=CC=CC4=N3[Au]3(C5=C(C=CC=C5)C5=C3C1=C2C=C5)/C1=C/C=C/C=C\41.CN1C2=C(C=CC=C2)C2=C1[Au]13C4=CC=CN4C4=C1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/N3=C/C5=COC6=C5C(=CO6)[Au]43C3/C=N(/C)C1=C23 TVDUWLIBPHNXDB-XYMTTYAISA-N 0.000 description 1
- RFTMFHHWVABGDD-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Co]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Co]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Co]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Co]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Co]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Co]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Co]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 RFTMFHHWVABGDD-UHFFFAOYSA-N 0.000 description 1
- BNRRXNNNKMKGJW-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Cu]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Cu]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Cu]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Cu]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Cu]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 BNRRXNNNKMKGJW-UHFFFAOYSA-N 0.000 description 1
- IRWNIJDOHOOVBB-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Ir]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Ir]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Ir]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Ir]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Ir]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Ir]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Ir]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 IRWNIJDOHOOVBB-UHFFFAOYSA-N 0.000 description 1
- WBCRPIZHCKEBPZ-UHFFFAOYSA-N C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Rh]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Rh]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Rh]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 Chemical compound C1=CC2=C(C=C1)N1C3=N(C=CC=C3)[Rh]3(C4=C5NC6=C(C=CC=C6)N5C5=C4C(=CS5)C4=N3C=CC=C4)N1=C2.C1=CC=C(N2C3=CC=CC4=C3[Rh]3(N5=CC=CC=C45)N4=C(C=CC5=C4C=CC=C5)C4=CC=CC5=C4N3=C2S5)C=C1.CN1C=C2C3=C1N(C)=CN3[Rh]13C4=C5C(=CC6=C4C(=CO6)C4=N1C=CC=C4)N(C)C1=C(C=CC=C1)N5C1=CC=CC2=N13.CN1C=C2C3=CC=CC=N3[Rh]34C5=C(C=CC=C5N5C6=C(C=CC=C6)C6=CC1=C2N3=C65)N1C=CC2=C1N4=CC=C2 WBCRPIZHCKEBPZ-UHFFFAOYSA-N 0.000 description 1
- LWLUPRGJAMTXFL-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Co]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Co]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Co]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Co]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Co]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Co]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Co]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Co]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 LWLUPRGJAMTXFL-UHFFFAOYSA-O 0.000 description 1
- NCELDWMXWCJJMX-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Cu]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Cu]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Cu]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Cu]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Cu]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Cu]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Cu]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Cu]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 NCELDWMXWCJJMX-UHFFFAOYSA-O 0.000 description 1
- RJVQLOSOKVUSEN-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Ir]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Ir]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Ir]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Ir]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Ir]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Ir]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Ir]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Ir]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 RJVQLOSOKVUSEN-UHFFFAOYSA-O 0.000 description 1
- DOEGIZVYQCUDRB-UHFFFAOYSA-O C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Rh]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Rh]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Rh]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Rh]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=C(C=CC=C8)[Rh]4(N1=C2)/N7=C\35)S6.C1=CC=C(/C2=[SiH]/[Rh]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=C\C=C5\C=CC=C2\C5=N\34)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Rh]2(C2=CC=CC=C27)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Rh]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1 DOEGIZVYQCUDRB-UHFFFAOYSA-O 0.000 description 1
- AFUJAFVSZUROQM-UHFFFAOYSA-P C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Co]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Co]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Co]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Co]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Co]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Co]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 AFUJAFVSZUROQM-UHFFFAOYSA-P 0.000 description 1
- WNHBNNUQKVYOFQ-UHFFFAOYSA-P C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Cu]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Cu]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Cu]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Cu]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Cu]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Cu]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 WNHBNNUQKVYOFQ-UHFFFAOYSA-P 0.000 description 1
- LJZSSOOKMSYVRF-UHFFFAOYSA-P C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Ir]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Ir]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Ir]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Ir]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Ir]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Ir]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 LJZSSOOKMSYVRF-UHFFFAOYSA-P 0.000 description 1
- CRRFNYOEOORPII-UHFFFAOYSA-P C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Rh]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Rh]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Rh]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 Chemical compound C1=CC2=C(C=C1)N1C3=N4C(=CC=C3)N3C5=C(C=CC=C5)N5C6=C7C8=C(CCN8C8=N(C=CC=C8)[Cu]4(/C7=C\35)N1=C2)S6.C1=CC=C(/C2=[SH]/[Rh]34C5=C(C=CC=C5N(C5=CC=CC=C5)C5=C\C=C6\C=CC=C2\C6=N\53)/C2=C/C=C\C3=C2N4=CC=C3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)N5C6=CC=CC7=C6[Rh]2(N2=CC=CC=C72)N3=C54)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Rh]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2 CRRFNYOEOORPII-UHFFFAOYSA-P 0.000 description 1
- FOECNGBKLRXKCM-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Co]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Co]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Co]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Co]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Co]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Co]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Co]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Co]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 FOECNGBKLRXKCM-UHFFFAOYSA-Q 0.000 description 1
- YJTGLCXBEIHYLF-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Cu]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Cu]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Cu]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Cu]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Cu]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Cu]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Cu]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Cu]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 YJTGLCXBEIHYLF-UHFFFAOYSA-Q 0.000 description 1
- IDNWYBKWLSNBDX-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Ir]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Ir]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Ir]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Ir]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Ir]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Ir]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Ir]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Ir]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 IDNWYBKWLSNBDX-UHFFFAOYSA-Q 0.000 description 1
- CUFJPAYKTWLCAQ-UHFFFAOYSA-Q C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Rh]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Rh]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Rh]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Rh]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 Chemical compound C1=CC2=C(C=C1)N1C3=N4C5=C(C=C3)C3=C(C=CC=C3)N5C3=C5C(=CC=C3)N3C=CC6=C3N(=CC=C6)[Rh]54N1=C2.C1=CC=C([PH]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)O/C4=N\3[Rh]23C2=C(C=CC5=C2C4=CC=C5)C2=CC=CC=N23)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C5=C3[Rh]23N2=CC=CC=C2C2=N3C3=C(C=C2)O/C=C\36)S4)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5C6=C(C=C3C=C4)C3=C(C=CC=C3)N6C3=CC=CC4=N3[Rh]52N2=CC=CC3=C2/C4=C\C=C/3)C=C1 CUFJPAYKTWLCAQ-UHFFFAOYSA-Q 0.000 description 1
- QHVGSOIJFXHLNS-UHFFFAOYSA-P C1=CC2=C3/C(=C\C=C/2)C2=C4C(=CC=C2)N2C5=C(C=CC=C5)OC5=C2/C2=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Ag]42N3=C1.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ag]43C4=CC=CN4C4=COC5=C4/C3=C/2O5)C=C1.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Ag]23C4=C(C=CC=C4N4C(C)=C(C)C5=C4C2=C1O5)C1=CC=CC2=C1C3C=N2C.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Ag]312 Chemical compound C1=CC2=C3/C(=C\C=C/2)C2=C4C(=CC=C2)N2C5=C(C=CC=C5)OC5=C2/C2=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Ag]42N3=C1.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ag]43C4=CC=CN4C4=COC5=C4/C3=C/2O5)C=C1.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Ag]23C4=C(C=CC=C4N4C(C)=C(C)C5=C4C2=C1O5)C1=CC=CC2=C1C3C=N2C.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Ag]312 QHVGSOIJFXHLNS-UHFFFAOYSA-P 0.000 description 1
- KYPKOVUAPKABJT-UHFFFAOYSA-P C1=CC2=C3/C(=C\C=C/2)C2=C4C(=CC=C2)N2C5=C(C=CC=C5)OC5=C2/C2=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Au]42N3=C1.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Au]43C4=CC=CN4C4=COC5=C4/C3=C/2O5)C=C1.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Au]23C4=C(C=CC=C4N4C(C)=C(C)C5=C4C2=C1O5)C1=CC=CC2=C1C3C=N2C.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Au]312 Chemical compound C1=CC2=C3/C(=C\C=C/2)C2=C4C(=CC=C2)N2C5=C(C=CC=C5)OC5=C2/C2=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Au]42N3=C1.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Au]43C4=CC=CN4C4=COC5=C4/C3=C/2O5)C=C1.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Au]23C4=C(C=CC=C4N4C(C)=C(C)C5=C4C2=C1O5)C1=CC=CC2=C1C3C=N2C.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Au]312 KYPKOVUAPKABJT-UHFFFAOYSA-P 0.000 description 1
- QNCJOGMRULJUKX-UHFFFAOYSA-P C1=CC2=C3/C(=C\C=C/2)C2=C4C(=CC=C2)N2C5=C(C=CC=C5)OC5=C2/C2=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Cu]42N3=C1.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Cu]43C4=CC=CN4C4=COC5=C4/C3=C/2O5)C=C1.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Cu]23C4=C(C=CC=C4N4C(C)=C(C)C5=C4C2=C1O5)C1=CC=CC2=C1C3C=N2C.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Cu]312 Chemical compound C1=CC2=C3/C(=C\C=C/2)C2=C4C(=CC=C2)N2C5=C(C=CC=C5)OC5=C2/C2=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Cu]42N3=C1.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Cu]43C4=CC=CN4C4=COC5=C4/C3=C/2O5)C=C1.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Cu]23C4=C(C=CC=C4N4C(C)=C(C)C5=C4C2=C1O5)C1=CC=CC2=C1C3C=N2C.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Cu]312 QNCJOGMRULJUKX-UHFFFAOYSA-P 0.000 description 1
- VTNXPMCHGBNPCD-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Co]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Co]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Co]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Co]423 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Co]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Co]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Co]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Co]423 VTNXPMCHGBNPCD-UHFFFAOYSA-O 0.000 description 1
- KFNJICBBECXPSA-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Cu]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Cu]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Cu]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Cu]423 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Cu]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Cu]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Cu]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Cu]423 KFNJICBBECXPSA-UHFFFAOYSA-O 0.000 description 1
- SYHVUIGFTBDIIB-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Ir]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ir]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Ir]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Ir]423 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Ir]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ir]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Ir]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Ir]423 SYHVUIGFTBDIIB-UHFFFAOYSA-O 0.000 description 1
- QHCLTXFMICGBFJ-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Ni]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ni]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Ni]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Ni]342 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Ni]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Ni]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Ni]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Ni]342 QHCLTXFMICGBFJ-UHFFFAOYSA-O 0.000 description 1
- FDYQRTZBVONKOE-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Pd]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pd]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Pd]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Pd]342 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Pd]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pd]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Pd]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Pd]342 FDYQRTZBVONKOE-UHFFFAOYSA-O 0.000 description 1
- WYXMSZBDELFHMD-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Pt]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pt]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Pt]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Pt]342 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Pt]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Pt]43C4=C2OC2=C4C(=CO2)N2C=CC=N23)C=C1.CN1C=CN2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Pt]312.CN1C=N2C3=C(C=CC=C31)C1=C3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Pt]342 WYXMSZBDELFHMD-UHFFFAOYSA-O 0.000 description 1
- MUVNUKYVHFIKSY-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Rh]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Rh]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Rh]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Rh]423 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Rh]41N3=CC=C2.C1=CC=C(N2C3=C4C(=CC=C3)O[PH](C3=CC=CC=C3)(C3=CC=CC=C3)[Rh]43N4=CC=CN4C4=COC5=C4N3=C2O5)C=C1.CN1C=CN2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Rh]321.CN1C=N2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=C4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Rh]423 MUVNUKYVHFIKSY-UHFFFAOYSA-O 0.000 description 1
- ODIGLECBRMTDHX-AUFXHVKZSA-N C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Ag]41C3=CC=C2.C1=CC=C(N2C3=CC=CC4=C3[Ag]3(C5=CO/C6=C/C=C\C4=C56)C4=CC=CC5=C4N(/C=C\5)C4=N3C2=CC=C4)C=C1.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)CN3=C/C5=C/OC6=C5C(=CO6)[Ag]43C3/C=N(/C)C1=C23 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Ag]41C3=CC=C2.C1=CC=C(N2C3=CC=CC4=C3[Ag]3(C5=CO/C6=C/C=C\C4=C56)C4=CC=CC5=C4N(/C=C\5)C4=N3C2=CC=C4)C=C1.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)CN3=C/C5=C/OC6=C5C(=CO6)[Ag]43C3/C=N(/C)C1=C23 ODIGLECBRMTDHX-AUFXHVKZSA-N 0.000 description 1
- AVQUHBCFPVCGKU-AUFXHVKZSA-N C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Cu]41C3=CC=C2.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(C5=CO/C6=C/C=C\C4=C56)C4=CC=CC5=C4N(/C=C\5)C4=N3C2=CC=C4)C=C1.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)CN3=C/C5=C/OC6=C5C(=CO6)[Cu]43C3/C=N(/C)C1=C23 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Cu]41C3=CC=C2.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(C5=CO/C6=C/C=C\C4=C56)C4=CC=CC5=C4N(/C=C\5)C4=N3C2=CC=C4)C=C1.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)CN3=C/C5=C/OC6=C5C(=CO6)[Cu]43C3/C=N(/C)C1=C23 AVQUHBCFPVCGKU-AUFXHVKZSA-N 0.000 description 1
- BXKRPLWTQBYPFB-UHFFFAOYSA-N C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1\N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Au]41C3=CC=C2.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=COC6=CC=CC4=C65)C4=CC=CC5=C4N(/C=C\5)C4=N3C2=CC=C4)C=C1.C1=CC=C(N2CC3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Au]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1 Chemical compound C1=CC2=C3C(=C1)C1=C4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1\N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Au]41C3=CC=C2.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=COC6=CC=CC4=C65)C4=CC=CC5=C4N(/C=C\5)C4=N3C2=CC=C4)C=C1.C1=CC=C(N2CC3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Au]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1 BXKRPLWTQBYPFB-UHFFFAOYSA-N 0.000 description 1
- QNDYQAFCVPBFMV-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Co]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Co]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Co]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Co]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Co]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Co]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Co]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Co]231 QNDYQAFCVPBFMV-UHFFFAOYSA-O 0.000 description 1
- KDCWGBLUBJSPIE-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Cu]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Cu]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Cu]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Cu]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Cu]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Cu]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Cu]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Cu]231 KDCWGBLUBJSPIE-UHFFFAOYSA-O 0.000 description 1
- MPJRJMSDEUILEM-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Ir]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Ir]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Ir]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Ir]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Ir]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Ir]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Ir]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Ir]231 MPJRJMSDEUILEM-UHFFFAOYSA-O 0.000 description 1
- KGTKUYYMMJUDPS-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Rh]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Rh]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Rh]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Rh]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1/N1=C(\C=C/5)N5C6=C(C=CC=C6)C6=C5N(=CC=C6)[Rh]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Rh]34N3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=N3/C4=C(\C=C/1)N(C)C1=C(C=CC=C1)N4/C1=N4/C5=C(C=CC=C5N1C)C1=CC=CC=N1[Rh]234.CN1C=CC2=C1N1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4N(=CC=C5)[Rh]231 KGTKUYYMMJUDPS-UHFFFAOYSA-O 0.000 description 1
- QYCZXOCVVAJHIB-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Mn]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Mn]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=C1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Mn]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Mn]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Mn]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=C1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Mn]231 QYCZXOCVVAJHIB-UHFFFAOYSA-O 0.000 description 1
- SIPMIBUNBHDMHK-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Ni]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Ni]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=N1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Ni]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Ni]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Ni]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=N1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Ni]231 SIPMIBUNBHDMHK-UHFFFAOYSA-O 0.000 description 1
- XRCPNYLVGYDLRW-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Pd]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Pd]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=C1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Pd]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Pd]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Pd]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=C1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Pd]231 XRCPNYLVGYDLRW-UHFFFAOYSA-O 0.000 description 1
- BOUHKMYHIIOSRA-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Pt]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Pt]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=N1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Pt]231 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Pt]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Pt]34C3=CC=CN3C3=COC5=C3N4=C2O5)C=C1.CN1C=CC2=N1N1C=CC3=C1N1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Pt]231 BOUHKMYHIIOSRA-UHFFFAOYSA-O 0.000 description 1
- BGOPJOHSHQZDRN-UHFFFAOYSA-O C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Zn]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Zn]34C3=CC=CN3C3=COC5=C3C4=C2O5)C=C1.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Zn]123 Chemical compound C1=CC2=C3C(=C1)C1=N4C(=CC=C1)N1C5=C(C=CC=C5)OC5=C1N1=C(C=C5)N5C6=C(C=CC=C6)C6=C5C(=CC=C6)[Zn]41C3=CC=C2.C1=CC=C(N2C[PH]3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Zn]34C3=CC=CN3C3=COC5=C3C4=C2O5)C=C1.CN1C=CC2=N1N1C=CC3=C1C1=C(/C=C\3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Zn]123 BGOPJOHSHQZDRN-UHFFFAOYSA-O 0.000 description 1
- VYOXVNLXJOZKLM-UHFFFAOYSA-N C1=CC2=C3C(=C1)CC1CCCC1C31C3=C(C=CC=C3C2)C2CCCC21.CC.CC.CC.CC Chemical compound C1=CC2=C3C(=C1)CC1CCCC1C31C3=C(C=CC=C3C2)C2CCCC21.CC.CC.CC.CC VYOXVNLXJOZKLM-UHFFFAOYSA-N 0.000 description 1
- YADLSWYGXVRQMQ-UHFFFAOYSA-N C1=CC2=C3C(=C1)CC1CCCC1C31C3=C(CCC=C3C2)C2CCCC21.CC.CC.CC.CC Chemical compound C1=CC2=C3C(=C1)CC1CCCC1C31C3=C(CCC=C3C2)C2CCCC21.CC.CC.CC.CC YADLSWYGXVRQMQ-UHFFFAOYSA-N 0.000 description 1
- BESZOUBPISSDCH-UHFFFAOYSA-N C1=CC2=C3C(=C1)N1C=CC4=C1/C1=C(\O4)C4=CSC=C4[Ag]31N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Ag]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Ag]231.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5/N(=C\O6)[Ag]43N3C=N(C)C1=C23 Chemical compound C1=CC2=C3C(=C1)N1C=CC4=C1/C1=C(\O4)C4=CSC=C4[Ag]31N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Ag]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Ag]231.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5/N(=C\O6)[Ag]43N3C=N(C)C1=C23 BESZOUBPISSDCH-UHFFFAOYSA-N 0.000 description 1
- ZSVUWEWDUYWGST-UHFFFAOYSA-N C1=CC2=C3C(=C1)N1C=CC4=C1/C1=C(\O4)C4=CSC=C4[Au]31N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Au]231.CN1=CN2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5/N(=C\O6)[Au]43N3C=N(C)C1=C23 Chemical compound C1=CC2=C3C(=C1)N1C=CC4=C1/C1=C(\O4)C4=CSC=C4[Au]31N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Au]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Au]231.CN1=CN2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5/N(=C\O6)[Au]43N3C=N(C)C1=C23 ZSVUWEWDUYWGST-UHFFFAOYSA-N 0.000 description 1
- QQYMYWJVFBOKHW-UHFFFAOYSA-N C1=CC2=C3C(=C1)N1C=CC4=C1/C1=C(\O4)C4=CSC=C4[Cu]31N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Cu]231.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5/N(=C\O6)[Cu]43N3C=N(C)C1=C23 Chemical compound C1=CC2=C3C(=C1)N1C=CC4=C1/C1=C(\O4)C4=CSC=C4[Cu]31N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Cu]231.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5/N(=C\O6)[Cu]43N3C=N(C)C1=C23 QQYMYWJVFBOKHW-UHFFFAOYSA-N 0.000 description 1
- MQBUETAFOXOALD-UHFFFAOYSA-O C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Ni]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Ni]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Ni]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Ni]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Ni]43N3/C=N(/C)C1=C23 Chemical compound C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Ni]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Ni]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Ni]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Ni]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Ni]43N3/C=N(/C)C1=C23 MQBUETAFOXOALD-UHFFFAOYSA-O 0.000 description 1
- UECNXHYCKYGEGM-UHFFFAOYSA-O C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Pd]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Pd]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Pd]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Pd]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Pd]43N3/C=N(/C)C1=C23 Chemical compound C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Pd]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Pd]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Pd]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Pd]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Pd]43N3/C=N(/C)C1=C23 UECNXHYCKYGEGM-UHFFFAOYSA-O 0.000 description 1
- PQLZWVISZZRGRI-UHFFFAOYSA-O C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Pt]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Pt]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Pt]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Pt]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Pt]43N3/C=N(/C)C1=C23 Chemical compound C1=CC2=C3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Pt]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Pt]3(C5=C(C=CC=C52)N2/C=C\C5=C2N3=CC=C5)/N2=C/OC3=CC=CC4=C32)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Pt]312.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Pt]23C4=C(C=CC=C4N4C5=C(OC1=C52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C4C(=CC=C3)N(C3=CC=CC=C3)C/C3=C/C5=COC6=C5N(=CO6)[Pt]43N3/C=N(/C)C1=C23 PQLZWVISZZRGRI-UHFFFAOYSA-O 0.000 description 1
- USFHIFIIDQOPQT-UHFFFAOYSA-N C1=CC2=C3C(=C1)[Ag]14C5=C(C=CC=C5)C5=CC=CC(=C51)N1C5=C(C=CC=C5)SC5=C1N4=C(C=C5)N3C=C2.CN1=CC2C3=C1/C=C\C=C3\C1=C3\C4=C(/C=C\1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Ag]324.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Ag]45C3=CN(C)C1=C23 Chemical compound C1=CC2=C3C(=C1)[Ag]14C5=C(C=CC=C5)C5=CC=CC(=C51)N1C5=C(C=CC=C5)SC5=C1N4=C(C=C5)N3C=C2.CN1=CC2C3=C1/C=C\C=C3\C1=C3\C4=C(/C=C\1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Ag]324.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Ag]45C3=CN(C)C1=C23 USFHIFIIDQOPQT-UHFFFAOYSA-N 0.000 description 1
- TZUSKOFFFMNHMF-UHFFFAOYSA-N C1=CC2=C3C(=C1)[Au]14C5=C(C=CC=C5)C5=CC=CC(=C51)N1C5=C(C=CC=C5)SC5=C1N4=C(C=C5)N3C=C2.CN1=CC2C3=C1/C=C\C=C3\C1=C3\C4=C(/C=C\1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Au]324.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Au]45C3=CN(C)C1=C23 Chemical compound C1=CC2=C3C(=C1)[Au]14C5=C(C=CC=C5)C5=CC=CC(=C51)N1C5=C(C=CC=C5)SC5=C1N4=C(C=C5)N3C=C2.CN1=CC2C3=C1/C=C\C=C3\C1=C3\C4=C(/C=C\1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Au]324.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Au]45C3=CN(C)C1=C23 TZUSKOFFFMNHMF-UHFFFAOYSA-N 0.000 description 1
- ZNNSQAFWMUFCQO-UHFFFAOYSA-N C1=CC2=C3C(=C1)[Cu]14C5=C(C=CC=C5)C5=CC=CC(=C51)N1C5=C(C=CC=C5)SC5=C1N4=C(C=C5)N3C=C2.CN1=CC2C3=C1/C=C\C=C3\C1=C3\C4=C(/C=C\1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Cu]324.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Cu]45C3=CN(C)C1=C23 Chemical compound C1=CC2=C3C(=C1)[Cu]14C5=C(C=CC=C5)C5=CC=CC(=C51)N1C5=C(C=CC=C5)SC5=C1N4=C(C=C5)N3C=C2.CN1=CC2C3=C1/C=C\C=C3\C1=C3\C4=C(/C=C\1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Cu]324.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C(=CC=C3)C3=CC=CC6=C3C(=CS6)[Cu]45C3=CN(C)C1=C23 ZNNSQAFWMUFCQO-UHFFFAOYSA-N 0.000 description 1
- ISZBRCFHNXPYGY-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Mn]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Mn]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Mn]342.CN1C=C2C3=C1/N(C)=C\N3[Mn]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Mn]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Mn]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Mn]342.CN1C=C2C3=C1/N(C)=C\N3[Mn]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 ISZBRCFHNXPYGY-UHFFFAOYSA-N 0.000 description 1
- BXKRAZLTUKBSNY-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Ni]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Ni]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Ni]342.CN1C=C2C3=C1/N(C)=C\N3[Ni]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Ni]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Ni]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Ni]342.CN1C=C2C3=C1/N(C)=C\N3[Ni]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 BXKRAZLTUKBSNY-UHFFFAOYSA-N 0.000 description 1
- BXWJYPCJRILCSI-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Pd]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Pd]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Pd]342.CN1C=C2C3=C1/N(C)=C\N3[Pd]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Pd]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Pd]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Pd]342.CN1C=C2C3=C1/N(C)=C\N3[Pd]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 BXWJYPCJRILCSI-UHFFFAOYSA-N 0.000 description 1
- VSQALJMCXZVDFQ-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Pt]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Pt]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Pt]342.CN1C=C2C3=C1/N(C)=C\N3[Pt]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Pt]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Pt]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Pt]342.CN1C=C2C3=C1/N(C)=C\N3[Pt]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 VSQALJMCXZVDFQ-UHFFFAOYSA-N 0.000 description 1
- VLHVEMNTIHPGMF-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Zn]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Zn]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Zn]342.CN1C=C2C3=C1/N(C)=C\N3[Zn]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=C5C(=CC=C2)C2=N(C=CC=C2)[Zn]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Zn]342.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Zn]342.CN1C=C2C3=C1/N(C)=C\N3[Zn]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/C3=C2\C=C/4 VLHVEMNTIHPGMF-UHFFFAOYSA-N 0.000 description 1
- APIOHLVLLFWQJB-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Co]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Co]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Co]423.CN1C=C2C3=C1/N(C)=C\N3[Co]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Co]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Co]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Co]423.CN1C=C2C3=C1/N(C)=C\N3[Co]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 APIOHLVLLFWQJB-UHFFFAOYSA-N 0.000 description 1
- WFTVUGMMZVBVFJ-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Cu]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Cu]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Cu]423.CN1C=C2C3=C1/N(C)=C\N3[Cu]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Cu]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Cu]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Cu]423.CN1C=C2C3=C1/N(C)=C\N3[Cu]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 WFTVUGMMZVBVFJ-UHFFFAOYSA-N 0.000 description 1
- KQFRKQMOLFMQEU-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Ir]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Ir]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Ir]423.CN1C=C2C3=C1/N(C)=C\N3[Ir]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Ir]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Ir]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Ir]423.CN1C=C2C3=C1/N(C)=C\N3[Ir]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 KQFRKQMOLFMQEU-UHFFFAOYSA-N 0.000 description 1
- DJNGGPCNNBLZSR-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Rh]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Rh]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Rh]423.CN1C=C2C3=C1/N(C)=C\N3[Rh]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=C4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=N(C=CC=C2)[Rh]45N3=C1.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Rh]324.CN1=CN2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Rh]423.CN1C=C2C3=C1/N(C)=C\N3[Rh]13C4=C(C=CC=C4/C4=C/C=C\C5=C4N1=CS5)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 DJNGGPCNNBLZSR-UHFFFAOYSA-N 0.000 description 1
- JSAPTRGFIQIFCX-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Co]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Co]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Co]234.CN1C=C2C3=C1/N(C)=C\N3[Co]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Co]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Co]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Co]234.CN1C=C2C3=C1/N(C)=C\N3[Co]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 JSAPTRGFIQIFCX-UHFFFAOYSA-N 0.000 description 1
- VOMYZRATGVWFPV-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Cu]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Cu]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Cu]234.CN1C=C2C3=C1/N(C)=C\N3[Cu]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Cu]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Cu]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Cu]234.CN1C=C2C3=C1/N(C)=C\N3[Cu]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 VOMYZRATGVWFPV-UHFFFAOYSA-N 0.000 description 1
- CNDHDQKHLOBVAH-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Ir]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Ir]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Ir]234.CN1C=C2C3=C1/N(C)=C\N3[Ir]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Ir]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Ir]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Ir]234.CN1C=C2C3=C1/N(C)=C\N3[Ir]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 CNDHDQKHLOBVAH-UHFFFAOYSA-N 0.000 description 1
- QXMQGQXNSQHUJP-UHFFFAOYSA-N C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Rh]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Rh]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Rh]234.CN1C=C2C3=C1/N(C)=C\N3[Rh]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 Chemical compound C1=CC2=C3N(C=C2)C2=N4C5=C(C=C2)SC2=C(C=CC=C2)N5C2=N5C(=CC=C2)C2=C(C=CC=C2)[Rh]45N3=C1.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4C(=CC=C1)/C1=C/SC5=C1N(=CS5)[Rh]234.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1/N(=C\C=C/5)[Rh]234.CN1C=C2C3=C1/N(C)=C\N3[Rh]13C4=CSC5=C4/C(=C\C=C/5)C4=CC=CC(=N41)N1C4=C(C=CC=C4)N(C)C4=C1/N3=C2\C=C/4 QXMQGQXNSQHUJP-UHFFFAOYSA-N 0.000 description 1
- PUNCXCMJLGFBIZ-UHFFFAOYSA-O C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Co]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Co]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Co]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Co]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Co]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Co]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Co]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Co]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Co]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Co]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 PUNCXCMJLGFBIZ-UHFFFAOYSA-O 0.000 description 1
- FANDKCWOCKEWFZ-UHFFFAOYSA-O C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Cu]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Cu]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Cu]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Cu]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Cu]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Cu]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Cu]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Cu]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Cu]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 FANDKCWOCKEWFZ-UHFFFAOYSA-O 0.000 description 1
- XEEIQDQHXZXZBD-UHFFFAOYSA-O C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Ir]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Ir]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Ir]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Ir]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Ir]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Ir]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Ir]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Ir]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Ir]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Ir]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 XEEIQDQHXZXZBD-UHFFFAOYSA-O 0.000 description 1
- BSVVZJFVYGXVPU-UHFFFAOYSA-O C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Rh]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Rh]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Rh]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Rh]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Rh]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC2=N3C(=C1)N1C=CC4=C1C1=C(O4)C4=CSC=N4[Rh]13N1=CC=CN21.C1=CC=C(N2C3=CC=CC4=C3[Rh]3(N5=CC=CC6=C5N4/C=C\6)N4=C(C=CC=C24)C2=C4C(=CC=C2)O/C=N\43)C=C1.C1=CC=N2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C(\C=C/4)C4=N(C=CC=C4)[Rh]123.CCN1O[PH](C2=CC=CC=C2)(C2=CC=CC=C2)[Rh]23C4=C(C=CC=C4N4C5=C(OC1=N52)C(C)C4C)/C1=C/C=C\C2=C1N3C=N2C.CN1C=C2C3=C1/N(C)=C\N3[Rh]13/C(=C\C4=COC5=C4N1=CO5)CN(C1=CC=CC=C1)C1=CC=CC2=N13 BSVVZJFVYGXVPU-UHFFFAOYSA-O 0.000 description 1
- PBMXWPFQMDDZMO-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Ag]34C5=CC=CC6=C5/C(=C\C=C/6)C5=C3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=C34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Ag]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)/C5=C/C6=C7C(=CO6)C6=N(C=CC=C6)[Ag]4(C7=C53)C3/C=N(/C)C1=C23.CN1C=C2C3=CC=CC=N3[Ag]34C5=CC=CC6=C5N(C=C6)C5=C3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 Chemical compound C1=CC=C(/C2=[SH]/[Ag]34C5=CC=CC6=C5/C(=C\C=C/6)C5=C3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=C34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Ag]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)/C5=C/C6=C7C(=CO6)C6=N(C=CC=C6)[Ag]4(C7=C53)C3/C=N(/C)C1=C23.CN1C=C2C3=CC=CC=N3[Ag]34C5=CC=CC6=C5N(C=C6)C5=C3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 PBMXWPFQMDDZMO-UHFFFAOYSA-O 0.000 description 1
- MGRLMJWGTJAEHU-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Ag]34C5=CC=CC6=C5C(=CC=C6)C5=C3C3=C(C=C5)CCC5=C(C=CC=C5)N3C3=C4C4=C(O/C=C/42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Ag]342)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Ag]45C4=CN(C)C1=C24)O3 Chemical compound C1=CC=C(/C2=[SH]/[Ag]34C5=CC=CC6=C5C(=CC=C6)C5=C3C3=C(C=C5)CCC5=C(C=CC=C5)N3C3=C4C4=C(O/C=C/42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Ag]342)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Ag]45C4=CN(C)C1=C24)O3 MGRLMJWGTJAEHU-UHFFFAOYSA-O 0.000 description 1
- MGWUFJLJGSRCPI-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Au]34C5=CC=CC6=C5/C(=C\C=C/6)C5=C3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=C34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Au]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)/C5=C/C6=C7C(=CO6)C6=N(C=CC=C6)[Au]4(C7=C53)C3/C=N(/C)C1=C23.CN1C=C2C3=CC=CC=N3[Au]34C5=CC=CC6=C5N(C=C6)C5=C3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 Chemical compound C1=CC=C(/C2=[SH]/[Au]34C5=CC=CC6=C5/C(=C\C=C/6)C5=C3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=C34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Au]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)/C5=C/C6=C7C(=CO6)C6=N(C=CC=C6)[Au]4(C7=C53)C3/C=N(/C)C1=C23.CN1C=C2C3=CC=CC=N3[Au]34C5=CC=CC6=C5N(C=C6)C5=C3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 MGWUFJLJGSRCPI-UHFFFAOYSA-O 0.000 description 1
- PBISSFGGEJMNTE-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Au]34C5=CC=CC6=C5C(=CC=C6)C5=C3C3=C(C=C5)CCC5=C(C=CC=C5)N3C3=C4C4=C(O/C=C/42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Au]342)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Au]45C4=CN(C)C1=C24)O3 Chemical compound C1=CC=C(/C2=[SH]/[Au]34C5=CC=CC6=C5C(=CC=C6)C5=C3C3=C(C=C5)CCC5=C(C=CC=C5)N3C3=C4C4=C(O/C=C/42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Au]342)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Au]45C4=CN(C)C1=C24)O3 PBISSFGGEJMNTE-UHFFFAOYSA-O 0.000 description 1
- XSAUWFOBIQNJDL-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Co]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Co]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Co]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Co]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Co]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Co]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Co]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Co]53N2=C1)O4 XSAUWFOBIQNJDL-UHFFFAOYSA-O 0.000 description 1
- COHPOSNUABBCST-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Co]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Co]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Co]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Co]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Co]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Co]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Co]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Co]53N2=C1)O4 COHPOSNUABBCST-UHFFFAOYSA-O 0.000 description 1
- ZLMLUZLBJIMHOD-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Cu]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Cu]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Cu]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Cu]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Cu]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Cu]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Cu]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Cu]53N2=C1)O4 ZLMLUZLBJIMHOD-UHFFFAOYSA-O 0.000 description 1
- CJOCRLKSAJHROD-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Cu]34C5=CC=CC6=C5/C(=C\C=C/6)C5=C3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=C34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Cu]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)/C5=C/C6=C7C(=CO6)C6=N(C=CC=C6)[Cu]4(C7=C53)C3/C=N(/C)C1=C23.CN1C=C2C3=CC=CC=N3[Cu]34C5=CC=CC6=C5N(C=C6)C5=C3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 Chemical compound C1=CC=C(/C2=[SH]/[Cu]34C5=CC=CC6=C5/C(=C\C=C/6)C5=C3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=C34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=C3[Cu]3(C5=C6C(=CC1=C52)/C=C\C=C/6[PH]3(C1=CC=CC=C1)C1=CC=CC=C1)N1C=N(C)C2=C1/C4=C\C=C/2.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)/C5=C/C6=C7C(=CO6)C6=N(C=CC=C6)[Cu]4(C7=C53)C3/C=N(/C)C1=C23.CN1C=C2C3=CC=CC=N3[Cu]34C5=CC=CC6=C5N(C=C6)C5=C3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 CJOCRLKSAJHROD-UHFFFAOYSA-O 0.000 description 1
- QQUUHHWZJQVYSZ-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Cu]34C5=CC=CC6=C5C(=CC=C6)C5=C3C3=C(C=C5)CCC5=C(C=CC=C5)N3C3=C4C4=C(O/C=C/42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Cu]342)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Cu]45C4=CN(C)C1=C24)O3 Chemical compound C1=CC=C(/C2=[SH]/[Cu]34C5=CC=CC6=C5C(=CC=C6)C5=C3C3=C(C=C5)CCC5=C(C=CC=C5)N3C3=C4C4=C(O/C=C/42)O3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(C=C4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5C(=CC=C6)[Cu]342)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC=C6C6=C(OC7=C6C=CC=C7)[Cu]45C4=CN(C)C1=C24)O3 QQUUHHWZJQVYSZ-UHFFFAOYSA-O 0.000 description 1
- HJCNNPFTSBWDFP-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Cu]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Cu]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Cu]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Cu]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Cu]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Cu]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Cu]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Cu]53N2=C1)O4 HJCNNPFTSBWDFP-UHFFFAOYSA-O 0.000 description 1
- ZTJIDURAXJWHPW-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Ir]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Ir]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Ir]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Ir]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Ir]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Ir]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Ir]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Ir]53N2=C1)O4 ZTJIDURAXJWHPW-UHFFFAOYSA-O 0.000 description 1
- BIVODFUGCPUUBB-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Ir]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Ir]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Ir]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Ir]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Ir]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Ir]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Ir]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Ir]53N2=C1)O4 BIVODFUGCPUUBB-UHFFFAOYSA-O 0.000 description 1
- CJBKDWJNBOPRLY-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Mn]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Mn]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Mn]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Mn]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Mn]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Mn]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Mn]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Mn]53N2=C1)O4 CJBKDWJNBOPRLY-UHFFFAOYSA-O 0.000 description 1
- HSCLSPIBRUBUIL-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Ni]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Ni]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Ni]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Ni]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Ni]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Ni]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Ni]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Ni]53N2=C1)O4 HSCLSPIBRUBUIL-UHFFFAOYSA-O 0.000 description 1
- GJWLMEJPLYKZBM-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Pd]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Pd]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Pd]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Pd]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Pd]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Pd]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Pd]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Pd]53N2=C1)O4 GJWLMEJPLYKZBM-UHFFFAOYSA-O 0.000 description 1
- PILMWCVXWPLOBO-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Pt]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Pt]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Pt]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Pt]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Pt]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Pt]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Pt]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Pt]53N2=C1)O4 PILMWCVXWPLOBO-UHFFFAOYSA-O 0.000 description 1
- YXPOZJCLOALFDG-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Rh]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Rh]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Rh]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Rh]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Rh]34C5=C(OC6=C5C2=CO6)N2C5=C(C=CC=C5)CCC5=C2N3=C(C=C5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Rh]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Rh]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Rh]53N2=C1)O4 YXPOZJCLOALFDG-UHFFFAOYSA-O 0.000 description 1
- XVAIYLUQLWMFTE-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Rh]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Rh]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Rh]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Rh]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Rh]34N5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=N3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N3=C(\C=C/4)N4C5=C(C=CC=C5)SC5=C4N4=C(C=C5)N5C=CC6=C5N(=CC=C6)[Rh]432)C=C1.CC1=CC(C)=N2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Rh]142)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Rh]53N2=C1)O4 XVAIYLUQLWMFTE-UHFFFAOYSA-O 0.000 description 1
- CBDSHYPZJZJXQD-UHFFFAOYSA-O C1=CC=C(/C2=[SH]/[Zn]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Zn]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Zn]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Zn]53N2=C1)O4 Chemical compound C1=CC=C(/C2=[SH]/[Zn]34C5=C(C=CC6=C5N(C5=C(C=CC=C5)CC6)C5=C3C3=C(OC=C32)O5)C2=CC=CC3=C2/N4=C\C=C/3)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3/N(=C\C=C/4)[Zn]23C2=C(C=CC4=C2NC2=C(C=CC=C2)S4)N2C=CC4=C2N3=CC=C4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=N(C=CC=C5CC6)[Zn]142)N3C.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=N(C=CC=C6)[Zn]53N2=C1)O4 CBDSHYPZJZJXQD-UHFFFAOYSA-O 0.000 description 1
- NRJQITNJATWTHX-UHFFFAOYSA-N C1=CC=C(/C2=[SiH]/[Mn]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Mn]3(C5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Mn]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC=C(/C2=[SiH]/[Mn]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Mn]3(C5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Mn]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Mn]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 NRJQITNJATWTHX-UHFFFAOYSA-N 0.000 description 1
- IDXKABVEHRTZOX-UHFFFAOYSA-N C1=CC=C(/C2=[SiH]/[Ni]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Ni]3(C5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Ni]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC=C(/C2=[SiH]/[Ni]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Ni]3(C5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Ni]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Ni]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 IDXKABVEHRTZOX-UHFFFAOYSA-N 0.000 description 1
- QSDYISLFVLXUPV-UHFFFAOYSA-N C1=CC=C(/C2=[SiH]/[Pd]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Pd]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Pd]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC=C(/C2=[SiH]/[Pd]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Pd]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Pd]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Pd]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 QSDYISLFVLXUPV-UHFFFAOYSA-N 0.000 description 1
- MHSLHKXQNMNYOE-UHFFFAOYSA-N C1=CC=C(/C2=[SiH]/[Pt]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Pt]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Pt]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC=C(/C2=[SiH]/[Pt]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Pt]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Pt]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Pt]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 MHSLHKXQNMNYOE-UHFFFAOYSA-N 0.000 description 1
- DVLRJAPWAHDDAH-UHFFFAOYSA-N C1=CC=C(/C2=[SiH]/[Zn]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Zn]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Zn]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 Chemical compound C1=CC=C(/C2=[SiH]/[Zn]34N5=CC=CC6=C5/C(=C\C=C/6)C5=N3C(=CC=C5)N(C3=CC=CC=C3)C3=CC=C5C=CC=C2C5=N34)C=C1.CN1C2=C(C=CC=C2)N2C3=CC=CC4=N3[Zn]3(N5C=N(C)C6=C5/C4=C\C=C/6)N4=C5C(=CC1=C24)/C=C\C=C/5[Si]3(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=C1/N(C)=C\C3[Zn]13C4=C(C=CC=C4)C4=COC5=C4N1=C1/C(=C\5)N(C)C4=C(C=CC=C4)N1C1=CC=CC2=N13.CN1C=C2C3=CC=CC=C3[Zn]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2N4=C53 DVLRJAPWAHDDAH-UHFFFAOYSA-N 0.000 description 1
- VEDHCCNBRJETIW-FLKWRGKHSA-N C1=CC=C(C2=CN(C3=C/C4=C(\C=C/3)C3=C(C=CC=C3)N4C3=CC=C4C(=C3)N(C3=CC=CC=N3)C3=C4C=CC=C3)N=C2)C=C1.C1=CC=C(C2=CN3C4=C5/C6=C(\C=C/4)C4=C(C=CC=C4)N6C4=CC=C6C7=C(C=CC=C7)N7C8=CC=CC=N8[Pd]5(C4=C67)N3=C2)C=C1.N=N/N=N/N=N/N=[Pd].N=N/N=N/N=N/N=[Pd] Chemical compound C1=CC=C(C2=CN(C3=C/C4=C(\C=C/3)C3=C(C=CC=C3)N4C3=CC=C4C(=C3)N(C3=CC=CC=N3)C3=C4C=CC=C3)N=C2)C=C1.C1=CC=C(C2=CN3C4=C5/C6=C(\C=C/4)C4=C(C=CC=C4)N6C4=CC=C6C7=C(C=CC=C7)N7C8=CC=CC=N8[Pd]5(C4=C67)N3=C2)C=C1.N=N/N=N/N=N/N=[Pd].N=N/N=N/N=N/N=[Pd] VEDHCCNBRJETIW-FLKWRGKHSA-N 0.000 description 1
- ZBHZPHWXYKHSJA-UHFFFAOYSA-N C1=CC=C(C2=CN3C4=C5C6=C(C=C4)C4=C(C=CC=C4)N6C4=CC=C6C7=C(C=CC=C7)N7C8=CC=CC=N8[Pd]5(C4=C67)N3=C2)C=C1.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC3=C2N4C2=C3C=CC=C2)C2=N1C=CC=C2.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC3=C2N4C2=C3C=CC=C2)N2C=CC=N21 Chemical compound C1=CC=C(C2=CN3C4=C5C6=C(C=C4)C4=C(C=CC=C4)N6C4=CC=C6C7=C(C=CC=C7)N7C8=CC=CC=N8[Pd]5(C4=C67)N3=C2)C=C1.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC3=C2N4C2=C3C=CC=C2)C2=N1C=CC=C2.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC3=C2N4C2=C3C=CC=C2)N2C=CC=N21 ZBHZPHWXYKHSJA-UHFFFAOYSA-N 0.000 description 1
- CUFIKEPCLBLEHU-UHFFFAOYSA-N C1=CC=C(C2=CN3C4=C5C6=C(C=C4)C4=C(C=CC=C4)N6C4=CC=C6C7=C(C=CC=C7)N7C8=CC=CC=N8[Pd]5(C4=C67)N3=C2)C=C1.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC3=C2N4C2=C3C=CC=C2)N2C=CC=N21.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC=C2)C2=C1C1=C(C=C2)C2=C(C=CC=C2)N41 Chemical compound C1=CC=C(C2=CN3C4=C5C6=C(C=C4)C4=C(C=CC=C4)N6C4=CC=C6C7=C(C=CC=C7)N7C8=CC=CC=N8[Pd]5(C4=C67)N3=C2)C=C1.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC3=C2N4C2=C3C=CC=C2)N2C=CC=N21.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21C2=C(C=CC=C2)C2=C1C1=C(C=C2)C2=C(C=CC=C2)N41 CUFIKEPCLBLEHU-UHFFFAOYSA-N 0.000 description 1
- FSRKAWCUZPALSP-UHFFFAOYSA-N C1=CC=C(C2=O[Ag]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=C\3C3=C(\C=C/7)OC=C23)/C5=C/64)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Ag]142)N3C.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Ag]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=C(C=CC=C6)[Ag]53N2=C1)O4 Chemical compound C1=CC=C(C2=O[Ag]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=C\3C3=C(\C=C/7)OC=C23)/C5=C/64)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Ag]142)N3C.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Ag]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=C(C=CC=C6)[Ag]53N2=C1)O4 FSRKAWCUZPALSP-UHFFFAOYSA-N 0.000 description 1
- MABGIUPHDFPMPK-UHFFFAOYSA-N C1=CC=C(C2=O[Au]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=C\3C3=C(\C=C/7)OC=C23)/C5=C/64)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Au]142)N3C.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Au]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=C(C=CC=C6)[Au]53N2=C1)O4 Chemical compound C1=CC=C(C2=O[Au]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=C\3C3=C(\C=C/7)OC=C23)/C5=C/64)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Au]142)N3C.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Au]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=C(C=CC=C6)[Au]53N2=C1)O4 MABGIUPHDFPMPK-UHFFFAOYSA-N 0.000 description 1
- SSJSYSVAVDCQIN-UHFFFAOYSA-O C1=CC=C(C2=O[Co]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Co]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Co]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Co]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=O[Co]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Co]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Co]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Co]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 SSJSYSVAVDCQIN-UHFFFAOYSA-O 0.000 description 1
- PIDBLIYWXNNGHB-UHFFFAOYSA-O C1=CC=C(C2=O[Cu]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Cu]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Cu]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Cu]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=O[Cu]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Cu]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Cu]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Cu]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 PIDBLIYWXNNGHB-UHFFFAOYSA-O 0.000 description 1
- HMKPHYMQJAUXHU-UHFFFAOYSA-N C1=CC=C(C2=O[Cu]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=C\3C3=C(\C=C/7)OC=C23)/C5=C/64)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Cu]142)N3C.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Cu]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=C(C=CC=C6)[Cu]53N2=C1)O4 Chemical compound C1=CC=C(C2=O[Cu]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=C\3C3=C(\C=C/7)OC=C23)/C5=C/64)C=C1.CC1=CC(C)=N2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Cu]142)N3C.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Cu]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(OC=C6C6=C(C=CC=C6)[Cu]53N2=C1)O4 HMKPHYMQJAUXHU-UHFFFAOYSA-N 0.000 description 1
- IXENRJVFHIBIFV-UHFFFAOYSA-O C1=CC=C(C2=O[Ir]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Ir]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Ir]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Ir]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=O[Ir]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Ir]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Ir]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Ir]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 IXENRJVFHIBIFV-UHFFFAOYSA-O 0.000 description 1
- NMSQWYHDGCSBSU-UHFFFAOYSA-O C1=CC=C(C2=O[Mn]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Mn]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Mn]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Mn]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 Chemical compound C1=CC=C(C2=O[Mn]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Mn]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Mn]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Mn]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 NMSQWYHDGCSBSU-UHFFFAOYSA-O 0.000 description 1
- AFFCBGWBCINVKY-UHFFFAOYSA-O C1=CC=C(C2=O[Ni]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Ni]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Ni]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Ni]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 Chemical compound C1=CC=C(C2=O[Ni]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Ni]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Ni]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Ni]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 AFFCBGWBCINVKY-UHFFFAOYSA-O 0.000 description 1
- HKIRTBZWTFVJGG-UHFFFAOYSA-O C1=CC=C(C2=O[Pd]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Pd]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Pd]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Pd]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 Chemical compound C1=CC=C(C2=O[Pd]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Pd]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Pd]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Pd]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 HKIRTBZWTFVJGG-UHFFFAOYSA-O 0.000 description 1
- AMKJQGBJZPNLJQ-UHFFFAOYSA-O C1=CC=C(C2=O[Pt]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Pt]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Pt]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Pt]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 Chemical compound C1=CC=C(C2=O[Pt]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Pt]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Pt]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Pt]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 AMKJQGBJZPNLJQ-UHFFFAOYSA-O 0.000 description 1
- LYFIVKXYPKUTGI-UHFFFAOYSA-O C1=CC=C(C2=O[Rh]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Rh]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Rh]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Rh]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=O[Rh]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\N3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Rh]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Rh]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Rh]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=N45 LYFIVKXYPKUTGI-UHFFFAOYSA-O 0.000 description 1
- HIZWYFXYJHQGQA-UHFFFAOYSA-O C1=CC=C(C2=O[Zn]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Zn]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Zn]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Zn]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 Chemical compound C1=CC=C(C2=O[Zn]34/C5=C(/C=C\C6=C5C2=CO6)N2C5=C(C=CC=C5)C5=C/C6=CC=CC(=C6\C3=C/52)C2=CC=CC=N24)C=C1.C1=CC=C([PH]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Zn]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Zn]124.CN1C2=CC3=C4C(=CC=C3)C3=N(OC5=C3C=CC=C5)[Zn]35C6=C(OC7=C6C(=CO7)C6=CC=CC=N63)N(C3=C1C=CC=C3)C2=C45 HIZWYFXYJHQGQA-UHFFFAOYSA-O 0.000 description 1
- XMJOJNFTFPZLIB-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Ag]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N3C3=C(C=C7)O/C=C/23)/C5=C/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Ag]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=C4C5=C(/C=C/31)/C=C/C=C5/C1=C(OC3=C1C=CC=C3)[Ag]/41C3=CC=CC=C3C3=COC4=C3/N1=C/2O4 Chemical compound C1=CC=C(C2=[SiH][Ag]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N3C3=C(C=C7)O/C=C/23)/C5=C/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Ag]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=C4C5=C(/C=C/31)/C=C/C=C5/C1=C(OC3=C1C=CC=C3)[Ag]/41C3=CC=CC=C3C3=COC4=C3/N1=C/2O4 XMJOJNFTFPZLIB-UHFFFAOYSA-N 0.000 description 1
- BLFYVJGWGOONJS-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Au]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N3C3=C(C=C7)O/C=C/23)/C5=C/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Au]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=C4C5=C(/C=C/31)/C=C/C=C5/C1=C(OC3=C1C=CC=C3)[Au]/41C3=CC=CC=C3C3=COC4=C3/N1=C/2O4 Chemical compound C1=CC=C(C2=[SiH][Au]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N3C3=C(C=C7)O/C=C/23)/C5=C/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Au]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=C4C5=C(/C=C/31)/C=C/C=C5/C1=C(OC3=C1C=CC=C3)[Au]/41C3=CC=CC=C3C3=COC4=C3/N1=C/2O4 BLFYVJGWGOONJS-UHFFFAOYSA-N 0.000 description 1
- JYOCWJCPPHAOTF-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Co]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Co]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Co]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Co]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=[SiH][Co]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Co]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Co]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Co]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 JYOCWJCPPHAOTF-UHFFFAOYSA-N 0.000 description 1
- IFRGAXJRQBCSGB-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Cu]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N3C3=C(C=C7)O/C=C/23)/C5=C/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Cu]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=C4C5=C(/C=C/31)/C=C/C=C5/C1=C(OC3=C1C=CC=C3)[Cu]/41C3=CC=CC=C3C3=COC4=C3/N1=C/2O4 Chemical compound C1=CC=C(C2=[SiH][Cu]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N3C3=C(C=C7)O/C=C/23)/C5=C/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Cu]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)N2C3=C4C5=C(/C=C/31)/C=C/C=C5/C1=C(OC3=C1C=CC=C3)[Cu]/41C3=CC=CC=C3C3=COC4=C3/N1=C/2O4 IFRGAXJRQBCSGB-UHFFFAOYSA-N 0.000 description 1
- RGULSXNBUKMFCC-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Cu]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Cu]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Cu]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Cu]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=[SiH][Cu]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Cu]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Cu]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Cu]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 RGULSXNBUKMFCC-UHFFFAOYSA-N 0.000 description 1
- OBXUKLGFHUIQJS-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Ir]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Ir]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Ir]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Ir]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=[SiH][Ir]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Ir]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Ir]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Ir]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 OBXUKLGFHUIQJS-UHFFFAOYSA-N 0.000 description 1
- KVZACUCZWREHHR-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Mn]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Mn]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Mn]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Mn]53C2=C1)O4 Chemical compound C1=CC=C(C2=[SiH][Mn]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Mn]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Mn]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Mn]53C2=C1)O4 KVZACUCZWREHHR-UHFFFAOYSA-N 0.000 description 1
- HIKQFHISUCEWBN-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Ni]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Ni]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Ni]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Ni]53C2=C1)O4 Chemical compound C1=CC=C(C2=[SiH][Ni]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Ni]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Ni]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Ni]53C2=C1)O4 HIKQFHISUCEWBN-UHFFFAOYSA-N 0.000 description 1
- SXUHHVLZUOJZHP-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Pd]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Pd]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Pd]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Pd]53C2=C1)O4 Chemical compound C1=CC=C(C2=[SiH][Pd]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Pd]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Pd]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Pd]53C2=C1)O4 SXUHHVLZUOJZHP-UHFFFAOYSA-N 0.000 description 1
- JBXMECJUDCINPQ-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Pt]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Pt]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Pt]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Pt]53C2=C1)O4 Chemical compound C1=CC=C(C2=[SiH][Pt]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Pt]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Pt]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Pt]53C2=C1)O4 JBXMECJUDCINPQ-UHFFFAOYSA-N 0.000 description 1
- IQJHNCRVVGEHJE-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Rh]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Rh]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Rh]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Rh]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 Chemical compound C1=CC=C(C2=[SiH][Rh]34N5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)/C3=C/C=C\C4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Rh]32N2=CC=CC=C72)C=C1.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)OC=C5C3=N(C=C5C=CC=CC5=C3)[Rh]241.CN1C2=CC3=C4C(=CC=C3)C3=C(OC5=C3C=CC=C5)[Rh]35N6=CC=CC=C6C6=COC7=C6N3=C(O7)N(C3=C1C=CC=C3)C2=N45 IQJHNCRVVGEHJE-UHFFFAOYSA-N 0.000 description 1
- SCXZDNDUUYQSDM-UHFFFAOYSA-N C1=CC=C(C2=[SiH][Zn]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Zn]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Zn]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Zn]53C2=C1)O4 Chemical compound C1=CC=C(C2=[SiH][Zn]34C5=CC=CC=C5C5=C6C(=CC=C5)/C=C5/C7=C(C=CC=C7)N(C7=N\3C3=C(\C=C/7)OC=C23)/C5=N/64)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5C5=C(C=CC=C5CC6)[Zn]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Zn]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C6=C(OC=C6C6=C(C=CC=C6)[Zn]53C2=C1)O4 SCXZDNDUUYQSDM-UHFFFAOYSA-N 0.000 description 1
- HGNUOLSQTXMZHM-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Ag]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=C2[Ag]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N32)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Ag]35C2=C1 Chemical compound C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Ag]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=C2[Ag]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N32)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Ag]35C2=C1 HGNUOLSQTXMZHM-UHFFFAOYSA-N 0.000 description 1
- CIUIWUIYJXOBBH-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Au]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=C2[Au]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N32)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Au]35C2=C1 Chemical compound C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Au]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=C2[Au]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N32)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Au]35C2=C1 CIUIWUIYJXOBBH-UHFFFAOYSA-N 0.000 description 1
- PWNHORVJQCYTIY-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Cu]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=C2[Cu]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N32)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Cu]35C2=C1 Chemical compound C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Cu]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=C2[Cu]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N32)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Cu]35C2=C1 PWNHORVJQCYTIY-UHFFFAOYSA-N 0.000 description 1
- VHXGGFRHMKXDPH-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=N5[Ag]43C4=CC=CC=C4C4=COC5=C4/C3=C/2O5)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Ag]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Ag]62/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/N(=C\C=C/5)[Ag]241 Chemical compound C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=N5[Ag]43C4=CC=CC=C4C4=COC5=C4/C3=C/2O5)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Ag]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Ag]62/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/N(=C\C=C/5)[Ag]241 VHXGGFRHMKXDPH-UHFFFAOYSA-N 0.000 description 1
- AIEPWRRHVHOGKQ-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=N5[Au]43C4=CC=CC=C4C4=COC5=C4/C3=C/2O5)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Au]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Au]62/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/N(=C\C=C/5)[Au]241 Chemical compound C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=N5[Au]43C4=CC=CC=C4C4=COC5=C4/C3=C/2O5)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Au]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Au]62/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/N(=C\C=C/5)[Au]241 AIEPWRRHVHOGKQ-UHFFFAOYSA-N 0.000 description 1
- GETNJNNSUHDXMF-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=N5[Cu]43C4=CC=CC=C4C4=COC5=C4/C3=C/2O5)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Cu]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Cu]62/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/N(=C\C=C/5)[Cu]241 Chemical compound C1=CC=C(N2C3=C4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=N5[Cu]43C4=CC=CC=C4C4=COC5=C4/C3=C/2O5)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Cu]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=C(C=CC=C5)[Cu]62/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/N(=C\C=C/5)[Cu]241 GETNJNNSUHDXMF-UHFFFAOYSA-N 0.000 description 1
- MNMJAIUWEDYRIF-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Co]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Co]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Co]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Co]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Co]432 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Co]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Co]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Co]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Co]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Co]432 MNMJAIUWEDYRIF-UHFFFAOYSA-N 0.000 description 1
- HUNPDVSTRZRGBC-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Cu]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Cu]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Cu]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Cu]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Cu]432 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Cu]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Cu]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Cu]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Cu]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Cu]432 HUNPDVSTRZRGBC-UHFFFAOYSA-N 0.000 description 1
- XHZLSHSJIKJYSF-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Ir]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ir]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ir]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Ir]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Ir]432 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Ir]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ir]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ir]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Ir]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Ir]432 XHZLSHSJIKJYSF-UHFFFAOYSA-N 0.000 description 1
- ONQUPGDOHKYSDT-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Mn]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Mn]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Mn]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Mn]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Mn]342 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Mn]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Mn]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Mn]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Mn]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Mn]342 ONQUPGDOHKYSDT-UHFFFAOYSA-N 0.000 description 1
- CBKBJTDSPINIJJ-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Ni]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ni]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ni]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Ni]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Ni]342 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Ni]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ni]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Ni]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Ni]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Ni]342 CBKBJTDSPINIJJ-UHFFFAOYSA-N 0.000 description 1
- JBRWDKIWXWYIHQ-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Pd]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pd]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pd]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Pd]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pd]342 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Pd]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pd]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pd]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Pd]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pd]342 JBRWDKIWXWYIHQ-UHFFFAOYSA-N 0.000 description 1
- IMHNNMRKEOFNDJ-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Pt]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pt]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pt]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Pt]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pt]342 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Pt]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pt]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Pt]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Pt]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pt]342 IMHNNMRKEOFNDJ-UHFFFAOYSA-N 0.000 description 1
- UBAGHDMERKGEJC-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Rh]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Rh]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Rh]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Rh]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Rh]432 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Rh]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Rh]62/N3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Rh]62N3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Rh]324.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Rh]432 UBAGHDMERKGEJC-UHFFFAOYSA-N 0.000 description 1
- RHNWSMHBKAMNPW-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Zn]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Zn]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Zn]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Zn]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Zn]342 Chemical compound C1=CC=C(N2C3=C4C5=C(OC=C5C5=CC=CC=N5[Zn]45C4=C2/C=C/C2=C\4C4=C(/C=C\C6=C/4N5=CS6)CC2)O3)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Zn]62/C3=C/14.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=C6C(=CC=C5)C5=N(C=CC=C5)[Zn]62C3=C14.C1=CC=N2C(=C1)C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Zn]342.CC1=CC(C)=N2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Zn]342 RHNWSMHBKAMNPW-UHFFFAOYSA-N 0.000 description 1
- CSRXXMLHVOHIBX-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(\C=C/3)CCC3=C\5C5=C(\C=C/3)SC=C5[Ag]43C4=CC=CC=C4C4=COC5=C4N3=C2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ag]26/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Ag]241 Chemical compound C1=CC=C(N2C3=C4C5=C(\C=C/3)CCC3=C\5C5=C(\C=C/3)SC=C5[Ag]43C4=CC=CC=C4C4=COC5=C4N3=C2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ag]26/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Ag]241 CSRXXMLHVOHIBX-UHFFFAOYSA-N 0.000 description 1
- QMAYKEQCGQAMFM-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(\C=C/3)CCC3=C\5C5=C(\C=C/3)SC=C5[Au]43C4=CC=CC=C4C4=COC5=C4N3=C2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Au]26/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Au]241 Chemical compound C1=CC=C(N2C3=C4C5=C(\C=C/3)CCC3=C\5C5=C(\C=C/3)SC=C5[Au]43C4=CC=CC=C4C4=COC5=C4N3=C2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Au]26/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Au]241 QMAYKEQCGQAMFM-UHFFFAOYSA-N 0.000 description 1
- OQINYYXXOROWEK-UHFFFAOYSA-N C1=CC=C(N2C3=C4C5=C(\C=C/3)CCC3=C\5C5=C(\C=C/3)SC=C5[Cu]43C4=CC=CC=C4C4=COC5=C4N3=C2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Cu]26/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Cu]241 Chemical compound C1=CC=C(N2C3=C4C5=C(\C=C/3)CCC3=C\5C5=C(\C=C/3)SC=C5[Cu]43C4=CC=CC=C4C4=COC5=C4N3=C2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Cu]26/C3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Cu]241 OQINYYXXOROWEK-UHFFFAOYSA-N 0.000 description 1
- KVQUSFJUBKMXQI-UHFFFAOYSA-N C1=CC=C(N2C3=CC(N4C5=C(C=CC=C5)C5=C4/C=C(N4C=CC=N4)\C=C/5)=CC=C3C3=C2C=CC=C3)N=C1.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21/C2=C(/C=C\C3=C2N4C2=C3C=CC=C2)N2C=CC=N21.NN=[Pd].NN=[Pd] Chemical compound C1=CC=C(N2C3=CC(N4C5=C(C=CC=C5)C5=C4/C=C(N4C=CC=N4)\C=C/5)=CC=C3C3=C2C=CC=C3)N=C1.C1=CC=N2C(=C1)N1C3=C(C=CC=C3)C3=CC=C4C(=C31)[Pd]21/C2=C(/C=C\C3=C2N4C2=C3C=CC=C2)N2C=CC=N21.NN=[Pd].NN=[Pd] KVQUSFJUBKMXQI-UHFFFAOYSA-N 0.000 description 1
- AYLHURMTVAXQPU-UHFFFAOYSA-N C1=CC=C(N2C3=CC=CC4=N3[Au]3(/C5=C/C=C/C=C\45)/C4=C\2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)/C=C\2)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=C(C=CC=C6)[Au]4(C4/C=N(/C)C1=C24)N7=C53.CN1C=C2C3=CC=CC=C3[Au]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Au]3(/C5=C/C=C/C=C\45)/C4=C\2SC2=C4C(=CC=C2)C2=N3C3=C(C=CC=C3)/C=C\2)C=C1.CN1C=C2C3=C4C(=CC=C3)N3C5=C(C=CC=C5)N(C)C5=CC6=C7C(=CO6)C6=C(C=CC=C6)[Au]4(C4/C=N(/C)C1=C24)N7=C53.CN1C=C2C3=CC=CC=C3[Au]34C5=CC=CC6=C5N(C=C6)C5=N3C(=CC=C5)N3C5=C(C=CC=C5)C5=CC1=C2C4=C53 AYLHURMTVAXQPU-UHFFFAOYSA-N 0.000 description 1
- KPWVLPUZOBDRPM-WERRTIIWSA-N C1=CC=C(N2C3=CC=CC4=N3[Co]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Co]231.CN1C2=C(C=CC=C2)C2=C1[Co]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Co]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Co]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Co]231.CN1C2=C(C=CC=C2)C2=C1[Co]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Co]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 KPWVLPUZOBDRPM-WERRTIIWSA-N 0.000 description 1
- XNFWPRHNIUPLGL-WERRTIIWSA-N C1=CC=C(N2C3=CC=CC4=N3[Cu]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Cu]231.CN1C2=C(C=CC=C2)C2=C1[Cu]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Cu]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Cu]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Cu]231.CN1C2=C(C=CC=C2)C2=C1[Cu]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Cu]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 XNFWPRHNIUPLGL-WERRTIIWSA-N 0.000 description 1
- NZZKGWKHNVKCOR-WERRTIIWSA-N C1=CC=C(N2C3=CC=CC4=N3[Ir]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Ir]231.CN1C2=C(C=CC=C2)C2=C1[Ir]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Ir]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Ir]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Ir]231.CN1C2=C(C=CC=C2)C2=C1[Ir]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Ir]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 NZZKGWKHNVKCOR-WERRTIIWSA-N 0.000 description 1
- BASXIDDMWBLZNR-UIGSTKRTSA-N C1=CC=C(N2C3=CC=CC4=N3[Mn]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Mn]231.CN1=CC2C3=C1N(C)=CN3C1=N3C(=CC=C1)N(C1=CC=CC=C1)C/N1=C/C4=COC5=C4/N(=C\O5)[Mn]231.CN1C2=C(C=CC=C2)C2=C1[Mn]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Mn]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Mn]231.CN1=CC2C3=C1N(C)=CN3C1=N3C(=CC=C1)N(C1=CC=CC=C1)C/N1=C/C4=COC5=C4/N(=C\O5)[Mn]231.CN1C2=C(C=CC=C2)C2=C1[Mn]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4 BASXIDDMWBLZNR-UIGSTKRTSA-N 0.000 description 1
- MUOTZCJNVSXLJF-PDHBBINHSA-N C1=CC=C(N2C3=CC=CC4=N3[Ni]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Ni]231.CN1C2=C(C=CC=C2)C2=C1[Ni]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C1N(C)=CC3[Ni]13/C4=C/OC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Ni]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Ni]231.CN1C2=C(C=CC=C2)C2=C1[Ni]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C1N(C)=CC3[Ni]13/C4=C/OC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 MUOTZCJNVSXLJF-PDHBBINHSA-N 0.000 description 1
- BDAZRPURINQIKW-WERRTIIWSA-N C1=CC=C(N2C3=CC=CC4=N3[Pd]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Pd]231.CN1C2=C(C=CC=C2)C2=C1[Pd]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C1N(C)=CC3[Pd]13N4=C2C=CC=C4N(C2=CC=CC=C2)C/N1=C/C1=COC2=C1/N3=C\O2 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Pd]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Pd]231.CN1C2=C(C=CC=C2)C2=C1[Pd]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C1N(C)=CC3[Pd]13N4=C2C=CC=C4N(C2=CC=CC=C2)C/N1=C/C1=COC2=C1/N3=C\O2 BDAZRPURINQIKW-WERRTIIWSA-N 0.000 description 1
- HMXWODYLCTVRRJ-ZSEBHHAASA-N C1=CC=C(N2C3=CC=CC4=N3[Pt]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Pt]231.CN1=CC2C3=C1N(C)=CN3[Pt]13N4=C2C=CC=C4N(C2=CC=CC=C2)C/N1=C/C1=COC2=C1/N3=C\O2.CN1C2=C(C=CC=C2)C2=C1[Pt]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Pt]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Pt]231.CN1=CC2C3=C1N(C)=CN3[Pt]13N4=C2C=CC=C4N(C2=CC=CC=C2)C/N1=C/C1=COC2=C1/N3=C\O2.CN1C2=C(C=CC=C2)C2=C1[Pt]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4 HMXWODYLCTVRRJ-ZSEBHHAASA-N 0.000 description 1
- ATJXYUZDRLSVDS-WERRTIIWSA-N C1=CC=C(N2C3=CC=CC4=N3[Rh]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Rh]231.CN1C2=C(C=CC=C2)C2=C1[Rh]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Rh]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Rh]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=N(C=CC=C4)[Rh]231.CN1C2=C(C=CC=C2)C2=C1[Rh]13N4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1N3=C2O4.CN1C=C2C3=C1/N(C)=C\N3[Rh]13C4=COC5=C4C(=CO5)/C=N\1CN(C1=CC=CC=C1)C1=CC=CC2=N13 ATJXYUZDRLSVDS-WERRTIIWSA-N 0.000 description 1
- KHXKLSUTJDWYNJ-ZSEBHHAASA-N C1=CC=C(N2C3=CC=CC4=N3[Zn]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Zn]231.CN1=CC2C3=C1N(C)=CN3[Zn]13N4=C2C=CC=C4N(C2=CC=CC=C2)C/N1=C/C1=COC2=C1/N3=C\O2.CN1C2=C(C=CC=C2)C2=C1[Zn]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4 Chemical compound C1=CC=C(N2C3=CC=CC4=N3[Zn]3(C5=CC=CC6=C5N(/C=C\6)C5=N3C2=CC=C5)/C2=C/OC3=CC=CC4=C32)C=C1.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C(\C=C/4)C4=C(C=CC=C4)[Zn]231.CN1=CC2C3=C1N(C)=CN3[Zn]13N4=C2C=CC=C4N(C2=CC=CC=C2)C/N1=C/C1=COC2=C1/N3=C\O2.CN1C2=C(C=CC=C2)C2=C1[Zn]13C4=CC=CN4C4=N1C(=CC=C4)N1C=CC4=C1/N3=C/2O4 KHXKLSUTJDWYNJ-ZSEBHHAASA-N 0.000 description 1
- QXHIMGPSUMJDLD-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Mn]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Mn]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Mn]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Mn]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Mn]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Mn]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Mn]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Mn]53C2=C1 QXHIMGPSUMJDLD-UHFFFAOYSA-N 0.000 description 1
- CTRHSSUKIGBDKN-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Ni]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Ni]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Ni]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Ni]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Ni]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Ni]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Ni]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Ni]53C2=C1 CTRHSSUKIGBDKN-UHFFFAOYSA-N 0.000 description 1
- GHUZHZBBDVLUPD-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Pd]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Pd]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Pd]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Pd]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Pd]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Pd]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Pd]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Pd]53C2=C1 GHUZHZBBDVLUPD-UHFFFAOYSA-N 0.000 description 1
- HNIFQSXISRLNSB-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Pt]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Pt]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Pt]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Pt]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Pt]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Pt]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Pt]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Pt]53C2=C1 HNIFQSXISRLNSB-UHFFFAOYSA-N 0.000 description 1
- WDSRUEIARYGWKO-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Zn]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Zn]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Zn]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Zn]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C(=CC=C3)[Zn]43C4=C5C=CC=CC5=CN4C4=CSC5=C4/N3=C/2S5)C=C1.CC1(C)C2=CC=CC3=N2[Zn]2(/C4=C/C=C\C5=C4C(=CC=C5)C4=N2C2=C(C=C4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1=CC2C3=C1/C=C\C=C/3C1=N3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=N4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Zn]234.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4C(=CS6)[Zn]53C2=C1 WDSRUEIARYGWKO-UHFFFAOYSA-N 0.000 description 1
- ZBJBBRPUIOIARF-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Mn]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Mn]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Mn]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Mn]241 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Mn]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Mn]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Mn]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Mn]241 ZBJBBRPUIOIARF-UHFFFAOYSA-N 0.000 description 1
- FWHNXCPKQDEWBD-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Ni]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ni]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ni]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Ni]241 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Ni]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ni]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ni]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Ni]241 FWHNXCPKQDEWBD-UHFFFAOYSA-N 0.000 description 1
- JSZMJWXSESGIDB-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Pd]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pd]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pd]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Pd]241 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Pd]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pd]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pd]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Pd]241 JSZMJWXSESGIDB-UHFFFAOYSA-N 0.000 description 1
- CYCYCLVPANFGEQ-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Pt]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pt]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pt]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Pt]241 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Pt]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pt]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Pt]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Pt]241 CYCYCLVPANFGEQ-UHFFFAOYSA-N 0.000 description 1
- DZEWOQBIZYSZSN-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Zn]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Zn]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Zn]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Zn]241 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5C5=C(/C=C\3)SC=C5[Zn]43C4=CC=CC=C4C4=COC5=C4/N3=C/2O5)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Zn]26/N3=C/14.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Zn]26/N3=C/14.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3/C(=C\C=C/5)[Zn]241 DZEWOQBIZYSZSN-UHFFFAOYSA-N 0.000 description 1
- SHOKXXQAWOPGQC-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Co]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Co]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Co]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Co]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Co]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Co]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Co]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Co]53C2=C1 SHOKXXQAWOPGQC-UHFFFAOYSA-N 0.000 description 1
- BEDZIVGVGZQFLL-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Cu]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Cu]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Cu]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Cu]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Cu]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Cu]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Cu]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Cu]53C2=C1 BEDZIVGVGZQFLL-UHFFFAOYSA-N 0.000 description 1
- LVYZIDMTNOFHAM-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ir]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Ir]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Ir]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ir]53C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ir]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Ir]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Ir]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ir]53C2=C1 LVYZIDMTNOFHAM-UHFFFAOYSA-N 0.000 description 1
- YJBZOTFLVIJXOH-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Rh]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Rh]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Rh]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ir]53=C2=C1 Chemical compound C1=CC=C(N2C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Rh]43C4=C5C=CC=CC5=CN4C4=CSC5=C4N3=C2S5)C=C1.CC1(C)C2=CC=CC3=N2[Rh]2(N4=CC=CC5=C4C(=C\C=C/5)/C4=N\2C2=C(\C=C/4)CCC4=C(C=CC=C4)N23)[Si]1(C1=CC=CC=C1)C1=CC=CC=C1.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3C(=CC=C5)[Rh]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=N5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ir]53=C2=C1 YJBZOTFLVIJXOH-UHFFFAOYSA-N 0.000 description 1
- IBZXVEDTTGOVMD-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Co]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Co]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Co]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Co]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Co]324 Chemical compound C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Co]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Co]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Co]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Co]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Co]324 IBZXVEDTTGOVMD-UHFFFAOYSA-N 0.000 description 1
- NVENKYJKMLTUMB-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Cu]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Cu]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Cu]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Cu]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Cu]324 Chemical compound C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Cu]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Cu]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Cu]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Cu]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Cu]324 NVENKYJKMLTUMB-UHFFFAOYSA-N 0.000 description 1
- CYCLFJQLCWAGGA-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Ir]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Ir]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Ir]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Ir]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ir]324 Chemical compound C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Ir]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Ir]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Ir]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Ir]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ir]324 CYCLFJQLCWAGGA-UHFFFAOYSA-N 0.000 description 1
- LAWFUPQSKMRRBZ-UHFFFAOYSA-N C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Rh]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Rh]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Rh]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Rh]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Rh]324 Chemical compound C1=CC=C(N2C3=N4C5=C(OC=C5C5=CC=CC=C5[Rh]45N4=CSC6=C4C4=C(\C=C/6)CCC6=C\4N\5=C2\C=C\6)O3)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Rh]26/N3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=N(SC5=C1C=CC=C5)[Rh]234.C1=CC=N2C(=C1)C1=C3C(=CC=C1)C=C1C4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=N(C=CC=C5)[Rh]26N3=C14.CC1=CC(C)=N2N1C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Rh]324 LAWFUPQSKMRRBZ-UHFFFAOYSA-N 0.000 description 1
- AWWZWGRCLFQHNT-UHFFFAOYSA-N C1=CC=C(N2CC3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Ag]34C3=CC=CN3C3=COC5=C3/N4=C/2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=C3C4=C(C=C1)N(C)C1=C(C=CC=C1)N4C1=N4C5=C(/C=C\C=C/5N1C)C1=CC=CC=C1[Ag]234.CN1C=CC2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4/C(=C\C=C/5)[Ag]213 Chemical compound C1=CC=C(N2CC3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Ag]34C3=CC=CN3C3=COC5=C3/N4=C/2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=C3C4=C(C=C1)N(C)C1=C(C=CC=C1)N4C1=N4C5=C(/C=C\C=C/5N1C)C1=CC=CC=C1[Ag]234.CN1C=CC2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4/C(=C\C=C/5)[Ag]213 AWWZWGRCLFQHNT-UHFFFAOYSA-N 0.000 description 1
- OKKHCDFGAXEPID-UHFFFAOYSA-N C1=CC=C(N2CC3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Cu]34C3=CC=CN3C3=COC5=C3/N4=C/2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=C3C4=C(C=C1)N(C)C1=C(C=CC=C1)N4C1=N4C5=C(/C=C\C=C/5N1C)C1=CC=CC=C1[Cu]234.CN1C=CC2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4/C(=C\C=C/5)[Cu]213 Chemical compound C1=CC=C(N2CC3(C4=CC=CC=C4)CC4=C(C=CC=C4)[Cu]34C3=CC=CN3C3=COC5=C3/N4=C/2O5)C=C1.CN1C=C2C3=C(C=CC=C31)C1=C3C4=C(C=C1)N(C)C1=C(C=CC=C1)N4C1=N4C5=C(/C=C\C=C/5N1C)C1=CC=CC=C1[Cu]234.CN1C=CC2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4/C(=C\C=C/5)[Cu]213 OKKHCDFGAXEPID-UHFFFAOYSA-N 0.000 description 1
- VPQVFFSFIYHUBK-UHFFFAOYSA-N C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Mn]72N3=C56)S4)C=C1 Chemical compound C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Mn]72N3=C56)S4)C=C1 VPQVFFSFIYHUBK-UHFFFAOYSA-N 0.000 description 1
- DYNMKONIUJBGLN-UHFFFAOYSA-N C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Ni]72N3=C56)S4)C=C1 Chemical compound C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Ni]72N3=C56)S4)C=C1 DYNMKONIUJBGLN-UHFFFAOYSA-N 0.000 description 1
- JBXOKPBCNAGMPP-UHFFFAOYSA-N C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Pd]72N3=C56)S4)C=C1 Chemical compound C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Pd]72N3=C56)S4)C=C1 JBXOKPBCNAGMPP-UHFFFAOYSA-N 0.000 description 1
- YKUGAIBMBIDMQY-UHFFFAOYSA-N C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Pt]72N3=C56)S4)C=C1 Chemical compound C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Pt]72N3=C56)S4)C=C1 YKUGAIBMBIDMQY-UHFFFAOYSA-N 0.000 description 1
- ZGGHQFYMDRSQAE-UHFFFAOYSA-N C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Zn]72N3=C56)S4)C=C1 Chemical compound C1=CC=C([Ge]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7N7=C(C=C8)C8=CC=CC=C8[Zn]72N3=C56)S4)C=C1 ZGGHQFYMDRSQAE-UHFFFAOYSA-N 0.000 description 1
- PFEKPOCMHJOTKF-UHFFFAOYSA-P C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Ag]32C2=CC=CC=C27)C=C1.CC1=CC(C)=C2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Ag]142)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Ag]35C4=C2N(C2=C1C=CC=C2)/C1=C\3C2=C(OC=C2C2=CC=CC=N25)O1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ag]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Ag]32C2=CC=CC=C27)C=C1.CC1=CC(C)=C2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Ag]142)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Ag]35C4=C2N(C2=C1C=CC=C2)/C1=C\3C2=C(OC=C2C2=CC=CC=N25)O1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ag]53N2=C1 PFEKPOCMHJOTKF-UHFFFAOYSA-P 0.000 description 1
- KWBZBKDUSYWLRX-UHFFFAOYSA-P C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Au]32C2=CC=CC=C27)C=C1.CC1=CC(C)=C2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Au]142)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Au]35C4=C2N(C2=C1C=CC=C2)/C1=C\3C2=C(OC=C2C2=CC=CC=N25)O1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Au]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Au]32C2=CC=CC=C27)C=C1.CC1=CC(C)=C2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Au]142)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Au]35C4=C2N(C2=C1C=CC=C2)/C1=C\3C2=C(OC=C2C2=CC=CC=N25)O1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Au]53N2=C1 KWBZBKDUSYWLRX-UHFFFAOYSA-P 0.000 description 1
- AYPKUXHEPOSIMX-UHFFFAOYSA-P C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Cu]32C2=CC=CC=C27)C=C1.CC1=CC(C)=C2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]142)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Cu]35C4=C2N(C2=C1C=CC=C2)/C1=C\3C2=C(OC=C2C2=CC=CC=N25)O1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)C3=CC=CC4=C3C3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\C(=C/54)[Cu]32C2=CC=CC=C27)C=C1.CC1=CC(C)=C2N1C1=COC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]142)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Cu]35C4=C2N(C2=C1C=CC=C2)/C1=C\3C2=C(OC=C2C2=CC=CC=N25)O1.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]53N2=C1 AYPKUXHEPOSIMX-UHFFFAOYSA-P 0.000 description 1
- UGMNOKCZCDXCJP-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Ag]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C3[Ag]23C2=C(C=CC=C2)C2=C3C3=C(C=C2)CCC2=C(C=CC=C2)N13.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Ag]312.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=C3[Ag]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=C\53)N2=CN(C)C3=C/C=C/C1=C\32 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Ag]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C3[Ag]23C2=C(C=CC=C2)C2=C3C3=C(C=C2)CCC2=C(C=CC=C2)N13.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Ag]312.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=C3[Ag]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=C\53)N2=CN(C)C3=C/C=C/C1=C\32 UGMNOKCZCDXCJP-UHFFFAOYSA-O 0.000 description 1
- UKAPNIYQPSFLRV-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Au]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C3[Au]23C2=C(C=CC=C2)C2=C3C3=C(C=C2)CCC2=C(C=CC=C2)N13.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Au]312.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=C3[Au]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=C\53)N2=CN(C)C3=C/C=C/C1=C\32 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Au]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C3[Au]23C2=C(C=CC=C2)C2=C3C3=C(C=C2)CCC2=C(C=CC=C2)N13.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Au]312.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=C3[Au]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=C\53)N2=CN(C)C3=C/C=C/C1=C\32 UKAPNIYQPSFLRV-UHFFFAOYSA-O 0.000 description 1
- PWKVQPQCJGQUQY-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Cu]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C3[Cu]23C2=C(C=CC=C2)C2=C3C3=C(C=C2)CCC2=C(C=CC=C2)N13.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Cu]312.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=C3[Cu]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=C\53)N2=CN(C)C3=C/C=C/C1=C\32 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/C3=C5/N(C6=CC=CC7=C6[Cu]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=N2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C3[Cu]23C2=C(C=CC=C2)C2=C3C3=C(C=C2)CCC2=C(C=CC=C2)N13.C1=CC=N2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/C1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Cu]312.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=C3[Cu]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=C\53)N2=CN(C)C3=C/C=C/C1=C\32 PWKVQPQCJGQUQY-UHFFFAOYSA-O 0.000 description 1
- PMGAVWZGWGUUGX-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Ag]23C2=COC5=C2C(=CC=C5)C2=C3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Ag]45N4/C=N(/C)C1=C24)O3 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Ag]23C2=COC5=C2C(=CC=C5)C2=C3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Ag]45N4/C=N(/C)C1=C24)O3 PMGAVWZGWGUUGX-UHFFFAOYSA-O 0.000 description 1
- KQGXHZMMFOGCHJ-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Au]23C2=COC5=C2C(=CC=C5)C2=C3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Au]45N4/C=N(/C)C1=C24)O3 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Au]23C2=COC5=C2C(=CC=C5)C2=C3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Au]45N4/C=N(/C)C1=C24)O3 KQGXHZMMFOGCHJ-UHFFFAOYSA-O 0.000 description 1
- MTJCCKAXUAXEOV-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Co]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Co]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Co]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Co]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Co]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Co]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Co]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Co]53N2=C1 MTJCCKAXUAXEOV-UHFFFAOYSA-Q 0.000 description 1
- XWOQYKDQOZDENF-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Cu]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Cu]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]53N2=C1 XWOQYKDQOZDENF-UHFFFAOYSA-Q 0.000 description 1
- BTOCNAFPUFBQIY-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Cu]23C2=COC5=C2C(=CC=C5)C2=C3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]45N4/C=N(/C)C1=C24)O3 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Cu]23C2=COC5=C2C(=CC=C5)C2=C3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]45N4/C=N(/C)C1=C24)O3 BTOCNAFPUFBQIY-UHFFFAOYSA-O 0.000 description 1
- SQUVLDOZTWETJS-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Ir]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Ir]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Ir]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Ir]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Ir]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Ir]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]53N2=C1 SQUVLDOZTWETJS-UHFFFAOYSA-Q 0.000 description 1
- JHRKCIFEKBCFKP-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Mn]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Mn]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Mn]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Mn]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Mn]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Mn]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Mn]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Mn]53N2=C1 JHRKCIFEKBCFKP-UHFFFAOYSA-Q 0.000 description 1
- SLPKGFGRMOVLHR-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Ni]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Ni]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Ni]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Ni]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Ni]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Ni]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Ni]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Ni]53N2=C1 SLPKGFGRMOVLHR-UHFFFAOYSA-Q 0.000 description 1
- GCLKQLKWHHSYLS-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Pd]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Pd]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Pd]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Pd]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Pd]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Pd]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Pd]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Pd]53N2=C1 GCLKQLKWHHSYLS-UHFFFAOYSA-Q 0.000 description 1
- JNHJDPUTTJLNFF-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Pt]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Pt]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Pt]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Pt]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Pt]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Pt]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Pt]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Pt]53N2=C1 JNHJDPUTTJLNFF-UHFFFAOYSA-Q 0.000 description 1
- LNZWLZHRZYXMLR-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Rh]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Rh]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Rh]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Rh]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Rh]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Rh]421)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Rh]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Rh]53N2=C1 LNZWLZHRZYXMLR-UHFFFAOYSA-Q 0.000 description 1
- WIFNMGMDQUMBOA-UHFFFAOYSA-Q C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Zn]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Zn]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Zn]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Zn]53N2=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)SC4=C3[Zn]23/C2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=C4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[PH](C5=CC=CC=C5)(C5=CC=CC=C5)[Zn]412)N3C.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=C5C6=C(/C=C\C7=C/6N(C6=C(C=CC=C6)N7)[PH](C6=CC=CC=C6)(C6=CC=CC=C6)[Zn]45N4C=N(C)C1=C24)O3.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)N(C4=CC=CC=C4)(C4=CC=CC=C4)[Zn]53N2=C1 WIFNMGMDQUMBOA-UHFFFAOYSA-Q 0.000 description 1
- HMUOKRNWQCSUGK-UHFFFAOYSA-N C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7C7=C(C=C8)C8=CC=CC=C8[Ag]72C3=C56)S4)C=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7C7=C(C=C8)C8=CC=CC=C8[Ag]72C3=C56)S4)C=C1 HMUOKRNWQCSUGK-UHFFFAOYSA-N 0.000 description 1
- HSJFNFKTDABSAM-UHFFFAOYSA-N C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7C7=C(C=C8)C8=CC=CC=C8[Au]72C3=C56)S4)C=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7C7=C(C=C8)C8=CC=CC=C8[Au]72C3=C56)S4)C=C1 HSJFNFKTDABSAM-UHFFFAOYSA-N 0.000 description 1
- KQMWOZXFDWLCSU-UHFFFAOYSA-N C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7C7=C(C=C8)C8=CC=CC=C8[Cu]72C3=C56)S4)C=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C5C6=C(C=CC=C6)N6C7=COC8=C7C7=C(C=C8)C8=CC=CC=C8[Cu]72C3=C56)S4)C=C1 KQMWOZXFDWLCSU-UHFFFAOYSA-N 0.000 description 1
- KXPYZYCPSPGQDH-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3\C3=C(\C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Ag]2(\C3=C/54)/C2=C/C=C/C=C\72)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Ag]23C2=CC=CC=C2C2=N3C3=C(C=C2)/C=C\C=C\43)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(/C=C3/C=C\4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Ag]52C2=CC=CC3=C2C4=CC=C3)C=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3\C3=C(\C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Ag]2(\C3=C/54)/C2=C/C=C/C=C\72)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Ag]23C2=CC=CC=C2C2=N3C3=C(C=C2)/C=C\C=C\43)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(/C=C3/C=C\4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Ag]52C2=CC=CC3=C2C4=CC=C3)C=C1 KXPYZYCPSPGQDH-UHFFFAOYSA-O 0.000 description 1
- SFACEMBJFCSAMX-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3\C3=C(\C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Au]2(\C3=C/54)/C2=C/C=C/C=C\72)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Au]23C2=CC=CC=C2C2=N3C3=C(C=C2)/C=C\C=C\43)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(/C=C3/C=C\4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Au]52C2=CC=CC3=C2C4=CC=C3)C=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3\C3=C(\C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Au]2(\C3=C/54)/C2=C/C=C/C=C\72)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Au]23C2=CC=CC=C2C2=N3C3=C(C=C2)/C=C\C=C\43)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(/C=C3/C=C\4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Au]52C2=CC=CC3=C2C4=CC=C3)C=C1 SFACEMBJFCSAMX-UHFFFAOYSA-O 0.000 description 1
- DHZOGHLRBCQIPC-UHFFFAOYSA-O C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3\C3=C(\C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Cu]2(\C3=C/54)/C2=C/C=C/C=C\72)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Cu]23C2=CC=CC=C2C2=N3C3=C(C=C2)/C=C\C=C\43)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(/C=C3/C=C\4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Cu]52C2=CC=CC3=C2C4=CC=C3)C=C1 Chemical compound C1=CC=C([PH]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3\C3=C(\C=C/4)N4C5=C(C=CC=C5)N5C6=CC=CC7=N6[Cu]2(\C3=C/54)/C2=C/C=C/C=C\72)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)C3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Cu]23C2=CC=CC=C2C2=N3C3=C(C=C2)/C=C\C=C\43)C=C1.C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=N5C6=C(/C=C3/C=C\4)C3=C(C=CC=C3)N6C3=CC=CC4=C3[Cu]52C2=CC=CC3=C2C4=CC=C3)C=C1 DHZOGHLRBCQIPC-UHFFFAOYSA-O 0.000 description 1
- JFDMGLNFGDPCQD-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Mn]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Mn]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Mn]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Mn]53C2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Mn]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Mn]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Mn]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Mn]53C2=C1 JFDMGLNFGDPCQD-UHFFFAOYSA-N 0.000 description 1
- XSVMLMUKNPPHPM-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Ni]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Ni]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Ni]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ni]53C2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Ni]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Ni]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Ni]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ni]53C2=C1 XSVMLMUKNPPHPM-UHFFFAOYSA-N 0.000 description 1
- ATOJGUJPGVRHSI-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Pd]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Pd]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Pd]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Pd]53C2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Pd]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Pd]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Pd]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Pd]53C2=C1 ATOJGUJPGVRHSI-UHFFFAOYSA-N 0.000 description 1
- SMEFYNGDIYXYMO-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Pt]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Pt]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Pt]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Pt]53C2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Pt]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Pt]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Pt]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Pt]53C2=C1 SMEFYNGDIYXYMO-UHFFFAOYSA-N 0.000 description 1
- XWTMNJCIBCJVKA-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Zn]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Zn]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Zn]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Zn]53C2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)C3=CC=CC4=C3N3=C(O4)N4C5=C(C=CC=C5)OC5=C/C6=CC=CC7=C6\N(=C/54)[Zn]32N2=CC=CC=C72)C=C1.CC1=CC(C)=C2N1C1=COC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Zn]214)N3C.CN1C2=CC3=C4C(=CC=C3)/C3=C(/OC5=C3C=CC=C5)[Zn]35C6=CC=CC=C6C6=COC7=C6/N3=C(\O7)N(C3=C1C=CC=C3)C2=N45.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)OC4=C6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Zn]53C2=C1 XWTMNJCIBCJVKA-UHFFFAOYSA-N 0.000 description 1
- GYPKCNXXGFERGG-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Mn]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Mn]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Mn]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Mn]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)N2=CN(C)C3=C/C=C/C1=C\32 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Mn]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Mn]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Mn]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Mn]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)N2=CN(C)C3=C/C=C/C1=C\32 GYPKCNXXGFERGG-UHFFFAOYSA-N 0.000 description 1
- OOBSJXHFIRLROW-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Ni]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Ni]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Ni]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Ni]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)C2=CN(C)/C3=C/C=C/C1=C\23 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Ni]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Ni]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Ni]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Ni]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)C2=CN(C)/C3=C/C=C/C1=C\23 OOBSJXHFIRLROW-UHFFFAOYSA-N 0.000 description 1
- FAJDDJBHTVGSCF-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Pd]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Pd]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Pd]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Pd]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)C2=CN(C)/C3=C/C=C/C1=C\23 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Pd]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Pd]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Pd]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Pd]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)C2=CN(C)/C3=C/C=C/C1=C\23 FAJDDJBHTVGSCF-UHFFFAOYSA-N 0.000 description 1
- ZZYDXEVFYGSZBC-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Pt]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Pt]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Pt]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Pt]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)N2=CN(C)C3=C/C=C/C1=C\32 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Pt]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Pt]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Pt]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Pt]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)N2=CN(C)C3=C/C=C/C1=C\32 ZZYDXEVFYGSZBC-UHFFFAOYSA-N 0.000 description 1
- FPWVFFUZIVHROR-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Zn]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Zn]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Zn]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Zn]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)N2=CN(C)C3=C/C=C/C1=C\32 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3/N3=C5/N(C6=CC=CC7=N6[Zn]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=N3[Zn]23C2=C(C=CC=C2)C2=N3C3=C(C=C2)CCC2=C(C=CC=C2)N31.C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1/N1=C5C(=C/4)\C4=C(C=CC=C4)N\5N4C(=CC5=C4C=CC=C5)[Zn]231.CN1C2=C(C=CC=C2)N2C3=C1C=CC1=N3[Zn]3(C4=CC=CC=C4C4=C5C(=CC=C4)N(C)/C2=N\53)N2=CN(C)C3=C/C=C/C1=C\32 FPWVFFUZIVHROR-UHFFFAOYSA-N 0.000 description 1
- XXHCGURDICOCRM-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Ag]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Ag]214)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC7=C6C(C)(C6=C(C=CC=C6)C7(C)C)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Ag]53C2=C1)O4 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Ag]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Ag]214)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC7=C6C(C)(C6=C(C=CC=C6)C7(C)C)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Ag]53C2=C1)O4 XXHCGURDICOCRM-UHFFFAOYSA-N 0.000 description 1
- VQJBGMWNZBTQCT-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Au]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Au]214)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC7=C6C(C)(C6=C(C=CC=C6)C7(C)C)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Au]53C2=C1)O4 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Au]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Au]214)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC7=C6C(C)(C6=C(C=CC=C6)C7(C)C)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Au]53C2=C1)O4 VQJBGMWNZBTQCT-UHFFFAOYSA-N 0.000 description 1
- OCJIIRMNIPLFKK-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Cu]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]214)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC7=C6C(C)(C6=C(C=CC=C6)C7(C)C)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]53C2=C1)O4 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=C3[Cu]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N43)C=C1.CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]214)N3C.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC7=C6C(C)(C6=C(C=CC=C6)C7(C)C)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]53C2=C1)O4 OCJIIRMNIPLFKK-UHFFFAOYSA-N 0.000 description 1
- REWVCRKMAIPCHI-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Co]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Co]421)N3C.CN1C=C2C3=C1N(C)=CN3[Co]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C4=C/1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Co]53N2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Co]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Co]421)N3C.CN1C=C2C3=C1N(C)=CN3[Co]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C4=C/1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Co]53N2=C1 REWVCRKMAIPCHI-UHFFFAOYSA-N 0.000 description 1
- XVPOOUKDEJHPKT-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Cu]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]421)N3C.CN1C=C2C3=C1N(C)=CN3[Cu]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C4=C/1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]53N2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Cu]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Cu]421)N3C.CN1C=C2C3=C1N(C)=CN3[Cu]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C4=C/1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]53N2=C1 XVPOOUKDEJHPKT-UHFFFAOYSA-N 0.000 description 1
- DTIOUIZJYYFACD-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Ir]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Ir]421)N3C.CN1C=C2C3=C1N(C)=CN3[Ir]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C4=C/1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]53N2=C1 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Ir]23/N2=C(/C=C\C5=C2N4C2=C5C=CC=C2)C2=CC=CC4=C2/N3=C\O4)C=C1.CC1=CC(C)=N2N1C1=COC3=C1/N1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(/C=C\C6=C/5N(C5=C6C=CC=C5)[Si](C5=CC=CC=C5)(C5=CC=CC=C5)[Ir]421)N3C.CN1C=C2C3=C1N(C)=CN3[Ir]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(/C=C\C4=C/1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C6=C(O4)O/C4=C\6C(C)(C6=C(C=CC=C6)C4(C)C)[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]53N2=C1 DTIOUIZJYYFACD-UHFFFAOYSA-N 0.000 description 1
- WIRMDPPWPMWFNV-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Mn]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Mn]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Mn]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Mn]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 WIRMDPPWPMWFNV-UHFFFAOYSA-N 0.000 description 1
- MACMRMIHIUAFBW-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Ni]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\N3[Ni]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Ni]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\N3[Ni]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 MACMRMIHIUAFBW-UHFFFAOYSA-N 0.000 description 1
- MAJSTIPQSWSLPU-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Pd]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\N3[Pd]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Pd]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\N3[Pd]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 MAJSTIPQSWSLPU-UHFFFAOYSA-N 0.000 description 1
- GLJBOPDANKCGRX-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Pt]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\N3[Pt]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Pt]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\N3[Pt]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 GLJBOPDANKCGRX-UHFFFAOYSA-N 0.000 description 1
- WNWXSHGXGAOOQY-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Zn]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Zn]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C(C=C4)OC4=N3[Zn]23C2=COC5=C2C(=CC=C5)C2=N3C3=C(C=C2)C2=C(C=CC=C2)N34)C=C1.CN1C=C2C3=C1/N(C)=C\C3[Zn]13N4=C2C=CC2=C4N(C4=C(C=CC=C4)N2C)C2=N1C1=C(C=CC4=C1N(C1=C(C=CC=C1)N4)[Si]3(C1=CC=CC=C1)C1=CC=CC=C1)O2 WNWXSHGXGAOOQY-UHFFFAOYSA-N 0.000 description 1
- ZESLIEBGZMYBAU-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5N(C6=CC=CC7=N6[Ag]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)C=CC1=C3[Ag]23C2=C(C=CC=C2)C2=N\3C3=C(\C=C/2)CCC2=C(C=CC=C2)N13.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C(=CC5=C4C=CC=C5)[Ag]231 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5N(C6=CC=CC7=N6[Ag]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)C=CC1=C3[Ag]23C2=C(C=CC=C2)C2=N\3C3=C(\C=C/2)CCC2=C(C=CC=C2)N13.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C(=CC5=C4C=CC=C5)[Ag]231 ZESLIEBGZMYBAU-UHFFFAOYSA-N 0.000 description 1
- UVMUAKXUTFYRMP-UHFFFAOYSA-N C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5N(C6=CC=CC7=N6[Cu]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)C=CC1=C3[Cu]23C2=C(C=CC=C2)C2=N\3C3=C(\C=C/2)CCC2=C(C=CC=C2)N13.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C(=CC5=C4C=CC=C5)[Cu]231 Chemical compound C1=CC=C([Si]2(C3=CC=CC=C3)N3C4=C(C=CC=C4)C4=C3C3=C5N(C6=CC=CC7=N6[Cu]32C2=CC=CN27)C2=C(C=CC=C2)N45)C=C1.C1=CC=C2C(=C1)C1=C3C(=CC=C1)C=CC1=C3[Cu]23C2=C(C=CC=C2)C2=N\3C3=C(\C=C/2)CCC2=C(C=CC=C2)N13.C1=CC=C2C(=C1)C1=C3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1N1=C5C(=C4)C4=C(C=CC=C4)N5N4C(=CC5=C4C=CC=C5)[Cu]231 UVMUAKXUTFYRMP-UHFFFAOYSA-N 0.000 description 1
- YZYHDBBZVPTQRL-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ag]26/C3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Ag]243.CC1=CC(C)=C2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ag]324 Chemical compound C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Ag]26/C3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Ag]243.CC1=CC(C)=C2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Ag]324 YZYHDBBZVPTQRL-UHFFFAOYSA-N 0.000 description 1
- FXRUOZXWYZQAOD-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Au]26/C3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Au]243.CC1=CC(C)=C2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Au]324 Chemical compound C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Au]26/C3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Au]243.CC1=CC(C)=C2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Au]324 FXRUOZXWYZQAOD-UHFFFAOYSA-N 0.000 description 1
- TXPHOBWKCUWDME-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Cu]26/C3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Cu]243.CC1=CC(C)=C2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Cu]324 Chemical compound C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C1OC4=C(C=CC=C4)N4C5=N6C(=CC=C5)C5=C(C=CC=C5)[Cu]26/C3=C/14.C1=CC=C2C(=C1)C1=N3C4=C(C=C1)C1=C(C=CC=C1)N4C1=C4/C5=C(\C=C/1)C1=C(C=CC=C1)C5C1=C(SC5=C1C=CC=C5)[Cu]243.CC1=CC(C)=C2N1C1=C3C4=C(C=C1)C1=C(C=CC=C1)N4C1=N4/C5=C(\C=C/1)C1=C(C=CC=C1)N5C1=C(C=CC=C1)[Cu]324 TXPHOBWKCUWDME-UHFFFAOYSA-N 0.000 description 1
- WPLTZCCJFWBTJH-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Au]23C2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.CN1C=C2C3=C(C=CC=C31)C1=C3C4=C(C=C1)N(C)C1=C(C=CC=C1)N4C1=N4C5=C(C=CC=C5N1C)C1=CC=CC=C1[Au]234.CN1C=CC2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Au]213 Chemical compound C1=CC=C2C(=C1)C1=C3C(=CC=C1)/C=C\C1=C/3[Au]23C2=C(C=CC=C2)C2=N3C3=C(/C=C\2)CCC2=C(C=CC=C2)N31.CN1C=C2C3=C(C=CC=C31)C1=C3C4=C(C=C1)N(C)C1=C(C=CC=C1)N4C1=N4C5=C(C=CC=C5N1C)C1=CC=CC=C1[Au]234.CN1C=CC2=C1N1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C(C=C4)N4C5=C(C=CC=C5)C5=C4C(=CC=C5)[Au]213 WPLTZCCJFWBTJH-UHFFFAOYSA-N 0.000 description 1
- NMCFCOKQBGLXGI-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C/C=C6C(=C/51)\C4(C1=C(C=C4[U]C5=C(C=CC=C5)C4=C1)N23)C1CCCC\61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C4(C1=C(C4=C(C=C1)C1=C(C=CC=C1)[U]4)N23)C1CCCC/61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C4(C1=C(C4=C(C=C1)[U]C1=C4C=CC=C1)N23)C1CCCC/61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C4(C1=C(C=C4C(=C1)[U]C1=C4C=CC=C1)N23)C1CCCC/61 Chemical compound C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C/C=C6C(=C/51)\C4(C1=C(C=C4[U]C5=C(C=CC=C5)C4=C1)N23)C1CCCC\61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C4(C1=C(C4=C(C=C1)C1=C(C=CC=C1)[U]4)N23)C1CCCC/61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C4(C1=C(C4=C(C=C1)[U]C1=C4C=CC=C1)N23)C1CCCC/61.C1=CC=C2C(=C1)C1=C3C4=C(C=C1)N1C5=C(C=CC=C5)C5=C\C=C6C(=C/51)/C4(C1=C(C=C4C(=C1)[U]C1=C4C=CC=C1)N23)C1CCCC/61 NMCFCOKQBGLXGI-UHFFFAOYSA-N 0.000 description 1
- CYVGPSRLARFEJU-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C/C5=C(\C=N/1C41C4=C(C=CC=C4C4CCCC41)N23)C1=C(C=CC=C1)[U]5.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5\C6=C(C=CC=C6)[U]\C5=C\C=N\1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5\[U]C6=C(C=CC=C6)\C5=C\C=N\1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=N1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)[U]C1=C2/C=C2/N3C4=C(C=CC=C4)C4=CC5=C6C(=C43)C3(C4=C(C=CC=C4C4CCCC43)N6C3=CC=CC=C35)/N2=C/1 Chemical compound C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C/C5=C(\C=N/1C41C4=C(C=CC=C4C4CCCC41)N23)C1=C(C=CC=C1)[U]5.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5\C6=C(C=CC=C6)[U]\C5=C\C=N\1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5\[U]C6=C(C=CC=C6)\C5=C\C=N\1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC=CC=N1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)[U]C1=C2/C=C2/N3C4=C(C=CC=C4)C4=CC5=C6C(=C43)C3(C4=C(C=CC=C4C4CCCC43)N6C3=CC=CC=C35)/N2=C/1 CYVGPSRLARFEJU-UHFFFAOYSA-N 0.000 description 1
- GXVOTSPRXCVLSA-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5C(=CC(=C1)C41C4=C(C=CC=C4C4CCCC41)N23)[U]C1=C5C=CC=C1.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5[U]C6=C(C=CC=C6)C5=CC=C1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC5=C(C(=C1)C41C4=C(C=CC=C4C4CCCC41)N23)C1=C(C=CC=C1)[U]5.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC5=C([U]C6=C5C=CC=C6)C(=C1)C41C4=C(C=CC=C4C4CCCC41)N23.CC.CC.CC.CC Chemical compound C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5C(=CC(=C1)C41C4=C(C=CC=C4C4CCCC41)N23)[U]C1=C5C=CC=C1.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=C5[U]C6=C(C=CC=C6)C5=CC=C1C41C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC5=C(C(=C1)C41C4=C(C=CC=C4C4CCCC41)N23)C1=C(C=CC=C1)[U]5.C1=CC=C2C(=C1)C1=C3C4=C5C(=C1)C1=C(C=CC=C1)N5C1=CC5=C([U]C6=C5C=CC=C6)C(=C1)C41C4=C(C=CC=C4C4CCCC41)N23.CC.CC.CC.CC GXVOTSPRXCVLSA-UHFFFAOYSA-N 0.000 description 1
- XJSUYIPXRWUFPI-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=C3N2C2=C4C(=CC=C2)C2CCCC2C42N3=C3C(=C1)C1=C(C=CC=C1)N3C1=C/C3=C(\C=N/12)C1=C(C=CC=C1)[U]3.C1=CC=C2C(=C1)C1=C3N2C2=C4C(=CC=C2)C2CCCC2C42N3=C3C(=C1)C1=C(C=CC=C1)N3C1=C3\[U]C4=C(C=CC=C4)\C3=C\C=N\12.C1=CC=C2C(=C1)C1=C3N2C2=C4C(=CC=C2)C2CCCC2C42N4=CC=CC=C4N4C5=C(C=CC=C5)C(=C1)C4=N32.C1=CC=C2C(=C1)C1=C3N=C4C(=C1)C1=C(C=CC=C1)N4C1=C4\C5=C(C=CC=C5)[U]\C4=C\C=N\1C1C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)[U]C1=C2/C=C2/N3C4=C(C=CC=C4)C4=CC5=C6N(C7=CC=CC=C75)C5=C7C(=CC=C5)C5CCCC5C7(N6=C43)/N2=C/1 Chemical compound C1=CC=C2C(=C1)C1=C3N2C2=C4C(=CC=C2)C2CCCC2C42N3=C3C(=C1)C1=C(C=CC=C1)N3C1=C/C3=C(\C=N/12)C1=C(C=CC=C1)[U]3.C1=CC=C2C(=C1)C1=C3N2C2=C4C(=CC=C2)C2CCCC2C42N3=C3C(=C1)C1=C(C=CC=C1)N3C1=C3\[U]C4=C(C=CC=C4)\C3=C\C=N\12.C1=CC=C2C(=C1)C1=C3N2C2=C4C(=CC=C2)C2CCCC2C42N4=CC=CC=C4N4C5=C(C=CC=C5)C(=C1)C4=N32.C1=CC=C2C(=C1)C1=C3N=C4C(=C1)C1=C(C=CC=C1)N4C1=C4\C5=C(C=CC=C5)[U]\C4=C\C=N\1C1C4=C(C=CC=C4C4CCCC41)N23.C1=CC=C2C(=C1)[U]C1=C2/C=C2/N3C4=C(C=CC=C4)C4=CC5=C6N(C7=CC=CC=C75)C5=C7C(=CC=C5)C5CCCC5C7(N6=C43)/N2=C/1 XJSUYIPXRWUFPI-UHFFFAOYSA-N 0.000 description 1
- ORPFYDZPOQBAPL-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C(C=C4)C4=C(C=CC=C4)[Ag]213.CN1C2=C(C=CC=C2)C2=C1[Ag]13C4=CC=CN4C4=C1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Au]45C4=CN(C)C1=C24)O3 Chemical compound C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C(C=C4)C4=C(C=CC=C4)[Ag]213.CN1C2=C(C=CC=C2)C2=C1[Ag]13C4=CC=CN4C4=C1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Au]45C4=CN(C)C1=C24)O3 ORPFYDZPOQBAPL-UHFFFAOYSA-N 0.000 description 1
- VIAHLTAHAHNRID-UHFFFAOYSA-N C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C(C=C4)C4=C(C=CC=C4)[Cu]213.CN1C2=C(C=CC=C2)C2=C1[Cu]13C4=CC=CN4C4=C1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Ag]45C4=CN(C)C1=C24)O3 Chemical compound C1=CC=C2C(=C1)C1=N3C(=CC=C1)N1C4=C(C=CC=C4)C4=C1C1=C(C=C4)C4=C(C=CC=C4)[Cu]213.CN1C2=C(C=CC=C2)C2=C1[Cu]13C4=CC=CN4C4=C1C(=CC=C4)N1C=CC4=C1/N3=C/2O4.CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Ag]45C4=CN(C)C1=C24)O3 VIAHLTAHAHNRID-UHFFFAOYSA-N 0.000 description 1
- FJUWTTDYFTWJLY-UHFFFAOYSA-N CC(C1C)C1N Chemical compound CC(C1C)C1N FJUWTTDYFTWJLY-UHFFFAOYSA-N 0.000 description 1
- CKVXXHAUIBUYEE-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Ag]2(C4=C(C=CC5=C4N3C3=C(C=CC=C3)CC5)C3=CC=CC4=C3/C2=C\C=C/4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=C2N1C1=CSC3=C1/C1=C(\S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ag]421.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Ag]342.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4C(=CS6)[Ag]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Ag]2(C4=C(C=CC5=C4N3C3=C(C=CC=C3)CC5)C3=CC=CC4=C3/C2=C\C=C/4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=C2N1C1=CSC3=C1/C1=C(\S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ag]421.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Ag]342.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4C(=CS6)[Ag]53N2=C1 CKVXXHAUIBUYEE-UHFFFAOYSA-O 0.000 description 1
- GUJUKYIRANDUEH-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Au]2(C4=C(C=CC5=C4N3C3=C(C=CC=C3)CC5)C3=CC=CC4=C3/C2=C\C=C/4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=C2N1C1=CSC3=C1/C1=C(\S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Au]421.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Au]342.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4C(=CS6)[Au]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Au]2(C4=C(C=CC5=C4N3C3=C(C=CC=C3)CC5)C3=CC=CC4=C3/C2=C\C=C/4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=C2N1C1=CSC3=C1/C1=C(\S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5C(=CC=C3)[Au]421.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Au]342.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4C(=CS6)[Au]53N2=C1 GUJUKYIRANDUEH-UHFFFAOYSA-O 0.000 description 1
- HFQRVGYHOMILAD-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Cu]2(C4=C(C=CC5=C4N3C3=C(C=CC=C3)CC5)C3=CC=CC4=C3/C2=C\C=C/4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=C2N1C1=CSC3=C1/C1=C(\S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Cu]421.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Cu]342.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4C(=CS6)[Cu]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Cu]2(C4=C(C=CC5=C4N3C3=C(C=CC=C3)CC5)C3=CC=CC4=C3/C2=C\C=C/4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=C2N1C1=CSC3=C1/C1=C(\S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Cu]421.CN1=CN2C3=C1/C=C\C=C/3C1=C3C4=C(C=C1)CCC1=C(C=CC=C1)N4C1=C4C(=CC=C1)N1C5=C(C=CC=C5)C5=C1C(=CC=C5)[Cu]342.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4C(=CS6)[Cu]53N2=C1 HFQRVGYHOMILAD-UHFFFAOYSA-O 0.000 description 1
- CSSWUPRGTIGNAI-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Mn]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Mn]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Mn]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Mn]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Mn]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Mn]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Mn]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Mn]53N2=C1 CSSWUPRGTIGNAI-UHFFFAOYSA-O 0.000 description 1
- VHRIXWYORCAURB-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Ni]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ni]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Ni]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ni]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Ni]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ni]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Ni]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ni]53N2=C1 VHRIXWYORCAURB-UHFFFAOYSA-O 0.000 description 1
- HVJGVCWICNINJO-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Pd]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Pd]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Pd]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Pd]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Pd]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Pd]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Pd]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Pd]53N2=C1 HVJGVCWICNINJO-UHFFFAOYSA-O 0.000 description 1
- NNAPPPUPQSDTBB-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Pt]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Pt]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Pt]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Pt]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Pt]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Pt]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Pt]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Pt]53N2=C1 NNAPPPUPQSDTBB-UHFFFAOYSA-O 0.000 description 1
- APVUBIRYTRGLTQ-UHFFFAOYSA-O CC1(C)C2=CC=CC3=C2[Zn]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Zn]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Zn]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Zn]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=C2[Zn]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)CCC3=C5N(=CC=C3)[Zn]412.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=C4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Zn]412.CN1C=C2C3=CSC4=C3/C3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Zn]53N2=C1 APVUBIRYTRGLTQ-UHFFFAOYSA-O 0.000 description 1
- BHFGRSYMBLUXDA-UHFFFAOYSA-O CC1(C)C2=CC=CC3=N2[Co]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Co]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Co]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Co]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=N2[Co]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Co]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Co]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Co]53N2=C1 BHFGRSYMBLUXDA-UHFFFAOYSA-O 0.000 description 1
- BLIDDNIOBOPYGC-UHFFFAOYSA-O CC1(C)C2=CC=CC3=N2[Cu]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Cu]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Cu]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Cu]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=N2[Cu]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Cu]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Cu]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Cu]53N2=C1 BLIDDNIOBOPYGC-UHFFFAOYSA-O 0.000 description 1
- JQZQXKWQTPNJHX-UHFFFAOYSA-O CC1(C)C2=CC=CC3=N2[Ir]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ir]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Ir]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ir]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=N2[Ir]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Ir]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Ir]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Ir]53N2=C1 JQZQXKWQTPNJHX-UHFFFAOYSA-O 0.000 description 1
- SXUVQUBFOREPFV-UHFFFAOYSA-O CC1(C)C2=CC=CC3=N2[Rh]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Rh]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Rh]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Rh]53N2=C1 Chemical compound CC1(C)C2=CC=CC3=N2[Rh]2(/C4=C(/C=C\C5=C4N3C3=C(C=CC=C3)CC5)C3=C\C=C/C4=C/3N2=CC=C4)[PH]1(C1=CC=CC=C1)C1=CC=CC=C1.CC1=CC(C)=N2N1C1=CSC3=C1C1=C(S3)N(C3=CC=CC=C3)C3=N4C5=C(C=C3)CCC3=C5N(=CC=C3)[Rh]142.CN1C2=C(C=CC=C2)N2=C1C1=CC=CC3=C1C1=C(O3)N(C3=CC=CC=C3)C3=N4C(=CC=C3)C3=CSC5=C3N(=CC=C5)[Rh]124.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5C4=C5C(=CC=C4)C4=CSC6=C4N(=CS6)[Rh]53N2=C1 SXUVQUBFOREPFV-UHFFFAOYSA-O 0.000 description 1
- ANPZBQGSFVSFKL-UHFFFAOYSA-N CC1=C(C2=CC(OC3=CC4=C(C=C3)C3=C(C=CC=C3)N4C3=NC=CC=C3)=CC=C2)N=CC=C1C1=CC=C(C2=CC=CC=C2)C=C1.CC1=C2C3=C4C(=CC=C3)OC3=C5C6=C(C=C3)C3=C(C=CC=C3)N6C3=N(C=CC=C3)[Pd]54N2=CC=C1C1=CC=C(C2=CC=CC=C2)C=C1 Chemical compound CC1=C(C2=CC(OC3=CC4=C(C=C3)C3=C(C=CC=C3)N4C3=NC=CC=C3)=CC=C2)N=CC=C1C1=CC=C(C2=CC=CC=C2)C=C1.CC1=C2C3=C4C(=CC=C3)OC3=C5C6=C(C=C3)C3=C(C=CC=C3)N6C3=N(C=CC=C3)[Pd]54N2=CC=C1C1=CC=C(C2=CC=CC=C2)C=C1 ANPZBQGSFVSFKL-UHFFFAOYSA-N 0.000 description 1
- PPAOHKYHVQIXBA-XRNJTEMRSA-N CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CC1CCCC1C.CN/C(C)=C\C=C/[U] Chemical compound CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CC1CCCC1C.CN/C(C)=C\C=C/[U] PPAOHKYHVQIXBA-XRNJTEMRSA-N 0.000 description 1
- OWBGNBDMONJKCZ-DGGMBMFWSA-N CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CN/C(C)=C\C=C/[U] Chemical compound CC1=C2/C=C\C=C/C2=CC=N1C.CC1=C2/C=C\C=C/C2=[U]C=N1C.CC1=C2C(=CC=N1C)[U]C1=C2C=CC=C1.CC1=CC2=C(C=CC=C2)C=N1C.CC1=CC2=C(C=N1C)C1=C(C=CC=C1)[U]2.CC1=CC2=C(C=N1C)[U]C1=C2C=CC=C1.CC1=CC=C2C3=C(C=CC=C3)[U]C2=N1C.CC1=CC=C2C=CC=CC2=N1C.CC1=CC=C2[U]C3=C(C=CC=C3)C2=N1C.CC1=CC=CC=N1C.CC1=CC=[U]C=N1C.CC1=C[U]=C2C=CC=CC2=N1C.CC1=C[U]=CC=N1C.CC1=[U]C2=C(C=CC=C2)C=N1C.CN/C(C)=C\C=C/[U] OWBGNBDMONJKCZ-DGGMBMFWSA-N 0.000 description 1
- DDWCHLSCQRFIAM-YUHOEWHHSA-N CC1=CC(/C=C/C2=CC=CC=C2)=CC(C)=C1C.CC1=CC(C2=CC=C3C(=C2)[U]C2=C3C=CC=C2)=CC(C)=C1C.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C.CC1=CC=C(/C=C/C2=CC=CC=C2)C=C1.CC1=CC=C(C2=CC=CC=C2)C=C1.CC1=CC=C2C(=C1)[U]C1=C2C=CC=C1 Chemical compound CC1=CC(/C=C/C2=CC=CC=C2)=CC(C)=C1C.CC1=CC(C2=CC=C3C(=C2)[U]C2=C3C=CC=C2)=CC(C)=C1C.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C.CC1=CC=C(/C=C/C2=CC=CC=C2)C=C1.CC1=CC=C(C2=CC=CC=C2)C=C1.CC1=CC=C2C(=C1)[U]C1=C2C=CC=C1 DDWCHLSCQRFIAM-YUHOEWHHSA-N 0.000 description 1
- VULPVJIDNNPPFQ-RRABGKBLSA-N CC1=CC(/C=C/C2=CC=CC=C2)=CC(C)=C1C.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C Chemical compound CC1=CC(/C=C/C2=CC=CC=C2)=CC(C)=C1C.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C VULPVJIDNNPPFQ-RRABGKBLSA-N 0.000 description 1
- WETKIKYBKIKEPU-UHFFFAOYSA-N CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5C5=C(/C=C/C=C/5CC6)[Ag]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Ag]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC=C6C6=C(C=CC=C6)[Ag]53C2=C1)O4 Chemical compound CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5C5=C(/C=C/C=C/5CC6)[Ag]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Ag]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC=C6C6=C(C=CC=C6)[Ag]53C2=C1)O4 WETKIKYBKIKEPU-UHFFFAOYSA-N 0.000 description 1
- BRYJFJKRMVDQBR-UHFFFAOYSA-N CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5C5=C(/C=C/C=C/5CC6)[Au]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Au]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC=C6C6=C(C=CC=C6)[Au]53C2=C1)O4 Chemical compound CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5C5=C(/C=C/C=C/5CC6)[Au]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Au]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC=C6C6=C(C=CC=C6)[Au]53C2=C1)O4 BRYJFJKRMVDQBR-UHFFFAOYSA-N 0.000 description 1
- FVMJANKRTZKNOI-UHFFFAOYSA-N CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5C5=C(/C=C/C=C/5CC6)[Cu]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Cu]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC=C6C6=C(C=CC=C6)[Cu]53C2=C1)O4 Chemical compound CC1=CC(C)=C2N1C1=COC3=C1/C1=C(\O3)N(C3=CC=CC=C3)C3=N4C5=C(C=CC6=C5C5=C(/C=C/C=C/5CC6)[Cu]214)N3C.CN1C2=C(C=CC=C2)C2=C1C1=CC=CC3=C1N1=C(O3)N(C3=CC=CC=C3)C3=C4C5=C(C=C3)O/C=C\5C3=C(C=C5C=CC=CC5=C3)[Cu]241.CN1C=C2C3=CSC4=C3/N3=C5C(=C/4)\C4=C(C=CC=C4)N\5/C4=C5/C6=C(OC=C6C6=C(C=CC=C6)[Cu]53C2=C1)O4 FVMJANKRTZKNOI-UHFFFAOYSA-N 0.000 description 1
- APPQGIPYYJTFIN-UHFFFAOYSA-N CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC(C2=CC=CC=N2)=CC(OC2=CC3=C(C=C2)C2=C(C=CC=C2)N3C2=NC=CC=C2)=C1.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC2=C3C(=C1)OC1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pd]43N1=CC=CC=C21 Chemical compound CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC(C2=CC=CC=N2)=CC(OC2=CC3=C(C=C2)C2=C(C=CC=C2)N3C2=NC=CC=C2)=C1.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC2=C3C(=C1)OC1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pd]43N1=CC=CC=C21 APPQGIPYYJTFIN-UHFFFAOYSA-N 0.000 description 1
- WXDVRKJBHDOGEV-UHFFFAOYSA-N CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC=N2C(=C1)C1=C3C(=CC=C1)OC1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pd]432.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC=NC(C2=CC(OC3=CC4=C(C=C3)C3=C(C=CC=C3)N4C3=NC=CC=C3)=CC=C2)=C1 Chemical compound CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC=N2C(=C1)C1=C3C(=CC=C1)OC1=C4C5=C(C=C1)C1=C(C=CC=C1)N5C1=N(C=CC=C1)[Pd]432.CC1=CC(C2=CC=CC=C2)=CC(C)=C1C1=CC=NC(C2=CC(OC3=CC4=C(C=C3)C3=C(C=CC=C3)N4C3=NC=CC=C3)=CC=C2)=C1 WXDVRKJBHDOGEV-UHFFFAOYSA-N 0.000 description 1
- QCHAJUPIXZRQFZ-UHFFFAOYSA-N CC1=N[Co]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Co]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Co]\321.CN1CCN2C3=C1N1C4=N3[Co]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=N[Co]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Co]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Co]\321.CN1CCN2C3=C1N1C4=N3[Co]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 QCHAJUPIXZRQFZ-UHFFFAOYSA-N 0.000 description 1
- HKFUFKABXDDFTM-UHFFFAOYSA-N CC1=N[Cu]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Cu]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]\321.CN1CCN2C3=C1N1C4=N3[Cu]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=N[Cu]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Cu]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]\321.CN1CCN2C3=C1N1C4=N3[Cu]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 HKFUFKABXDDFTM-UHFFFAOYSA-N 0.000 description 1
- ZLWYUJGNBGVUIZ-UHFFFAOYSA-N CC1=N[Ir]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Ir]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]\321.CN1CCN2C3=C1N1C4=N3[Ir]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=N[Ir]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Ir]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]\321.CN1CCN2C3=C1N1C4=N3[Ir]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 ZLWYUJGNBGVUIZ-UHFFFAOYSA-N 0.000 description 1
- NAFVQXWFWQNYGM-UHFFFAOYSA-N CC1=N[Rh]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Rh]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Rh]\321.CN1CCN2C3=C1N1C4=N3[Rh]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=N[Rh]23N4=CC=CC=C4C4=C5C(=C/C=C/4)/OC(=N/52)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Rh]231.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[Si](C4=CC=CC=C4)(C4=CC=CC=C4)[Rh]\321.CN1CCN2C3=C1N1C4=N3[Rh]3(C5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 NAFVQXWFWQNYGM-UHFFFAOYSA-N 0.000 description 1
- ORKVVTXUEJOOBG-UHFFFAOYSA-O CC1=[SH][Co]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Co]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Co]\321.CN1CCN2C3=C1N1C4=C3[Co]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Co]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Co]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Co]\321.CN1CCN2C3=C1N1C4=C3[Co]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 ORKVVTXUEJOOBG-UHFFFAOYSA-O 0.000 description 1
- NPYXQZNZPJBJIG-UHFFFAOYSA-O CC1=[SH][Cu]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Cu]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]\321.CN1CCN2C3=C1N1C4=C3[Cu]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Cu]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Cu]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Cu]\321.CN1CCN2C3=C1N1C4=C3[Cu]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 NPYXQZNZPJBJIG-UHFFFAOYSA-O 0.000 description 1
- GZJIHJCXEVVFQQ-UHFFFAOYSA-O CC1=[SH][Ir]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Ir]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]\321.CN1CCN2C3=C1N1C4=C3[Ir]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Ir]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Ir]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Ir]\321.CN1CCN2C3=C1N1C4=C3[Ir]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 GZJIHJCXEVVFQQ-UHFFFAOYSA-O 0.000 description 1
- TWBLCTDMSMYEKV-UHFFFAOYSA-O CC1=[SH][Ni]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Ni]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Ni]\321.CN1CCN2C3=C1N1C4=C3[Ni]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Ni]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Ni]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Ni]\321.CN1CCN2C3=C1N1C4=C3[Ni]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 TWBLCTDMSMYEKV-UHFFFAOYSA-O 0.000 description 1
- LWSZEKQKPCNZKR-UHFFFAOYSA-O CC1=[SH][Pd]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Pd]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Pd]\321.CN1CCN2C3=C1N1C4=C3[Pd]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Pd]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Pd]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Pd]\321.CN1CCN2C3=C1N1C4=C3[Pd]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 LWSZEKQKPCNZKR-UHFFFAOYSA-O 0.000 description 1
- CUMFDWKZKBNZAE-UHFFFAOYSA-O CC1=[SH][Pt]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Pt]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Pt]\321.CN1CCN2C3=C1N1C4=C3[Pt]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Pt]23C4=C5C(=CC6=C4N(C4=C6C=CC=C4)C4=C2C2=C(/C=C\C=C/2O4)C2=CC=CC=N23)CCCC15.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Pt]312.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Pt]\321.CN1CCN2C3=C1N1C4=C3[Pt]3(C5=C(C=CC6=CC=CC(=C65)C5=CC6=C(C=CC=C6)C=N53)N4CCN1C)N1=C2C=CC=C1 CUMFDWKZKBNZAE-UHFFFAOYSA-O 0.000 description 1
- IXRFFYPBHVKUOP-UHFFFAOYSA-O CC1=[SH][Rh]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Rh]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Rh]\321.CN1CCN2C3=C1N1C4=C3[Rh]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 Chemical compound CC1=[SH][Rh]23C4=C(O/C5=C/C=C\C(=C/45)C4=CC=CC=N42)N2C4=C(C=CC=C4)C4=C2N3=C2C(=C4)CCCC12.CN1C2=C(C=CC=C2)N2=C1P1C=CC3=C1/C1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3N3=C5C(=C4)C4=C(C=CC=C4)C5N4C5=C(C=CC=C5)C=N4[Rh]132.CN1C=CN2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4/C3=C3C5=C/4C4=C(C=CC=C4)N/5[PH](C4=CC=CC=C4)(C4=CC=CC=C4)[Rh]\321.CN1CCN2C3=C1N1C4=C3[Rh]3(N5=CC6=C(C=CC=C6)C=C5C5=C6C(=CC=C5)C=CC(=N63)N4CCN1C)N1=C2C=CC=C1 IXRFFYPBHVKUOP-UHFFFAOYSA-O 0.000 description 1
- GOJQSWIQMUHEFL-UHFFFAOYSA-N CC1=[Si](C)[Ag]23C4=CC=CC5=C4N(/C=C\5)C4=C2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2N3=C2/C(=C\4)OC3=C(C=CC=C3)N21.CN1C=C2C3=C1/N(C)=C\C3[Ag]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1/C=C\C3=C1\N1=C(/N3C)N3C4=C(/C=C\C=C/4)N4C5=C6/C(=C\43)[Ag]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound CC1=[Si](C)[Ag]23C4=CC=CC5=C4N(/C=C\5)C4=C2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2N3=C2/C(=C\4)OC3=C(C=CC=C3)N21.CN1C=C2C3=C1/N(C)=C\C3[Ag]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1/C=C\C3=C1\N1=C(/N3C)N3C4=C(/C=C\C=C/4)N4C5=C6/C(=C\43)[Ag]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 GOJQSWIQMUHEFL-UHFFFAOYSA-N 0.000 description 1
- HWTASQBRULOATJ-UHFFFAOYSA-N CC1=[Si](C)[Au]23C4=CC=CC5=C4N(/C=C\5)C4=C2/C(=C/C=C/4)N2C4=C(C=CC=C4)C4=C\2N3=C2\C(=C/4)OC3=C(C=CC=C3)N21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C(=CC5=C4C=CC=C5)[Au]321.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6/C(=C\43)[Au]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound CC1=[Si](C)[Au]23C4=CC=CC5=C4N(/C=C\5)C4=C2/C(=C/C=C/4)N2C4=C(C=CC=C4)C4=C\2N3=C2\C(=C/4)OC3=C(C=CC=C3)N21.CN1C2=C(C=CC=C2)C2=C1P1C=CC3=C1/N1=C(\C=C/3)N3C4=C(C=CC=C4)C4=C3C3=C5C(=C4)C4=C(C=CC=C4)C5N4C(=CC5=C4C=CC=C5)[Au]321.CN1C=CC2=C1N1C=CC3=C1N1=C(N3C)N3C4=C(C=CC=C4)N4C5=C6/C(=C\43)[Au]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 HWTASQBRULOATJ-UHFFFAOYSA-N 0.000 description 1
- HEFFZFSZEWLJNG-UHFFFAOYSA-N CC1=[Si](C)[Cu]23C4=CC=CC5=C4N(/C=C\5)C4=C2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2N3=C2/C(=C\4)OC3=C(C=CC=C3)N21.CN1C=C2C3=C1/N(C)=C\C3[Cu]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1/C=C\C3=C1\N1=C(/N3C)N3C4=C(/C=C\C=C/4)N4C5=C6/C(=C\43)[Cu]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 Chemical compound CC1=[Si](C)[Cu]23C4=CC=CC5=C4N(/C=C\5)C4=C2C(=CC=C4)N2C4=C(C=CC=C4)C4=C2N3=C2/C(=C\4)OC3=C(C=CC=C3)N21.CN1C=C2C3=C1/N(C)=C\C3[Cu]13C4=C(C=CC=C4)N4C5=C(C=CC=C5)N(C)C5=C4C1=C1N(CCN(C)N51)C1=CC=CC2=N13.CN1C=CC2=C1N1/C=C\C3=C1\N1=C(/N3C)N3C4=C(/C=C\C=C/4)N4C5=C6/C(=C\43)[Cu]21[Si](C1=CC=CC=C1)(C1=CC=CC=C1)N6C1=C5C=CC=C1 HEFFZFSZEWLJNG-UHFFFAOYSA-N 0.000 description 1
- QUBBAXISAHIDNM-UHFFFAOYSA-N CCc1cccc(C)c1C Chemical compound CCc1cccc(C)c1C QUBBAXISAHIDNM-UHFFFAOYSA-N 0.000 description 1
- HWBQGPXRXROSQJ-UHFFFAOYSA-N CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]45C4=CN(C)C1=C24)O3 Chemical compound CN1C=C2C3=C4C5=C(C=C3)N(C)C3=C(C=CC=C3)N5C3=N5C6=C(C=CC7=C6N(C6=C(C=CC=C6)N7)[Si](C6=CC=CC=C6)(C6=CC=CC=C6)[Cu]45C4=CN(C)C1=C24)O3 HWBQGPXRXROSQJ-UHFFFAOYSA-N 0.000 description 1
- WDSAZCKADXJGSU-UHFFFAOYSA-N Cc1cc(-c2ccccc2)cc(C)c1-c1cc(-c2cccc(Oc(cc3)cc4c3c(cccc3)c3[n]4-c3ncccc3)c2)ncc1 Chemical compound Cc1cc(-c2ccccc2)cc(C)c1-c1cc(-c2cccc(Oc(cc3)cc4c3c(cccc3)c3[n]4-c3ncccc3)c2)ncc1 WDSAZCKADXJGSU-UHFFFAOYSA-N 0.000 description 1
- GDEQPEBFOWYWSA-UHFFFAOYSA-N Cc1cccc(C(C)C)c1C Chemical compound Cc1cccc(C(C)C)c1C GDEQPEBFOWYWSA-UHFFFAOYSA-N 0.000 description 1
- XWRYGGPOGSWLTI-KCQAQPDRSA-N Cc1cccc2c1[C@@H](C)[C@H]1CCCC[C@H]1C2 Chemical compound Cc1cccc2c1[C@@H](C)[C@H]1CCCC[C@H]1C2 XWRYGGPOGSWLTI-KCQAQPDRSA-N 0.000 description 1
- SVAHHCNTAZYUAT-UHFFFAOYSA-N O=[N+]([O-])C1=C(C2=CC=C(Br)C=C2)C=CC=C1 Chemical compound O=[N+]([O-])C1=C(C2=CC=C(Br)C=C2)C=CC=C1 SVAHHCNTAZYUAT-UHFFFAOYSA-N 0.000 description 1
- ZTAJYPQFNIZUES-UHFFFAOYSA-N O=[N+]([O-])C1=C(C2=CC=C(C3=CC=CC=N3)C=C2)C=CC=C1 Chemical compound O=[N+]([O-])C1=C(C2=CC=C(C3=CC=CC=N3)C=C2)C=CC=C1 ZTAJYPQFNIZUES-UHFFFAOYSA-N 0.000 description 1
- JOHXPNXWZBTYBQ-UHFFFAOYSA-N [H]N1C2=C(C=CC=C2)C2=C1C=C(C1=CC=CC=N1)C=C2 Chemical compound [H]N1C2=C(C=CC=C2)C2=C1C=C(C1=CC=CC=N1)C=C2 JOHXPNXWZBTYBQ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/006—Palladium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
- C07F1/08—Copper compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
- C07F1/10—Silver compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
- C07F1/12—Gold compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0033—Iridium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0073—Rhodium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0086—Platinum compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/04—Nickel compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/06—Cobalt compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic System
- C07F3/06—Zinc compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H01L51/0083—
-
- H01L51/0084—
-
- H01L51/0085—
-
- H01L51/0087—
-
- H01L51/0091—
-
- H01L51/0092—
-
- H01L51/0094—
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
- H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
- H10K50/121—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants for assisting energy transfer, e.g. sensitization
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
- H10K50/125—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/331—Metal complexes comprising an iron-series metal, e.g. Fe, Co, Ni
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/346—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising platinum
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/371—Metal complexes comprising a group IB metal element, e.g. comprising copper, gold or silver
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/381—Metal complexes comprising a group IIB metal element, e.g. comprising cadmium, mercury or zinc
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/40—Organosilicon compounds, e.g. TIPS pentacene
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
- C09K2211/1033—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with oxygen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1092—Heterocyclic compounds characterised by ligands containing sulfur as the only heteroatom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/185—Metal complexes of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/187—Metal complexes of the iron group metals, i.e. Fe, Co or Ni
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/188—Metal complexes of other metals not provided for in one of the previous groups
-
- H01L51/5012—
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/10—Triplet emission
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/20—Delayed fluorescence emission
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/27—Combination of fluorescent and phosphorescent emission
Definitions
- the present disclosure relates to metal complexes or compounds having multiple radiative decay mechanisms, together with methods for the preparation and use thereof.
- Compounds capable of absorbing and/or emitting light can be ideally suited for use in a wide variety of optical and electro-optical devices, including, for example, photo-absorbing devices such as solar- and photo-sensitive devices, photo-emitting devices, organic light emitting diodes (OLEDs), or devices capable of both photo-absorption and emission.
- photo-absorbing devices such as solar- and photo-sensitive devices
- photo-emitting devices such as organic light emitting diodes (OLEDs)
- OLEDs organic light emitting diodes
- the present invention relates to metal complexes having multiple radiative decay mechanisms, together with methods for the preparation and use thereof.
- a metal-assisted delayed fluorescent emitter represented by one or more of the formulas
- A is an accepting group comprising one or more of the following structures, which can optionally be substituted
- D is a donor group comprising of one or more of the following structures, which can optionally be substituted,
- C in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- N in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- each of a 0 , a 1 , and a 2 in dependently is present or absent, and if present, comprises a direct bond and/or linking group comprising one or more of the following
- b 1 and b 2 independently is present or absent, and if present, comprises a linking group comprising one or more of the following
- X is B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te
- Y is O, S, S ⁇ O, SO 2 , Se, N, NR 3 , PR 3 , RP ⁇ O, CR 1 R 2 , C ⁇ O, SiR 1 R 2 , GeR 1 R 2 , BH, P(O)H, PH, NH, CR 1 H, CH 2 , SiH 2 , SiHR 1 , BH, or BR 3
- each of R, R 1 , R 2 , and R 3 independently is hydrogen, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, ary
- Also disclosed are devices comprising one or more of the disclosed complexes or compounds.
- FIG. 1 is a drawing of a cross-section of an exemplary organic light-emitting diode (OLED).
- OLED organic light-emitting diode
- FIG. 2 is a schematic illustration of dual emission pathways in metal complexes, where the lowest triplet excited state (T 1 ) has a lower but similar energy level to the lowest singlet excited state (S 1 ), in accordance with various aspects of the present disclosure.
- FIG. 3 ( a ) illustrates an exemplary PdN3N complex, in accordance with various aspects of the present disclosure, wherein the UN component and D ⁇ A components are illustrated by solid and dashed lines, respectively; and (b) a UV-Vis absorption spectra of the complex illustrated in the inset, together with 77K and room temperature photoluminescence spectra of compound PdN3N.
- FIG. 4 illustrates emission spectra of a PdN3N complex at various temperatures ranging from 77 K to 340 K, in accordance with various aspects of the present disclosure.
- FIG. 5 illustrates emission spectra of a PdN1N complex in solution at 77 K and room temperature.
- FIG. 6 illustrates emission spectra of a PdN6N complex in solution at 77 K and room temperature.
- FIG. 7 illustrates emission spectra of a PdON3 — 1 complex in solution at 77 K and room temperature.
- FIG. 8 illustrates emission spectra of a PdON3 — 2 complex in solution at 77 K and room temperature.
- FIG. 9 illustrates emission spectra of a PdON3 — 3 complex in solution at 77 K and room temperature.
- FIG. 10 illustrates plots of external quantum efficiency vs. current density and the electroluminescent spectrum (inset) for the device of ITO/HATCN (10 nm)/NPD (40 nm)/TAPC (10 nm)/6% PdN3N:26mCPy (25 nm)/DPPS (10 nm)/BmPyPB (40 nm)/LiF/Al.
- FIG. 11 illustrates plots of external quantum efficiency vs. current density and the electroluminescent spectrum (inset) for the device of ITO/HATCN (10 nm)/NPD (40 nm)/6% PdN3N:CBP (25 nm)/BAlQ (10 nm)/AlQ 3 (30 nm)/LiF/Al.
- FIG. 12 illustrates plot of relative luminance at the constant current of 20 mA/cm 2 vs. operational time for the device of ITO/HATCN (10 nm)/NPD (40 nm)/6% PdN3N:CBP (25 nm)/BAlQ (10 nm)/AlQ 3 (30 nm)/LiF/Al.
- FIG. 13 illustrates plots of external quantum efficiency vs. current density and the electroluminescent spectrum (inset) for the device of ITO/HATCN (10 nm)/NPD (40 nm)/TAPC (10 nm)/6% PdN1N:26mCPy (25 nm)/DPPS (10 nm)/BmPyPB (40 nm)/LiF/Al. Additional aspects of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or can be learned by practice of the invention. The advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims. It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.
- Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another aspect includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another aspect. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint. It is also understood that there are a number of values disclosed herein, and that each value is also herein disclosed as “about” that particular value in addition to the value itself. For example, if the value “10” is disclosed, then “about 10” is also disclosed. It is also understood that each unit between two particular units are also disclosed. For example, if 10 and 15 are disclosed, then 11, 12, 13, and 14 are also disclosed.
- the terms “optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where said event or circumstance occurs and instances where it does not.
- compositions of the invention Disclosed are the components to be used to prepare the compositions of the invention as well as the compositions themselves to be used within the methods disclosed herein.
- these and other materials are disclosed herein, and it is understood that when combinations, subsets, interactions, groups, etc. of these materials are disclosed that while specific reference of each various individual and collective combinations and permutation of these compounds cannot be explicitly disclosed, each is specifically contemplated and described herein. For example, if a particular compound is disclosed and discussed and a number of modifications that can be made to a number of molecules including the compounds are discussed, specifically contemplated is each and every combination and permutation of the compound and the modifications that are possible unless specifically indicated to the contrary.
- alkyl as used herein is a branched or unbranched saturated hydrocarbon group of 1 to 24 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, n-pentyl, isopentyl, s-pentyl, neopentyl, hexyl, heptyl, octyl, nonyl, decyl, dodecyl, tetradecyl, hexadecyl, eicosyl, tetracosyl, and the like.
- the alkyl group can be cyclic or acyclic.
- the alkyl group can be branched or unbranched.
- the alkyl group can also be substituted or unsubstituted.
- the alkyl group can be substituted with one or more groups including, but not limited to, optionally substituted alkyl, cycloalkyl, alkoxy, amino, ether, halide, hydroxy, nitro, silyl, sulfo-oxo, or thiol, as described herein.
- a “lower alkyl” group is an alkyl group containing from one to six (e.g., from one to four) carbon atoms.
- amine or “amino” as used herein are represented by the formula NA 1 A 2 A 3 , where A 1 , A 2 , and A 3 can be, independently, hydrogen or optionally substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, or heteroaryl group as described herein.
- halide refers to the halogens fluorine, chlorine, bromine, and iodine.
- hydroxyl as used herein is represented by the formula —OH.
- nitro as used herein is represented by the formula —NO 2 .
- nitrile as used herein is represented by the formula —CN.
- thiol as used herein is represented by the formula —SH.
- heterocyclyl refers to cyclic structures including a heteroatom.
- heterocyclyl includes both aromatic and non-aromatic ring structures with one or more heteroatoms.
- Non-limiting examples of heterocyclic includes, pyridine, isoquinoline, methylpyrrole and thiophene etc.
- Heteroaryl specifically denotes an aromatic cyclic structure including a heteroatom.
- a dashed line outlining ring structures as used herein refers to anoptional ring structure.
- the ring structure can be aromatic or non-aromatic.
- the ring structure can comprise double bonds or can contain only single bonds within the ring structure.
- each of a 0 , a 1 , a 2 , b, b 1 , or b 2 can independently be replaced with anyone of a 0 , a 1 , a 2 , b, b 1 , and b 2 .
- b 1 in one structure can be replaced with a 1 in the same structure.
- a complex that includes more than one of the same of X, Y, a 0 , a 1 , a 2 , b, b 1 , or b 2 , then the two recited X, Y, a 0 , a 1 , a 2 , b, b 1 , or b 2 can have different structures.
- a complex recites two b 1 moieties, then the structure of one of the b 1 's can be different or the same of the other b 1 .
- Phosphorescent metal complexes have exclusive emission from the lowest triplet state. When the energy of the singlet excited state/states of metal complexes is/are closer to the energy of the lowest triplet state, metal complexes will emit simultaneously from the lowest triplet state and the singlet excited state/states at the room temperature or elevated temperature.
- metal complexes can be defined as metal-assisted delayed fluorescent emitters, and such dual emission process are defined as phosphorescence and thermal activated delayed fluorescence.
- the present invention is directed a metal complex having multiple radiative decay mechanisms.
- Metal complexes can be used for many applications including, for example, as emitters for OLEDs.
- the inventive complex can have a dual emission pathway.
- the dual emission characteristics of the inventive complex can be an enhancement of conventional phosphorescence typically found in organometallic emitters.
- the inventive complex can exhibit both a delayed fluorescence and a phosphorescence emission.
- the inventive complex can simultaneously and/or substantially simultaneously exhibit both singlet and triplet excitons.
- such an inventive complex can emit directly from a singlet excited state, so as to provide a blue-shifted emission spectrum.
- the inventive complex can be designed such that the lowest singlet excited state is thermally accessible from the lowest triplet excited state.
- emission from a complex when emission from a complex is generated primarily from the fluorescent decay of thermally populated singlets, light, for example, red, blue, and/or green light, can be produced with improved efficiency and good color purity.
- emission from a complex when emission from a complex is generated from a combination of fluorescent emission from a higher energy singlet state and phosphorescent emission from a lower energy triplet state, the overall emission of the complex can be useful to provide white light.
- the inventive complex exhibits a singlet excited state (S1) that is thermally accessible from the lowest triplet excited state (T1).
- S1 singlet excited state
- T1 triplet excited state
- this can be accomplished by tailoring the chemical structure, for example, the linkages between ligands N and C (“N ⁇ C”) and between ligands D and A (“D ⁇ A”), as illustrated in the formulas herein.
- ⁇ N can illustrate an emitting component which determines the triplet emission energy of the resulting metal complex.
- D ⁇ A can illustrate a donor-acceptor group containing the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO).
- the ⁇ N ligand and D ⁇ A ligand can optionally share or not share any structural components.
- FIG. 2 illustrates an exemplary schematic of a dual emission pathway, wherein the lowest triplet excited state (T1) has a lower, but similar energy level to the lowest singlet excited state (S1).
- the inventive complex can exhibit both a phosphorescence pathway (T1 to S0) and a delayed fluorescence pathway (S1 to S0).
- the two radiative decay processes illustrated in FIG. 2 can occur simultaneously, enabling the inventive complex to have dual emission pathways.
- the T1 state can comprise a triplet ligand-centered state (3 ⁇ N) combined with at least some charge-transfer characteristics (1D-A).
- the S1 state of the inventive complexes described herein can comprise singlet charge-transfer characteristics (1D-A).
- FIG. 2 illustrates an exemplary PdN3N complex, wherein the ⁇ N component is represented by a solid line and the D ⁇ A component is represented by a dashed line.
- a portion of the ligand structure may be shared between the ⁇ N and D ⁇ A components.
- the inventive complex can comprise a palladium based complex, referenced by PdN3N, which exhibits a blue-shifted emission spectrum at room temperature as compared to the emission spectrum at 77 K, as illustrated in FIG. 3 .
- Such an emission profile represents an emission process from an excited state with a higher energy than the T1 state.
- the intensity of at least a portion of the emission spectra can increase as the temperature increases.
- the temperature dependence indicates a thermally activated, E-type delayed fluorescence process.
- the inventive complex can comprise four coordinating ligands with a metal center.
- the inventive complex can be a tetradentate complex that can provide dual emission pathways through an emitting component and a donor-acceptor component, wherein in various aspects the emitting component and the donor-acceptor component can optionally share structural components.
- a least a portion of the structural components between the emitting component and the donor-acceptor component are shared.
- the inventive complex can be useful as, for example, a luminescent label, an emitter for an OLED, and/or in other lighting applications.
- the inventive dual emission complexes described herein can be useful as emitters in a variety of color displays and lighting applications.
- the inventive complex can provide a broad emission spectrum that can be useful, for example, in white OLEDs.
- the inventive complex can provide a deep blue emission have a narrow emission for use in, for example, a display device.
- the emission of such inventive complexes can be tuned, for example, by modifying the structure of one or more ligands.
- the compounds of the present disclosure can be prepared so as to have a desirable emission spectrum for an intended application.
- the inventive complexes can provide a broad emission spectrum, such that the complex can be useful in generating white light having a high color rendering index (CRI).
- bonds represented by an arrow indicate coordination to a metal
- bonds represented by dashed lines indicate intra-ligand bonds.
- carbon atoms in any aryl rings can optionally be substituted in any position so as to form a heterocyclic aryl ring, and can optionally have atoms, functional groups, and/or fused ring systems substituted for hydrogen at any one or more available positions on the aryl ring.
- a metal-assisted delayed fluorescent emitter wherein the energy of the singlet excited state/states is/are slightly higher (0.2 eV or less) than the energy of the lowest triplet state, and metal-assisted delayed fluorescent emitter will emit simultaneously from the lowest triplet state and the singlet excited state/states at the room temperature or elevated temperature and the metal-assisted delayed fluorescent emitter can harvest both electrogenerated singlet and triplet excitons.
- the metal-assisted delayed fluorescent emitter has 100% internal quantum efficiency in a device setting.
- a metal-assisted delayed fluorescent emitter represented by one or more of the formulas
- A is an accepting group comprising one or more of the following structures, which can optionally be substituted
- D is a donor group comprising of one or more of the following structures, which can optionally be substituted,
- C in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- N in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- each of a 0 , a 1 , and a 2 in dependently is present or absent, and if present, comprises a direct bond and/or linking group comprising one or more of the following
- b 1 and b 2 independently is present or absent, and if present, comprises a linking group comprising one or more of the following
- X is B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te
- Y is O, S, S ⁇ O, SO 2 , Se, N, NR 3 , PR 3 , RP ⁇ O, CR 1 R 2 , C ⁇ O, SiR 1 R 2 , GeR 1 R 2 , BH, P(O)H, PH, NH, CR 1 H, CH 2 , SiH 2 , SiHR 1 , BH, or BR 3
- each of R, R 1 , R 2 , and R 3 independently is hydrogen, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, ary
- M comprises a metal, wherein X, if present, comprises C, N, P, and/or Si, wherein Y, if present, comprises B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te, and wherein R, if present, can optionally represent any substituent group.
- carbon may be optionally substituted in any position(s) to form a heterocyclic aryl ring, and may have atoms, functional groups, and/or fused rings systems substituted for hydrogen along the aryl ring in any available position(s).
- the complex has the structure (a). In another aspect, the complex has the structure (b).
- M is platinum (II), palladium (II), nickel (II), manganese (II), zinc (II), gold (III), silver (III), copper (III), iridium (I), rhodium (I), or cobalt (I).
- M can be platinum (II).
- M can be palladium (II).
- M can be manganese (II).
- M can be zinc (II).
- M can be gold (III).
- M can be silver (III).
- M can be copper (III).
- M can be iridium (I).
- M can be rhodium (I).
- M can be cobalt (I).
- A is an aryl. In another aspect, A is a heteroaryl.
- a 2 is absent in structure A. In another aspect, a 2 is present in structure A. In yet another aspect, a 2 and b 2 are absent. In yet another aspect, a 2 , b 1 , and b 2 are absent. In one aspect, at least one of a 2 , b 1 , and b 2 are present.
- Y if present, can comprise a carbon, nitrogen, oxygen, silicon, phophorous, and/or sulfur, and/or a compound comprising a carbon, nitrogen, oxygen, silicon, phophorous, and/or sulfuratom.
- Y if present, comprises carbon, nitrogen, oxygen, silicon, phophorous, and/or sulfur.
- Y is N.
- Y is C.
- X is B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te.
- X can be B, C, or N.
- Y if present, can comprise boron, carbon, nitrogen, oxygen, silicon, phophorous, silicon, germanium, arsenic, selenium, tin, antimony, and/or telenium, and/or a compound comprising a boron, carbon, nitrogen, oxygen, silicon, phophorous, silicon, germanium, arsenic, selenium, tin, antimony, and/or telenium.
- X if present, comprises boron, carbon, nitrogen, oxygen, silicon, phophorous, silicon, germanium, arsenic, selenium, tin, antimony, and/or telenium
- R if present, can comprise any substituent group suitable for use in the complex and intended application. In another aspect, R, if present, comprises a group that does not adversely affect the desirable emission properties of the complex.
- A, D, C, and/or N in structures (a) or (b) can be substituted with R as described herein.
- N in structures (a) or (b) can be substituted with R, wherein R is aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl,
- C in structures (a) or (b) can be substituted with R, wherein R is aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureido, phosphoramide, amercapto, sulfo, carboxyl, hydrzino, substituted
- the dashed line outlining ring structures in A, D, C, and/or N in structures (a) or (b) represents present bonds which form a ring structure. In one aspect, the dashed line outlining ring structures in A, D, C, and/or N in structures (a) or (b) are absent. For example, the dashed lines
- A is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-phenyl
- C in structure (a) or (b) is
- N in structure (a) or (b) is
- the emitter is represented by any one of
- delayed fluorescent emitters with the structure
- M comprises Ir, Rh, Mn, Ni, Ag, Cu, or Ag;
- each of R 1 and R 2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- each of Y 1a and Y 1b independently is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- each of Y 2a , Y 2b , Y 2c , and Y 2d independently is N, NR 6a , or CR 6b , wherein each of R 6a and R 6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; each of Y 3a , Y 3b , Y 3c , Y 3d , Y 4a , Y 4b , Y 4c , and Y 4d independently is N, O, S, NR 6a , CR 6b , wherein each of R 6a and R 6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl
- n independently are an integer 1 or 2;
- each of independently is partial or full unsaturation of the ring with which it is associated.
- each of Y 1a and Y 1b independently is O, NR 2 , CR 2 R 3 or S.
- each of Y 1a and Y 1b independently is O or NR 2 .
- Y 2b is CH, wherein Y 2c , Y 3b and Y 4b is N, wherein M is Ir or Rh.
- each of Y 2 a and Y 2d is CH and each of Y 2b and Y 2c is N, then at least one of Y 4a , Y 4b , Y 3a , or Y 3d is not N.
- each of Y 2 a and Y 2d is CH and each of Y 2b and Y 2c is N, then at least one of Y 4a , Y 4b , Y 3a , or Y 3d is not N
- M comprises Pt, Pd and Au
- each of R 1 and R 2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- each of Y 1a and Y 1b independently is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- each of Y 2a , Y 2b , Y 2c , and Y 2d independently is N, NR 6a , or CR 6b , wherein each of R 6a and R 6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; each of Y 3a , Y 3b , Y 3c , Y 3d , Y 3e , Y 3f , Y 4a , Y 4b , Y 4c , and Y 4d independently is N, O, S, NR 6a , CR 6b , wherein each of R 6a and R 6b independently hydrogen, substituted or unsubstituted al
- m is an integer 1 or 2;
- each of independently is partial or full unsaturation of the ring with which it is associated.
- Y 2b and Y 2c is CH, wherein Y 3b and Y 4b is N, and wherein M is Pt or Pd.
- Y 2b and Y 2c is CH, wherein Y 3b and Y 4b is N, wherein each of Y 1a and Y 1b independently is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure; herein M is Pt or Pd.
- Y 2b , Y 2c and Y 4b is CH, wherein Y 3b , is N, wherein each of Y 1a and Y 1b independently is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure; wherein M is Au.
- Y 2b and Y 2c is CH, wherein Y 3b and Y 4b is N, wherein one of Y 1a and Y 1b is B(R 2 ) 2 and the other of Y 1a and Y 1b is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby
- m is 1, each of Y 2 a and Y 2d is CH and each of Y 2b and Y 2c is N, then at least one of Y 4a , Y 4b , Y 3a , Y 3d is not N.
- a metal-assisted delayed fluorescent emitters having the structure:
- M comprises Ir, Rh, Pt, Os, Zr, Co, or Ru;
- each of R 1 and R 2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- each of Y 1a , Y 1b , Y 1c and Y 1d independently is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- Y 1e is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, or nothing, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- each of Y 2a , Y 2b , Y 2c , and Y 2d independently is N, NR 6a , or CR 6b , wherein each of R 6a and R 6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- each of Y 3a , Y 3b , Y 3c , Y 3d , Y 3e , Y 4a , Y 4b , Y 4c , and Y 4d independently is N, O, S, NR 6a , CR 6b , wherein each of R 6a and R 6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R 6c ) 2 , wherein Z is C or Si, and wherein each R 6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloal
- each of Y 5a , Y 5b , Y 5c , Y 5d , Y 6a , Y 6b , Y 6c , and Y 6d independently is N, O, S, NR 6a , or CR 6b ;
- each of m, n, l and p independently are an integer 1 or 2; wherein each of independently is partial or full unsaturation of the ring with which it is associated.
- a metal-assisted delayed fluorescent emitters having the structure
- M comprises Pd, Ir, Rh, Au, Co, Mn, Ni, Ag, or Cu;
- each of Y 1a and Y 1b independently is O, NR 2 , CR 2 R 3 , S, AsR 2 , BR 2 , B(R 2 ) 2 ,PR 2 , P(O)R 2 , or SiR 2 R 3 , or a combination thereof, wherein each of R 2 and R 3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R 2 and R 3 together form C ⁇ O, wherein each of R 2 and R 3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- each of Y 2a , Y 2b , Y 2c , Y 2d , Y 2e , Y 2f , Y 2g , and Y 2h independently is N, NR 6a , or CR 6b , wherein each of R 6a and R 6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- each of Y 3a , Y 3b , Y 3c , Y 3d , Y 3e , Y 4a , Y 4b , Y 4c , Y 4d , and Y 4e independently is N, O, S, NR 6a , CR 6b , wherein each of R 6a and R 6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R 6c ) 2 , wherein Z is C or Si, and wherein each R 6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane
- m is an integer 1 or 2;
- n is an integer 1 or 2;
- each of independently is partial or full unsaturation of the ring with which it is associated.
- each of Fl 1 , Fl 2 , Fl 3 and Fl 4 independently are fluorescent emitters with tunable singlet excited state energies which are covenantly bonded to selected atoms among Y 2a , Y 2d , Y 2e , Y 2f , Y 2g , Y 2h , Y 3c , Y 3d , Y 3e , Y 4c , Y 4d , and Y 4e .
- the inventive complex can exhibit an overall neutral charge. In another aspect, the inventive complex can exhibit a non-neutral overall charge. In other aspects, the metal center of the inventive complex can comprise a metal having a +1, a +2, and/or a +3 oxidation state.
- the inventive complex can comprise a neutral complex having the structure
- M represents a metal having a +1 oxidation state.
- the inventive complex can comprise a neutral complex having the structure
- M represents a metal having a +1 oxidation state.
- the inventive complex can comprise a neutral complex having the structure
- M represents a metal having a +2 oxidation state.
- the inventive complex can comprise a neutral complex having the structure
- the inventive complex can comprise a neutral complex having the structure
- M represents a metal having a +3 oxidation state.
- such an inventive complex can comprise any one or more of the following:
- such an inventive complex can comprise any one or more of the following:
- such an inventive complex can comprise any one or more of the following:
- the inventive complex can comprise a neutral complex having the structure
- M represents a metal having a +2 oxidation state.
- such an inventive complex can comprise any one or more of the following:
- such an inventive complex can comprise any one or more of the following:
- such an inventive complex can comprise any one or more of the following:
- each A independently is O, S, NR, PR, AsR, CR 2 , SiR 2 , or BR, wherein each U independently is O S, NR, PR, AsR, CR 2 , SiR 2 , or BR, wherein M is Pt or Pd, and
- a disclosed complex can have the structure:
- each U independently is O S, NR, PR, AsR, CR 2 , SiR 2 , or BR, wherein M is Mn or Ni, and wherein
- a disclosed complex can have the structure:
- each A independently is O, S, NR, PR, AsR, CR 2 , SiR 2 , or BR, wherein each U independently is O S, NR, PR, AsR, CR 2 , SiR 2 , or BR, wherein M is Ir, Rh, or Cu, and wherein
- a disclosed compound can have the structure:
- each A independently is O, S, NR, PR, AsR, CR 2 , SiR 2 , or BR,
- each U independently is O S, NR, PR, AsR, CR 2 , SiR 2 , or BR,
- M is Au or Ag
- a disclosed complex can have the structure:
- FL groups are covalently bonded to any component of metal complexes including the Ar 1 group.
- each A independently is O, S, NR, PR, AsR, CR 2 , SiR 2 , BR, or BR 2 ,
- each U independently is O S, NR, PR, AsR, CR 2 , SiR 2 , or BR,
- M is Pd, Mn, Ni, Ir, Rh, Cu, Au, or Ag,
- FL is covalently bonded to any component of the complex, for example, the Ar 1 group;
- the FL group is covalently bonded to the Ar 1 group.
- any one or more of the compounds disclosed herein can be excluded from the present invention.
- inventive complexes described herein can be prepared according to methods such as those provide in the Examples or that one of skill in the art, in possession of this disclosure, could readily discern from this disclosure and from methods known in the art.
- compositions disclosed here can be used as host materials for OLED applications, such as full color displays.
- the organic light emitting diodes with metal-assisted delayed fluorescent emitters can have the potential of harvesting both electrogenerated singlet and triplet excitons and achieving 100% internal quantum efficiency in the device settings.
- the component of delayed fluorescence process will occurred at a higher energy than that of phosphorescence process, which can provide a blue-shifted emission spectrum than those originated exclusively from the lowest triplet excited state of metal complexes.
- the existence of metal ions (especially the heavy metal ions) will facilitate the phosphorescent emission inside of the emitters, ensuring a high emission quantum efficiency.
- the energy of the singlet excited states of metal-assisted delayed fluorescent emitters can be adjusted separately from the lowest triplet excited by ether modifying the energy of donor-accepter ligands or attaching fluorescent emitters which are covalently bonded to metal complexes without having effective conjugation between fluorescent emitters and metal complexes.
- compositions of the present disclosure can be useful in a wide variety of applications, such as, for example, lighting devices.
- one or more of the complexes can be useful as host materials for an organic light emitting display device.
- the compounds of the invention are useful in a variety of applications.
- the compounds can be useful in organic light emitting diodes (OLED)s, luminescent devices and displays, and other light emitting devices.
- OLED organic light emitting diodes
- the energy profile of the compounds can be tuned by varying the structure of the ligand surrounding the metal center. For example, compounds having a ligand with electron withdrawing substituents will generally exhibit different properties, than compounds having a ligand with electron donating substituents. Generally, a chemical structural change affects the electronic structure of the compound, which thereby affects the electrical transport and transfer functions of the material. Thus, the compounds of the present invention can be tailored or tuned to a specific application that desires an energy or transport characteristic.
- inventive compositions can provide improved efficiency and/or operational lifetimes in lighting devices, such as, for example, organic light emitting devices, as compared to conventional materials.
- inventive compositions can be useful as, for example, host materials for organic light emitting diodes, lighting applications, and combinations thereof.
- the compound in the device is selected to have 100% internal quantum efficiency in the device settings.
- the device is an organic light emitting diode. In another aspect, the device is a full color display. In yet another aspect, the device is an organic solid state lighting
- FIG. 1 shows a cross-sectional view of an OLED 100 , which includes substrate 102 with an anode 104 , which is typically a transparent material, such as indium tin oxide, a layer of hole-transporting material(s) (HTL) 106 , a layer of light processing material 108 , such as an emissive material (EML) including an emitter and a host, a layer of electron-transporting material(s) (ETL) 110 , and a metal cathode layer 112 .
- an OLED 100 which includes substrate 102 with an anode 104 , which is typically a transparent material, such as indium tin oxide, a layer of hole-transporting material(s) (HTL) 106 , a layer of light processing material 108 , such as an emissive material (EML) including an emitter and a host, a layer of electron-transporting material(s) (ETL) 110 , and a metal cathode layer 112 .
- a light emitting device such as, for example, an OLED
- any of the one or more layers can comprise indium tin oxide (ITO), poly(3,4-ethylenedioxythiophene) (PEDOT), polystyrene sulfonate (PSS), N,N′-di-1-naphthyl-N,N′-diphenyl-1,1′-biphenyl-4,4′diamine (NPD), 1,1-bis((di-4-tolylamino)phenyl) cyclohexane (TAPC), 2,6-Bis(N-carbazolyl)pyridine (mCpy), 2,8-bis(diphenylphosphoryl)dibenzothiophene (PO15), LiF, Al, or a combination thereof.
- any of the one or more layers can comprise a material not specifically recited herein.
- the layer of light processing material 108 can comprise one or more compounds of the present invention optionally together with a host material.
- the host material can be any suitable host material known in the art.
- the emission color of an OLED is determined by the emission energy (optical energy gap) of the light processing material 108 , which as discussed above can be tuned by tuning the electronic structure of the emitting compounds and/or the host material.
- Both the hole-transporting material in the HTL layer 106 and the electron-transporting material(s) in the ETL layer 110 can comprise any suitable hole-transporter known in the art. A selection of which is well within the purview of those skilled in the art.
- Phosphorescent OLEDs i.e., OLEDs with phosphorescent emitters
- OLEDs with phosphorescent emitters typically have higher device efficiencies than other OLEDs, such as fluorescent OLEDs.
- Light emitting devices based on electrophosphorescent emitters are described in more detail in WO2000/070655 to Baldo et al., which is incorporated herein by this reference for its teaching of OLEDs, and in particular phosphorescent OLEDs.
- the compounds of the invention can be made using a variety of methods, including, but not limited to those recited in the examples provided herein. In other aspects, one of skill in the art, in possession of this disclosure, could readily determine an appropriate method for the preparation of an iridium complex as recited herein.
- a PdN3N complex can be prepared based on the following examples.
- a vessel was charged with 5 mmol 4′-bromo-2-nitrobiphenyl, 12.5 mmol 2-(tributylstannyl)pyridine, 0.25 mmol tetrakistriphenylphosphine palladium(0), 20 mmol potassium fluoride, and 75 mL anhydrous, degassed toluene.
- the vessel was set to reflux under a nitrogen atmosphere for 3 days.
- the resulting solution was cooled, the solids filtered off, and poured into a stirring aqueous solution of potassium fluoride.
- the organic phase was collected, washed once more with aqueous potassium fluoride, and dried of magnesium sulfate.
- the solvent was removed under reduced pressure and the crude product was chromatographed over silica initially with hexane followed by dichloromethane to yield a viscous, colorless oil in 60% yield.
Abstract
Metal complexes that exhibit multiple radiative decay mechanisms, together with methods for the preparation and use thereof.
Description
- This invention was made with government support under grant number 0748867, awarded by the National Science Foundation. The government has certain rights in the invention.
- 1. Technical Field
- The present disclosure relates to metal complexes or compounds having multiple radiative decay mechanisms, together with methods for the preparation and use thereof.
- 2. Technical Background
- Compounds capable of absorbing and/or emitting light can be ideally suited for use in a wide variety of optical and electro-optical devices, including, for example, photo-absorbing devices such as solar- and photo-sensitive devices, photo-emitting devices, organic light emitting diodes (OLEDs), or devices capable of both photo-absorption and emission. Much research has been devoted to the discovery and optimization of organic and organometallic materials for using in optical and electro-optical devices. Metal complexes can be used for many applications, including as emitters use in for OLEDs.
- Despite advances in research devoted to optical and electro-optical materials, many currently available materials exhibit a number of disadvantages, including poor processing ability, inefficient mission or absorption, and less than ideal stability, among others. Thus, a need exists for new materials which exhibit improved performance in optical and electro-optical devices. This need and other needs are satisfied by the present invention.
- The present invention relates to metal complexes having multiple radiative decay mechanisms, together with methods for the preparation and use thereof.
- In one aspect, Disclosed herein is a metal-assisted delayed fluorescent emitter represented by one or more of the formulas
- wherein A is an accepting group comprising one or more of the following structures, which can optionally be substituted
- wherein D is a donor group comprising of one or more of the following structures, which can optionally be substituted,
- wherein C in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- wherein N in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- wherein each of a0, a1, and a2 in dependently is present or absent, and if present, comprises a direct bond and/or linking group comprising one or more of the following
- wherein b1 and b2 independently is present or absent, and if present, comprises a linking group comprising one or more of the following
- wherein X is B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te, wherein Y is O, S, S═O, SO2, Se, N, NR3, PR3, RP═O, CR1R2, C═O, SiR1R2, GeR1R2, BH, P(O)H, PH, NH, CR1H, CH2, SiH2, SiHR1, BH, or BR3,
wherein each of R, R1, R2, and R3 independently is hydrogen, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureido, phosphoramide, amercapto, sulfo, carboxyl, hydrzino, substituted silyl, or polymerizable, or any conjugate or combination thereof,
wherein n is a number that satisfies the valency of Y,
wherein M is platinum (II), palladium (II), nickel (II), manganese (II), zinc (II), gold (III), silver (III), copper (III), iridium (I), rhodium (I), or cobalt (I). - Also disclosed are devices comprising one or more of the disclosed complexes or compounds.
- The accompanying figures, which are incorporated in and constitute a part of this specification, illustrate several aspects and together with the description serve to explain the principles of the invention.
-
FIG. 1 is a drawing of a cross-section of an exemplary organic light-emitting diode (OLED). -
FIG. 2 is a schematic illustration of dual emission pathways in metal complexes, where the lowest triplet excited state (T1) has a lower but similar energy level to the lowest singlet excited state (S1), in accordance with various aspects of the present disclosure. -
FIG. 3 (a) illustrates an exemplary PdN3N complex, in accordance with various aspects of the present disclosure, wherein the UN component and D̂A components are illustrated by solid and dashed lines, respectively; and (b) a UV-Vis absorption spectra of the complex illustrated in the inset, together with 77K and room temperature photoluminescence spectra of compound PdN3N. -
FIG. 4 illustrates emission spectra of a PdN3N complex at various temperatures ranging from 77 K to 340 K, in accordance with various aspects of the present disclosure. -
FIG. 5 illustrates emission spectra of a PdN1N complex in solution at 77 K and room temperature. -
FIG. 6 illustrates emission spectra of a PdN6N complex in solution at 77 K and room temperature. -
FIG. 7 illustrates emission spectra of aPdON3 —1 complex in solution at 77 K and room temperature. -
FIG. 8 illustrates emission spectra of aPdON3 —2 complex in solution at 77 K and room temperature. -
FIG. 9 illustrates emission spectra of aPdON3 —3 complex in solution at 77 K and room temperature. -
FIG. 10 illustrates plots of external quantum efficiency vs. current density and the electroluminescent spectrum (inset) for the device of ITO/HATCN (10 nm)/NPD (40 nm)/TAPC (10 nm)/6% PdN3N:26mCPy (25 nm)/DPPS (10 nm)/BmPyPB (40 nm)/LiF/Al. -
FIG. 11 illustrates plots of external quantum efficiency vs. current density and the electroluminescent spectrum (inset) for the device of ITO/HATCN (10 nm)/NPD (40 nm)/6% PdN3N:CBP (25 nm)/BAlQ (10 nm)/AlQ3 (30 nm)/LiF/Al. -
FIG. 12 illustrates plot of relative luminance at the constant current of 20 mA/cm2 vs. operational time for the device of ITO/HATCN (10 nm)/NPD (40 nm)/6% PdN3N:CBP (25 nm)/BAlQ (10 nm)/AlQ3 (30 nm)/LiF/Al. -
FIG. 13 illustrates plots of external quantum efficiency vs. current density and the electroluminescent spectrum (inset) for the device of ITO/HATCN (10 nm)/NPD (40 nm)/TAPC (10 nm)/6% PdN1N:26mCPy (25 nm)/DPPS (10 nm)/BmPyPB (40 nm)/LiF/Al. Additional aspects of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or can be learned by practice of the invention. The advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims. It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed. - The present invention can be understood more readily by reference to the following detailed description of the invention and the Examples included therein.
- Before the present compounds, devices, and/or methods are disclosed and described, it is to be understood that they are not limited to specific synthetic methods unless otherwise specified, or to particular reagents unless otherwise specified, as such can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only and is not intended to be limiting. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, example methods and materials are now described.
- As used in the specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a component” includes mixtures of two or more components.
- Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another aspect includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another aspect. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint. It is also understood that there are a number of values disclosed herein, and that each value is also herein disclosed as “about” that particular value in addition to the value itself. For example, if the value “10” is disclosed, then “about 10” is also disclosed. It is also understood that each unit between two particular units are also disclosed. For example, if 10 and 15 are disclosed, then 11, 12, 13, and 14 are also disclosed.
- As used herein, the terms “optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where said event or circumstance occurs and instances where it does not.
- Disclosed are the components to be used to prepare the compositions of the invention as well as the compositions themselves to be used within the methods disclosed herein. These and other materials are disclosed herein, and it is understood that when combinations, subsets, interactions, groups, etc. of these materials are disclosed that while specific reference of each various individual and collective combinations and permutation of these compounds cannot be explicitly disclosed, each is specifically contemplated and described herein. For example, if a particular compound is disclosed and discussed and a number of modifications that can be made to a number of molecules including the compounds are discussed, specifically contemplated is each and every combination and permutation of the compound and the modifications that are possible unless specifically indicated to the contrary. Thus, if a class of molecules A, B, and C are disclosed as well as a class of molecules D, E, and F and an example of a combination molecule, A-D is disclosed, then even if each is not individually recited each is individually and collectively contemplated meaning combinations, A-E, A-F, B-D, B-E, B-F, C-D, C-E, and C—F are considered disclosed. Likewise, any subset or combination of these is also disclosed. Thus, for example, the sub-group of A-E, B-F, and C-E would be considered disclosed. This concept applies to all aspects of this application including, but not limited to, steps in methods of making and using the compositions of the invention. Thus, if there are a variety of additional steps that can be performed it is understood that each of these additional steps can be performed with any specific embodiment or combination of embodiments of the methods of the invention.
- The term “alkyl” as used herein is a branched or unbranched saturated hydrocarbon group of 1 to 24 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, n-pentyl, isopentyl, s-pentyl, neopentyl, hexyl, heptyl, octyl, nonyl, decyl, dodecyl, tetradecyl, hexadecyl, eicosyl, tetracosyl, and the like. The alkyl group can be cyclic or acyclic. The alkyl group can be branched or unbranched. The alkyl group can also be substituted or unsubstituted. For example, the alkyl group can be substituted with one or more groups including, but not limited to, optionally substituted alkyl, cycloalkyl, alkoxy, amino, ether, halide, hydroxy, nitro, silyl, sulfo-oxo, or thiol, as described herein. A “lower alkyl” group is an alkyl group containing from one to six (e.g., from one to four) carbon atoms.
- The terms “amine” or “amino” as used herein are represented by the formula NA1A2A3, where A1, A2, and A3 can be, independently, hydrogen or optionally substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, or heteroaryl group as described herein.
- The term “halide” as used herein refers to the halogens fluorine, chlorine, bromine, and iodine.
- The term “hydroxyl” as used herein is represented by the formula —OH.
- The term “nitro” as used herein is represented by the formula —NO2.
- The term “nitrile” as used herein is represented by the formula —CN.
- The term “thiol” as used herein is represented by the formula —SH.
- The term “heterocyclyl” or the like terms refer to cyclic structures including a heteroatom. Thus, “heterocyclyl” includes both aromatic and non-aromatic ring structures with one or more heteroatoms. Non-limiting examples of heterocyclic includes, pyridine, isoquinoline, methylpyrrole and thiophene etc. “Heteroaryl” specifically denotes an aromatic cyclic structure including a heteroatom.
- A dashed line outlining ring structures as used herein refers to anoptional ring structure. The ring structure can be aromatic or non-aromatic. For example, the ring structure can comprise double bonds or can contain only single bonds within the ring structure. For example,
- can have the structure
- In one aspect, as used herein each of a0, a1, a2, b, b1, or b2 can independently be replaced with anyone of a0, a1, a2, b, b1, and b2. For example, b1 in one structure can be replaced with a1 in the same structure.
- In one aspect, a complex that includes more than one of the same of X, Y, a0, a1, a2, b, b1, or b2, then the two recited X, Y, a0, a1, a2, b, b1, or b2 can have different structures. For example, if a complex recites two b1 moieties, then the structure of one of the b1's can be different or the same of the other b1.
- Phosphorescent metal complexes have exclusive emission from the lowest triplet state. When the energy of the singlet excited state/states of metal complexes is/are closer to the energy of the lowest triplet state, metal complexes will emit simultaneously from the lowest triplet state and the singlet excited state/states at the room temperature or elevated temperature. Such metal complexes can be defined as metal-assisted delayed fluorescent emitters, and such dual emission process are defined as phosphorescence and thermal activated delayed fluorescence.
- As briefly described above, the present invention is directed a metal complex having multiple radiative decay mechanisms. Metal complexes can be used for many applications including, for example, as emitters for OLEDs. In another aspect, the inventive complex can have a dual emission pathway. In one aspect, the dual emission characteristics of the inventive complex can be an enhancement of conventional phosphorescence typically found in organometallic emitters. In another aspect, the inventive complex can exhibit both a delayed fluorescence and a phosphorescence emission. In yet another aspect, the inventive complex can simultaneously and/or substantially simultaneously exhibit both singlet and triplet excitons. In one aspect, such an inventive complex can emit directly from a singlet excited state, so as to provide a blue-shifted emission spectrum. In another aspect, the inventive complex can be designed such that the lowest singlet excited state is thermally accessible from the lowest triplet excited state.
- In one aspect, when emission from a complex is generated primarily from the fluorescent decay of thermally populated singlets, light, for example, red, blue, and/or green light, can be produced with improved efficiency and good color purity. In another aspect, when emission from a complex is generated from a combination of fluorescent emission from a higher energy singlet state and phosphorescent emission from a lower energy triplet state, the overall emission of the complex can be useful to provide white light.
- In one aspect, the inventive complex exhibits a singlet excited state (S1) that is thermally accessible from the lowest triplet excited state (T1). In another aspect, and while not wishing to be bound by theory, this can be accomplished by tailoring the chemical structure, for example, the linkages between ligands N and C (“N̂C”) and between ligands D and A (“D̂A”), as illustrated in the formulas herein. In one aspect, ĈN can illustrate an emitting component which determines the triplet emission energy of the resulting metal complex. In another aspect, D̂A can illustrate a donor-acceptor group containing the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO). In various aspects, the ĈN ligand and D̂A ligand can optionally share or not share any structural components.
- With reference to the figures,
FIG. 2 illustrates an exemplary schematic of a dual emission pathway, wherein the lowest triplet excited state (T1) has a lower, but similar energy level to the lowest singlet excited state (S1). Thus, the inventive complex can exhibit both a phosphorescence pathway (T1 to S0) and a delayed fluorescence pathway (S1 to S0). The two radiative decay processes illustrated inFIG. 2 can occur simultaneously, enabling the inventive complex to have dual emission pathways. In the inventive complexes described herein, the T1 state can comprise a triplet ligand-centered state (3ĈN) combined with at least some charge-transfer characteristics (1D-A). Similarly, the S1 state of the inventive complexes described herein can comprise singlet charge-transfer characteristics (1D-A).FIG. 2 illustrates an exemplary PdN3N complex, wherein the ĈN component is represented by a solid line and the D̂A component is represented by a dashed line. In such an inventive complex, a portion of the ligand structure may be shared between the ĈN and D̂A components. - In a specific aspect, the inventive complex can comprise a palladium based complex, referenced by PdN3N, which exhibits a blue-shifted emission spectrum at room temperature as compared to the emission spectrum at 77 K, as illustrated in
FIG. 3 . Such an emission profile represents an emission process from an excited state with a higher energy than the T1 state. - In one aspect, the intensity of at least a portion of the emission spectra, for example, from about 480 nm to about 500 nm, can increase as the temperature increases. In such an aspect, the temperature dependence indicates a thermally activated, E-type delayed fluorescence process.
- In one aspect, the inventive complex can comprise four coordinating ligands with a metal center. In another aspect, the inventive complex can be a tetradentate complex that can provide dual emission pathways through an emitting component and a donor-acceptor component, wherein in various aspects the emitting component and the donor-acceptor component can optionally share structural components. In one aspect, a least a portion of the structural components between the emitting component and the donor-acceptor component are shared. In another aspect, there are no shared structural components between the emitting and donor-acceptor components of the complex.
- In another aspect, the inventive complex can be useful as, for example, a luminescent label, an emitter for an OLED, and/or in other lighting applications. In one aspect, the inventive dual emission complexes described herein can be useful as emitters in a variety of color displays and lighting applications. In one aspect, the inventive complex can provide a broad emission spectrum that can be useful, for example, in white OLEDs. In another aspect, the inventive complex can provide a deep blue emission have a narrow emission for use in, for example, a display device.
- In another aspect, the emission of such inventive complexes can be tuned, for example, by modifying the structure of one or more ligands. In one aspect, the compounds of the present disclosure can be prepared so as to have a desirable emission spectrum for an intended application. In another aspect, the inventive complexes can provide a broad emission spectrum, such that the complex can be useful in generating white light having a high color rendering index (CRI).
- In any of the formulas and/or chemical structures recited herein, bonds represented by an arrow indicate coordination to a metal, whereas bonds represented by dashed lines indicate intra-ligand bonds. In addition, carbon atoms in any aryl rings can optionally be substituted in any position so as to form a heterocyclic aryl ring, and can optionally have atoms, functional groups, and/or fused ring systems substituted for hydrogen at any one or more available positions on the aryl ring.
- Disclosed herein is a metal-assisted delayed fluorescent emitter, wherein the energy of the singlet excited state/states is/are slightly higher (0.2 eV or less) than the energy of the lowest triplet state, and metal-assisted delayed fluorescent emitter will emit simultaneously from the lowest triplet state and the singlet excited state/states at the room temperature or elevated temperature and the metal-assisted delayed fluorescent emitter can harvest both electrogenerated singlet and triplet excitons.
- In one aspect, the metal-assisted delayed fluorescent emitter has 100% internal quantum efficiency in a device setting.
- Disclosed herein is a metal-assisted delayed fluorescent emitter represented by one or more of the formulas
- wherein A is an accepting group comprising one or more of the following structures, which can optionally be substituted
- wherein D is a donor group comprising of one or more of the following structures, which can optionally be substituted,
- wherein C in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- wherein N in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
- wherein each of a0, a1, and a2 in dependently is present or absent, and if present, comprises a direct bond and/or linking group comprising one or more of the following
- wherein b1 and b2 independently is present or absent, and if present, comprises a linking group comprising one or more of the following
- wherein X is B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te,
wherein Y is O, S, S═O, SO2, Se, N, NR3, PR3, RP═O, CR1R2, C═O, SiR1R2, GeR1R2, BH, P(O)H, PH, NH, CR1H, CH2, SiH2, SiHR1, BH, or BR3, wherein each of R, R1, R2, and R3 independently is hydrogen, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureido, phosphoramide, amercapto, sulfo, carboxyl, hydrzino, substituted silyl, or polymerizable, or any conjugate or combination thereof,
wherein n is a number that satisfies the valency of Y,
wherein M is platinum (II), palladium (II), nickel (II), manganese (II), zinc (II), gold (III), silver (III), copper (III), iridium (I), rhodium (I), or cobalt (I). - In one aspect, in:
- M comprises a metal, wherein X, if present, comprises C, N, P, and/or Si, wherein Y, if present, comprises B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te, and wherein R, if present, can optionally represent any substituent group. Furthermore, in all aryl rings depicted, carbon may be optionally substituted in any position(s) to form a heterocyclic aryl ring, and may have atoms, functional groups, and/or fused rings systems substituted for hydrogen along the aryl ring in any available position(s).
- In one aspect, the complex has the structure (a). In another aspect, the complex has the structure (b).
- In one aspect, M is platinum (II), palladium (II), nickel (II), manganese (II), zinc (II), gold (III), silver (III), copper (III), iridium (I), rhodium (I), or cobalt (I). For example, M can be platinum (II). In another example, M can be palladium (II). In yet another example, M can be manganese (II). In yet another example, M can be zinc (II). In yet another example, M can be gold (III). In yet another example, M can be silver (III). In yet another example, M can be copper (III). In yet another example, M can be iridium (I). In yet another example, M can be rhodium (I). In yet another example, M can be cobalt (I).
- In one aspect, A is an aryl. In another aspect, A is a heteroaryl.
- In one aspect, a2 is absent in structure A. In another aspect, a2 is present in structure A. In yet another aspect, a2 and b2 are absent. In yet another aspect, a2, b1, and b2 are absent. In one aspect, at least one of a2, b1, and b2 are present.
- In another aspect, Y, if present, can comprise a carbon, nitrogen, oxygen, silicon, phophorous, and/or sulfur, and/or a compound comprising a carbon, nitrogen, oxygen, silicon, phophorous, and/or sulfuratom. In a specific aspect, Y, if present, comprises carbon, nitrogen, oxygen, silicon, phophorous, and/or sulfur. In one aspect, Y is N. In another aspect, Y is C.
- In one aspect, X is B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te. For example, X can be B, C, or N. In another aspect, Y, if present, can comprise boron, carbon, nitrogen, oxygen, silicon, phophorous, silicon, germanium, arsenic, selenium, tin, antimony, and/or telenium, and/or a compound comprising a boron, carbon, nitrogen, oxygen, silicon, phophorous, silicon, germanium, arsenic, selenium, tin, antimony, and/or telenium. In a specific aspect, X, if present, comprises boron, carbon, nitrogen, oxygen, silicon, phophorous, silicon, germanium, arsenic, selenium, tin, antimony, and/or telenium
- In yet another aspect, R, if present, can comprise any substituent group suitable for use in the complex and intended application. In another aspect, R, if present, comprises a group that does not adversely affect the desirable emission properties of the complex.
- In one aspect, A, D, C, and/or N in structures (a) or (b) can be substituted with R as described herein. For example, N in structures (a) or (b) can be substituted with R, wherein R is aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureido, phosphoramide, amercapto, sulfo, carboxyl, hydrzino, substituted silyl, or polymerizable, or any conjugate or combination thereof. In another example, C in structures (a) or (b) can be substituted with R, wherein R is aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureido, phosphoramide, amercapto, sulfo, carboxyl, hydrzino, substituted silyl, or polymerizable, or any conjugate or combination thereof.
- In one aspect, the dashed line outlining ring structures in A, D, C, and/or N in structures (a) or (b) represents present bonds which form a ring structure. In one aspect, the dashed line outlining ring structures in A, D, C, and/or N in structures (a) or (b) are absent. For example, the dashed lines
- in one aspect represents present bonds and in another aspect are absent.
- In one aspect, A is
- wherein a2 is absent, wherein b2 are absent, wherein D is
- In another aspect, C in structure (a) or (b) is
- In another aspect, N in structure (a) or (b) is
- or R substituted
- In one aspect, the emitter is represented by any one of
- Also disclosed herein are delayed fluorescent emitters with the structure
- wherein M comprises Ir, Rh, Mn, Ni, Ag, Cu, or Ag;
- wherein each of R1 and R2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- wherein each of Y2a, Y2b, Y2c, and Y2d independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; each of Y3a, Y3b, Y3c, Y3d, Y4a, Y4b, Y4c, and Y4d independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein each of m and n independently are an
integer -
- In one aspect, each of Y1a and Y1b independently is O, NR2, CR2R3 or S. For example, each of Y1a and Y1b independently is O or NR2.
- In one aspect, Y2b is CH, wherein Y2c, Y3b and Y4b is N, wherein M is Ir or Rh.
- In one aspect, if m is 1, each of Y2 a and Y2d is CH and each of Y2b and Y2c is N, then at least one of Y4a, Y4b, Y3a, or Y3d is not N.
- In one aspect, if n is 1, each of Y2 a and Y2d is CH and each of Y2b and Y2c is N, then at least one of Y4a, Y4b, Y3a, or Y3d is not N
- Also disclosed herein is a metal-assisted delayed fluorescent emitters having the structure
- wherein M comprises Pt, Pd and Au;
- wherein each of R1 and R2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- wherein each of Y2a, Y2b, Y2c, and Y2d independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; each of Y3a, Y3b, Y3c, Y3d, Y3e, Y3f, Y4a, Y4b, Y4c, and Y4d independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein each of m is an
integer -
- In one aspect, Y2b and Y2c is CH, wherein Y3b and Y4b is N, and wherein M is Pt or Pd.
- In one aspect, Y2b and Y2c is CH, wherein Y3b and Y4b is N, wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure; herein M is Pt or Pd.
- In one aspect, Y2b, Y2c and Y4b is CH, wherein Y3b, is N, wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure; wherein M is Au.
- In one aspect, Y2b and Y2c is CH, wherein Y3b and Y4b is N, wherein one of Y1a and Y1b is B(R2)2 and the other of Y1a and Y1b is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure; wherein M is Au.
- In one aspect, m is 1, each of Y2 a and Y2d is CH and each of Y2b and Y2c is N, then at least one of Y4a, Y4b, Y3a, Y3d is not N.
- Also disclosed herein is a metal-assisted delayed fluorescent emitters having the structure:
- wherein M comprises Ir, Rh, Pt, Os, Zr, Co, or Ru;
- wherein each of R1 and R2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein each of Y1a, Y1b, Y1c and Y1d independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- wherein Y1e is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, or nothing, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- wherein each of Y2a, Y2b, Y2c, and Y2d independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein each of Y3a, Y3b, Y3c, Y3d, Y3e, Y4a, Y4b, Y4c, and Y4d independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein in each of each of Y5a, Y5b, Y5c, Y5d, Y6a, Y6b, Y6c, and Y6d independently is N, O, S, NR6a, or CR6b;
-
- A metal-assisted delayed fluorescent emitters having the structure
- wherein M comprises Pd, Ir, Rh, Au, Co, Mn, Ni, Ag, or Cu;
- wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, B(R2)2,PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
- wherein each of Y2a, Y2b, Y2c, Y2d, Y2e, Y2f, Y2g, and Y2h independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- each of Y3a, Y3b, Y3c, Y3d, Y3e, Y4a, Y4b, Y4c, Y4d, and Y4e independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
- wherein each of m is an
integer - wherein each of n is an
integer -
- wherein each of Fl1, Fl2, Fl3 and Fl4 independently are fluorescent emitters with tunable singlet excited state energies which are covenantly bonded to selected atoms among Y2a, Y2d, Y2e, Y2f, Y2g, Y2h, Y3c, Y3d, Y3e, Y4c, Y4d, and Y4e.
- In one aspect, the inventive complex can exhibit an overall neutral charge. In another aspect, the inventive complex can exhibit a non-neutral overall charge. In other aspects, the metal center of the inventive complex can comprise a metal having a +1, a +2, and/or a +3 oxidation state.
- In one aspect, the inventive complex can comprise a neutral complex having the structure
- wherein the M represents a metal having a +1 oxidation state.
- In another aspect, the inventive complex can comprise a neutral complex having the structure
- wherein the M represents a metal having a +1 oxidation state.
- In one aspect, the inventive complex can comprise a neutral complex having the structure
- wherein the M represents a metal having a +2 oxidation state.
- In one aspect, the inventive complex can comprise a neutral complex having the structure
- wherein the M represents a metal having a +3 oxidation state. In another aspect, the inventive complex can comprise a neutral complex having the structure
- wherein the M represents a metal having a +3 oxidation state.
- In various aspects, such an inventive complex can comprise any one or more of the following:
- In various aspects, such an inventive complex can comprise any one or more of the following:
- In various aspects, such an inventive complex can comprise any one or more of the following:
- In another aspect, the inventive complex can comprise a neutral complex having the structure
- wherein the M represents a metal having a +2 oxidation state.
- In various aspects, such an inventive complex can comprise any one or more of the following:
- In various aspects, such an inventive complex can comprise any one or more of the following:
- In various aspects, such an inventive complex can comprise any one or more of the following:
- In one aspect, a complex disclosed herein can have the structure:
- wherein each A independently is O, S, NR, PR, AsR, CR2, SiR2, or BR,
wherein each U independently is O S, NR, PR, AsR, CR2, SiR2, or BR,
wherein M is Pt or Pd, and -
- is any one of
- In one aspect, a disclosed complex can have the structure:
- wherein each A independently is O, S, NR, PR, AsR, CR2, SiR2, or BR,
- wherein each U independently is O S, NR, PR, AsR, CR2, SiR2, or BR,
wherein M is Mn or Ni, and
where - is any one of
- In one aspect, a disclosed complex can have the structure:
- wherein each A independently is O, S, NR, PR, AsR, CR2, SiR2, or BR,
wherein each U independently is O S, NR, PR, AsR, CR2, SiR2, or BR,
wherein M is Ir, Rh, or Cu, and
wherein - is any one of
- In one aspect, a disclosed compound can have the structure:
- wherein each A independently is O, S, NR, PR, AsR, CR2, SiR2, or BR,
- wherein each U independently is O S, NR, PR, AsR, CR2, SiR2, or BR,
- wherein M is Au or Ag, and
- wherein
- is any one of
- In one aspect, a disclosed complex can have the structure:
- FL groups are covalently bonded to any component of metal complexes including the Ar1 group.
- wherein each A independently is O, S, NR, PR, AsR, CR2, SiR2, BR, or BR2,
- wherein each U independently is O S, NR, PR, AsR, CR2, SiR2, or BR,
- wherein X is C or N,
- wherein M is Pd, Mn, Ni, Ir, Rh, Cu, Au, or Ag,
- wherein FL is any one of
- wherein FL is covalently bonded to any component of the complex, for example, the Ar1 group;
- wherein
- is any one of
- In one aspect, the FL group is covalently bonded to the Ar1 group.
- In one aspect, any one or more of the compounds disclosed herein can be excluded from the present invention.
- The inventive complexes described herein can be prepared according to methods such as those provide in the Examples or that one of skill in the art, in possession of this disclosure, could readily discern from this disclosure and from methods known in the art.
- Also disclosed herein is a device comprising one or more of the disclosed complexes or compounds. As briefly described above, the present invention is directed to metal complexes. In one aspect, the compositions disclosed here can be used as host materials for OLED applications, such as full color displays.
- The organic light emitting diodes with metal-assisted delayed fluorescent emitters can have the potential of harvesting both electrogenerated singlet and triplet excitons and achieving 100% internal quantum efficiency in the device settings. The component of delayed fluorescence process will occurred at a higher energy than that of phosphorescence process, which can provide a blue-shifted emission spectrum than those originated exclusively from the lowest triplet excited state of metal complexes. On the other hand, the existence of metal ions (especially the heavy metal ions) will facilitate the phosphorescent emission inside of the emitters, ensuring a high emission quantum efficiency.
- The energy of the singlet excited states of metal-assisted delayed fluorescent emitters can be adjusted separately from the lowest triplet excited by ether modifying the energy of donor-accepter ligands or attaching fluorescent emitters which are covalently bonded to metal complexes without having effective conjugation between fluorescent emitters and metal complexes.
- The inventive compositions of the present disclosure can be useful in a wide variety of applications, such as, for example, lighting devices. In a particular aspect, one or more of the complexes can be useful as host materials for an organic light emitting display device.
- The compounds of the invention are useful in a variety of applications. As light emitting materials, the compounds can be useful in organic light emitting diodes (OLED)s, luminescent devices and displays, and other light emitting devices.
- The energy profile of the compounds can be tuned by varying the structure of the ligand surrounding the metal center. For example, compounds having a ligand with electron withdrawing substituents will generally exhibit different properties, than compounds having a ligand with electron donating substituents. Generally, a chemical structural change affects the electronic structure of the compound, which thereby affects the electrical transport and transfer functions of the material. Thus, the compounds of the present invention can be tailored or tuned to a specific application that desires an energy or transport characteristic.
- In another aspect, the inventive compositions can provide improved efficiency and/or operational lifetimes in lighting devices, such as, for example, organic light emitting devices, as compared to conventional materials.
- In other various aspects, the inventive compositions can be useful as, for example, host materials for organic light emitting diodes, lighting applications, and combinations thereof.
- In one aspect, the compound in the device is selected to have 100% internal quantum efficiency in the device settings.
- In one aspect, the device is an organic light emitting diode. In another aspect, the device is a full color display. In yet another aspect, the device is an organic solid state lighting
- In one embodiment, the compounds can be used in an OLED.
FIG. 1 shows a cross-sectional view of anOLED 100, which includessubstrate 102 with an anode 104, which is typically a transparent material, such as indium tin oxide, a layer of hole-transporting material(s) (HTL) 106, a layer oflight processing material 108, such as an emissive material (EML) including an emitter and a host, a layer of electron-transporting material(s) (ETL) 110, and a metal cathode layer 112. - In one aspect, a light emitting device, such as, for example, an OLED, can comprise one or more layers. In various aspects, any of the one or more layers can comprise indium tin oxide (ITO), poly(3,4-ethylenedioxythiophene) (PEDOT), polystyrene sulfonate (PSS), N,N′-di-1-naphthyl-N,N′-diphenyl-1,1′-biphenyl-4,4′diamine (NPD), 1,1-bis((di-4-tolylamino)phenyl) cyclohexane (TAPC), 2,6-Bis(N-carbazolyl)pyridine (mCpy), 2,8-bis(diphenylphosphoryl)dibenzothiophene (PO15), LiF, Al, or a combination thereof. In another aspect, any of the one or more layers can comprise a material not specifically recited herein.
- In this embodiment, the layer of
light processing material 108 can comprise one or more compounds of the present invention optionally together with a host material. The host material can be any suitable host material known in the art. The emission color of an OLED is determined by the emission energy (optical energy gap) of thelight processing material 108, which as discussed above can be tuned by tuning the electronic structure of the emitting compounds and/or the host material. Both the hole-transporting material in theHTL layer 106 and the electron-transporting material(s) in theETL layer 110 can comprise any suitable hole-transporter known in the art. A selection of which is well within the purview of those skilled in the art. - It will be apparent that the compounds of the present invention can, in various aspects, exhibit phosphorescence. Phosphorescent OLEDs (i.e., OLEDs with phosphorescent emitters) typically have higher device efficiencies than other OLEDs, such as fluorescent OLEDs. Light emitting devices based on electrophosphorescent emitters are described in more detail in WO2000/070655 to Baldo et al., which is incorporated herein by this reference for its teaching of OLEDs, and in particular phosphorescent OLEDs.
- The compounds of the invention can be made using a variety of methods, including, but not limited to those recited in the examples provided herein. In other aspects, one of skill in the art, in possession of this disclosure, could readily determine an appropriate method for the preparation of an iridium complex as recited herein.
- The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how the compounds, compositions, articles, devices and/or methods claimed herein are made and evaluated, and are intended to be purely exemplary of the invention and are not intended to limit the scope of what the inventors regard as their invention. Efforts have been made to ensure accuracy with respect to numbers (e.g., amounts, temperature, etc.), but some errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, temperature is in ° C. or is at ambient temperature, and pressure is at or near atmospheric.
- Hereinafter, the preparation method of the compounds for the displays and lighting applications will be illustrated. However, the following embodiments are only exemplary and do not limit the scope of the present invention. Temperatures, catalysts, concentrations, reactant compositions, and other process conditions can vary, and one of skill in the art, in possession of this disclosure, could readily select appropriate reactants and conditions for a desired complex.
- In one aspect, a PdN3N complex can be prepared based on the following examples.
-
- Under a nitrogen atmosphere, 20 mL of water was heated to 60° C. and 125 mmol of 2-nitrobyphenyl was added and stirred for 30 minutes before 6.3 mmol of iron trichloride was added and stirred for 30 minutes further. 140 mmol was added drop wise over 40 minutes and allowed to stir overnight before setting to reflux for 4 hours. After cooling, residual bromine was removed by washing with a sodium bisulfate solution. The organic residue was then washed with concentrated sodium hydroxide, and then twice with water. The organic portion was separated and dissolved in dichloromethane before being dried with magnesium sulfate. The solution was concentrated under reduced pressure, subjected to flash column chromatography of silica with dichloromethane as the eluent, and concentrated again under reduced pressure. 4′-bromo-2-nitrobiphenyl was collected by recrystallization from methanol in 50% yield.
-
- Under a nitrogen atmosphere, 100 mmol of 4′-bromo-2-nitrobiphenyl was set to reflux overnight in stirring tirethylphosphite. After cooling, the triethylphosphite was distilled off and 2-bromo-9H-carbazole was isolated by recrystallization from methanol and further purified by train sublimation, resulting in a 65% yield.
-
- Under a nitrogen atmosphere, 10 mmol of 2-bromo-9H-carbazole, 10 mmol of 2-bromopyridine, 1 mmol of copper(I)iodide, 25 mmol of potassium carbonate, and 2 mmol of L-proline were combined in stirring degassed dimethyl sulfoxide. The mixture was heated to 90° C. for 3 days before being cooled and separated between dichloromethane and water. The water layer was washed twice with dichloromethane and the organics were combined and washed once with brine. The organic fraction was dried with magnesium sulfate and concentrated under reduced pressure and subjected to column chromatography of silica with dichloromethane as the eluent. After concentrating under reduced pressure, 2-bromo-9-(pyridin-2-yl)-9H-carbazole was isolated in a 70% yield.
-
- A vessel was charged with 5
mmol 4′-bromo-2-nitrobiphenyl, 12.5 mmol 2-(tributylstannyl)pyridine, 0.25 mmol tetrakistriphenylphosphine palladium(0), 20 mmol potassium fluoride, and 75 mL anhydrous, degassed toluene. The vessel was set to reflux under a nitrogen atmosphere for 3 days. The resulting solution was cooled, the solids filtered off, and poured into a stirring aqueous solution of potassium fluoride. The organic phase was collected, washed once more with aqueous potassium fluoride, and dried of magnesium sulfate. The solvent was removed under reduced pressure and the crude product was chromatographed over silica initially with hexane followed by dichloromethane to yield a viscous, colorless oil in 60% yield. - Under a nitrogen atmosphere, 100 mmol of 2-[4-(2-nitrophenyl)phenyl]pyridine was set to reflux overnight in stirring tirethylphosphite. After cooling, the triethylphosphite was distilled off, the solids dissolved in
- dichloromethane, and rinsed three times with water. The organic fraction was dried with magnesium sulfate and concentrated under reduced pressure and subjected to column chromatography of silica with dichloromethane as the eluent. After concentrating under reduced pressure, 2-(2-pyridyl)-9H-carbazole was isolated in a 60% yield.
-
- Under a nitrogen atmosphere, 10 mmol of 2-(2-pyridyl)-9H-carbazole, 10 mmol of 2-bromo-9-(pyridin-2-yl)-9H-carbazole, 1 mmol of copper(I)iodide, 25 mmol of potassium carbonate, and 2 mmol of L-proline were combined in stirring degassed dimethyl sulfoxide. The mixture was heated to 90° C. for 3 days before being cooled and separated between dichloromethane and water. The water layer was washed twice with dichloromethane and the organics were combined and washed once with brine. The organic fraction was dried with magnesium sulfate and concentrated under reduced pressure and subjected to column chromatography of silica with dichloromethane/ethyl acetate as the eluent. After concentrating under reduced pressure, 2-(2-pyridyl)-9-[9-(2-pyridyl)carbazol-2-yl]carbazole was isolated in a 60% yield.
-
- Under a nitrogen atmosphere, 10 mmol of 2-(2-pyridyl)-9-[9-(2-pyridyl)carbazol-2-yl]carbazole, 9 mmol of PdCl2, and 4{acute over (Å)} molecular sieves were added to stirring acetic acid. The mixture was stirred at room temperature overnight, heated to 60° C. for 3 days, then to 90° C. for 3 days. The solution was cooled, and poured into 100 mL of stirring dichloromethane. The mixture was filtered, and the filtrate concentrated under reduced pressure. The solid was subjected to flash chromatography of alumina with dichloromethane as the eluent and isolate in 20% yield.
-
- To a solution of substrate (247 mg) in HOAc (26 mL) were added Pd(OAc)2 (123 mg) and n-Bu4NBr (17 mg). The mixture was heated to reflux for 3 days. The reaction mixture was cooled to rt, filtered through a pad of silica gel, and concentrated. Purification by column chromatography (hexanes:DCM=1:1 to 1:2) gave PdN1N (121 mg, yield: 40%). 1H NMR (400 MHz, DMSO-d6) δ 9.05 (d, J=5.6 Hz, 1H), 8.91 (d, J=2.6 Hz, 1H), 8.29-8.09 (m, 7H), 8.09-7.98 (m, 3H), 7.71 (d, J=8.2 Hz, 1H), 7.55-7.45 (m, 3H), 7.41 (t, J=7.5 Hz, 1H), 7.30 (t, J=7.5 Hz, 1H), 6.79 (t, J=2.5 Hz, 1H).
-
- To a solution of substrate (827 mg) in HOAc (75 mL) were added Pd(OAc)2 (354 mg) and n-Bu4NBr (48 mg). The mixture was heated to reflux for 3 days. The reaction mixture was cooled to rt, filtered through a pad of silica gel, and concentrated. Purification by column chromatography (hexanes:DCM=1:1 to 1:2) gave PdN6N (463 mg, yield: 47%). 1H NMR (400 MHz, DMSO-d6) δ 9.42 (s, 1H), 9.13 (d, J=5.5 Hz, 1H), 8.61 (s, 1H), 8.30-8.12 (m, 6H), 8.10-8.02 (m, 3H), 7.89 (d, J=7.6 Hz, 2H), 7.74 (d, J=8.2 Hz, 1H), 7.57-7.45 (m, 5H), 7.42 (t, J=7.5 Hz, 1H), 7.36-7.28 (m, 2H).
-
- To a solution of substrate (243 mg) in HOAc (21 mL) were added Pd(OAc)2 (99 mg) and n-Bu4NBr (14 mg). The mixture was heated to reflux for 24 hours. The reaction mixture was cooled to rt, filtered through a pad of silica gel, and concentrated. Purification by column chromatography (hexanes:DCM=1:1 to 1:2) gave the product (216 mg, yield: 75%). 1H NMR (400 MHz, DMSO-d6) δ 9.05 (d, J=5.5 Hz, 1H), 8.63 (d, J=5.5 Hz, 1H), 8.21-8.11 (m, 3H), 8.07 (d, J=8.2 Hz, 1H), 7.90 (d, J=8.2 Hz, 1H), 7.86 (d, J=7.8 Hz, 2H), 7.83-7.75 (m, 3H), 7.63 (d, J=7.8 Hz, 2H), 7.57-7.36 (m, 7H), 7.31 (t, J=7.6 Hz, 1H), 7.22 (d, J=8.2 Hz, 1H), 7.18 (d, J=7.9 Hz, 1H), 2.68 (s, 3H).
-
- To a solution of substrate (178 mg) in HOAc (15 mL) were added Pd(OAc)2 (71 mg) and n-Bu4NBr (10 mg). The mixture was heated to reflux for 24 hours. The reaction mixture was cooled to rt, filtered through a pad of silica gel, and concentrated. Purification by column chromatography (hexanes:DCM=1:1 to 1:2) gave the product (162 mg, yield: 77%). 1H NMR (500 MHz, DMSO-d6) δ 8.99 (d, J=4.4 Hz, 1H), 8.70 (d, J=4.4 Hz, 1H), 8.34 (d, J=8.3 Hz, 1H), 8.22-8.13 (m, 3H), 8.12-8.04 (m, 2H), 7.93 (d, J=8.3 Hz, 1H), 7.72 (d, J=7.2 Hz, 2H), 7.60 (s, 1H), 7.57 (t, J=6.0 Hz, 1H), 7.53-7.44 (m, 6H), 7.43-7.35 (m, 2H), 7.23 (d, J=8.2 Hz, 1H), 6.94 (d, J=1.5 Hz, 1H), 2.19 (s, 6H).
-
- To a solution of substrate (154 mg) in HOAc (13 mL) were added Pd(OAc)2 (61 mg) and n-Bu4NBr (9 mg). The mixture was heated to reflux for 24 hours. The reaction mixture was cooled to rt, filtered through a pad of silica gel, and concentrated. Purification by column chromatography (hexanes:DCM=1:1 to 1:2) gave the product (153 mg, yield: 84%). 1H NMR (400 MHz, DMSO-d6) δ 9.07 (d, J=5.5 Hz, 1H), 8.73 (d, J=5.5 Hz, 1H), 8.22-8.11 (m, 4H), 8.06 (d, J=8.3 Hz, 1H), 7.92 (d, J=8.3 Hz, 1H), 7.83 (d, J=7.5 Hz, 1H), 7.72 (d, J=7.1 Hz, 2H), 7.55-7.36 (m, 9H), 7.27-7.20 (m, 2H), 7.16 (d, J=8.0 Hz, 1H), 2.19 (s, 6H).
Claims (22)
1. A metal-assisted delayed fluorescent emitter represented by one or more of formulas
wherein A is an accepting group comprising one or more of the following structures, which can optionally be substituted
wherein D is a donor group comprising one or more of the following structures,
which can optionally be substituted,
wherein C in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
wherein N in structure (a) or (b) comprises one or more of the following structures, which can optionally be substituted
a direct bond and/or linking group comprising one or more of the following,
wherein b1 and b2 independently is present or absent, and if present, comprises a linking group comprising one or more of the following
wherein X is B, C, N, O, Si, P, S, Ge, As, Se, Sn, Sb, or Te,
wherein Y is O, S, S═O, SO2, Se, N, NR3, PR3, RP═O, CR1R2, C═O, SiR1R2, GeR1R2, BH, P(O)H, PH, NH, CR1H, CH2, SiH2, SiHR1, BH, or BR3,
wherein each of R, R1, R2, and R3 independently is hydrogen, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, a mono- or di-alkylamino, a mono- or diaryl amino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureidc, phosphoramide, amercapto, sulfo, carboxyl, hydrzino, substituted silyl, or polymerizable, or any conjugate or combination thereof,
wherein n is a number that satisfies the valency of Y,
wherein M is platinum (II), palladium (II), nickel (I), manganese (II), zinc (II), gold (III), silver (III), copper (III), iridium (I), rhodium (I), and/or cobalt (I).
2. The metal-assisted delayed fluorescent emitter of claim 1 , wherein a2 is absent in structure A.
3. The metal-assisted delayed fluorescent emitter of claim 1 , wherein a2 and b2 are absent.
4. The metal-assisted delayed fluorescent emitter of claim 1 , wherein X is N.
8. The metal-assisted delayed fluorescent emitter of claim 1 , wherein M is Palladium (II).
10. A metal-assisted delayed fluorescent emitter having the structure
wherein M comprises Ir, Rh, Mn, Ni, Cu, or Ag;
wherein each of R1 and R2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
wherein each of Y2a, Y2b, Y2c, and Y2d independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
each of Y3a, Y3b, Y3c, Y3d, Y4a, Y4b, Y4c, and Y4d independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of m and n independently are an integer 1 or 2;
11. The metal-assisted delayed fluorescent emitter of claim 10 , wherein Y2b is CH, wherein Y2c, Y3b and Y4b is N, wherein M is Ir or Rh.
12. A metal-assisted delayed fluorescent emitter having the structure
wherein M comprises Pt, Pd and Au;
wherein each of R1 and R2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
wherein each of Y2a, Y2b, Y2c, and Y2d independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
each of Y3a, Y3b, Y3c, Y3d, Y3e, Y3f, Y4a, Y4b, Y4c, and Y4d independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of m is an integer 1 or 2;
13. The metal-assisted delayed fluorescent emitter of claim 12 , wherein Y2b and Y2c is C, wherein Y3b and Y4b is N, wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
wherein M is Pt or Pd.
14. The metal-assisted delayed fluorescent emitter of claim 12 , wherein Y2b, Y2c and Y4b is CH, wherein Y3b is N, wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure; wherein M is Au.
15. A metal-assisted delayed fluorescent emitter having the structure
wherein M comprises Pt, Pd, Au, Ag;
wherein each of R1 and R2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein one of Y1a and Y1b is B(R2)2 and the other of Y1a and Y1b is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
wherein each of Y2a, Y2b, Y2c, and Y2d independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
each of Y3a, Y3b, Y3c, Y3d, Y4a, Y4b, Y4c, and Y4d independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of in and n independently are an integer 1 or 2;
16. A metal-assisted delayed fluorescent emitter having the structure:
wherein M comprises Ir, Rh, Pt, Os, Zr, Co, or Ru;
wherein each of R1 and R2 independently are hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, nitro hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of Y1a, Y1b, Y1c and Y1d independently is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
wherein Y1e is O, NR2, CR2R3, S, AsR2, BR2, PR2, P(O)R2, or SiR2R3, or a combination thereof, or nothing, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloakane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
wherein each of Y2a, Y2b, Y2c, and Y2d independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of Y3a, Y3b, Y3c, Y3d, Y3e, Y4a, Y4b, Y4c, and Y4d independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein in each of each of Y5a, Y5b, Y5c, Y5d, Y6a, Y6b, Y6c, and Y6d independently is N, O, S, NR6a, or CR6b;
wherein each of m, n, l and p independently are an integer 1 or 2;
17. A metal-assisted delayed fluorescent emitter having the structure
wherein M comprises Pd, Ir, Rh, Au, Co, Mn, Ni, Ag, or Cu;
wherein each of Y1a and Y1b independently is O, NR2, CR2R3, S, AsR2, BR2, B(R2)2,PR2, P(O)R2, or SiR2R3, or a combination thereof, wherein each of R2 and R3 independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, arylalkene, or R2 and R3 together form C═O, wherein each of R2 and R3 independently is optionally linked to an adjacent ring structure, thereby forming a cyclic structure;
wherein each of Y2a, Y2b, Y2c, Y2d, Y2e, Y2f, Y2g, and Y2h independently is N, NR6a, or CR6b, wherein each of R6a and R6b independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
each of Y3a, Y3b, Y3c, Y3d, Y3eY4a, Y4b, Y4c, Y4d and Y4e independently is N, O, S, NR6a, CR6b, wherein each of R6a and R6b independently hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocycyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene; or Z(R6c)2, wherein Z is C or Si, and wherein each R6c independently is hydrogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkane, cycloalkane, heterocyclyl, amino, hydroxyl, halogen, thio, alkoxy, haloalkyl, arylalkane, or arylalkene;
wherein each of m is the integer 1 or 2;
wherein each of n is the integer 1 or 2;
wherein each of Fl1, Fl2, Fl3 and Fl4 independently are fluorescent emitters with tunable singlet excited state energies which are covenantly bonded to selected atoms among Y2a, Y2d, Y2e, Y2f, Y2g, Y2h, Y3c, Y3d, Y3eY4c, Y4d and Y4e.
18. A metal-assisted delayed fluorescent emitter, having a singlet excited state/states energy from 0 to 0.2 eV higher than a lowest triplet state energy, and being capable of emitting simultaneously from the lowest triplet state and the singlet excited state/states at room temperature or elevated temperature and harvesting both electrogenerated singlet and triplet excitons.
19. A device comprising the metal-assisted delayed fluorescent emitter of claim 1 .
20. The device of claim 19 , wherein the metal-assisted delayed fluorescent emitter is selected to have 100% internal quantum efficiency in the device settings.
21. The device of claim 19 , wherein the device is an organic light emitting diode.
22. The device of claim 19 , wherein the device is a fall color display.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/437,963 US20150274762A1 (en) | 2012-10-26 | 2013-10-25 | Metal complexes, methods, and uses thereof |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261719077P | 2012-10-26 | 2012-10-26 | |
US14/437,963 US20150274762A1 (en) | 2012-10-26 | 2013-10-25 | Metal complexes, methods, and uses thereof |
PCT/US2013/066793 WO2014109814A2 (en) | 2012-10-26 | 2013-10-25 | Metal complexes, methods, and uses thereof |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2013/066793 A-371-Of-International WO2014109814A2 (en) | 2012-10-26 | 2013-10-25 | Metal complexes, methods, and uses thereof |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US15/905,385 Continuation US10995108B2 (en) | 2012-10-26 | 2018-02-26 | Metal complexes, methods, and uses thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
US20150274762A1 true US20150274762A1 (en) | 2015-10-01 |
Family
ID=51167489
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/437,963 Abandoned US20150274762A1 (en) | 2012-10-26 | 2013-10-25 | Metal complexes, methods, and uses thereof |
US15/905,385 Active US10995108B2 (en) | 2012-10-26 | 2018-02-26 | Metal complexes, methods, and uses thereof |
US17/212,209 Pending US20210230198A1 (en) | 2012-10-26 | 2021-03-25 | Metal Complexes, Methods, and Uses Thereof |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US15/905,385 Active US10995108B2 (en) | 2012-10-26 | 2018-02-26 | Metal complexes, methods, and uses thereof |
US17/212,209 Pending US20210230198A1 (en) | 2012-10-26 | 2021-03-25 | Metal Complexes, Methods, and Uses Thereof |
Country Status (2)
Country | Link |
---|---|
US (3) | US20150274762A1 (en) |
WO (1) | WO2014109814A2 (en) |
Cited By (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106803543A (en) * | 2017-01-20 | 2017-06-06 | 瑞声科技(南京)有限公司 | Organic light emitting display |
US9711741B2 (en) | 2012-08-24 | 2017-07-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal compounds and methods and uses thereof |
CN106972109A (en) * | 2017-04-21 | 2017-07-21 | 瑞声科技(南京)有限公司 | A kind of luminescent device |
JP2017152585A (en) * | 2016-02-25 | 2017-08-31 | 株式会社ジャパンディスプレイ | Material for organic electroluminescence display device, and organic electroluminescence display device |
US20180145273A1 (en) * | 2014-08-29 | 2018-05-24 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, electronic device, and lighting device |
US10020455B2 (en) | 2014-01-07 | 2018-07-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complex emitters containing phenyl-pyrazole and its analogues |
US10033003B2 (en) | 2014-11-10 | 2018-07-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes with carbon group bridging ligands |
US10056564B2 (en) | 2015-06-02 | 2018-08-21 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes containing indoloacridine and its analogues |
US10158091B2 (en) | 2015-08-04 | 2018-12-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes, devices, and uses thereof |
US10177323B2 (en) | 2016-08-22 | 2019-01-08 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes and octahedral iridium complexes employing azepine functional groups and their analogues |
US10211414B2 (en) | 2013-06-10 | 2019-02-19 | Arizona Board Of Regents On Behalf Of Arizona State University | Phosphorescent tetradentate metal complexes having modified emission spectra |
US10263197B2 (en) | 2010-04-30 | 2019-04-16 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof |
KR20190052552A (en) * | 2017-11-08 | 2019-05-16 | 삼성전자주식회사 | Organometallic compound, organic light emitting device including the same and a composition for diagnosing including the same |
US10297778B2 (en) | 2017-03-06 | 2019-05-21 | Samsung Electronics Co., Ltd. | Light-emitting device |
US10294417B2 (en) | 2014-08-22 | 2019-05-21 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent materials as co-host materials for fluorescent OLEDS |
US10414785B2 (en) | 2011-04-14 | 2019-09-17 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Pyridine-oxyphenyl coordinated iridium (III) complexes and methods of making and using |
US10516117B2 (en) | 2017-05-19 | 2019-12-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emttters employing benzo-imidazo-phenanthridine and analogues |
US10566553B2 (en) | 2013-10-14 | 2020-02-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Platinum complexes and devices |
US10622571B2 (en) | 2012-09-24 | 2020-04-14 | Arizona Board Of Regents For And On Behalf Of Arizona State University | Metal compounds, methods, and uses thereof |
US10790457B2 (en) | 2014-07-29 | 2020-09-29 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emitters containing tridentate ligands |
US10793546B2 (en) | 2014-08-15 | 2020-10-06 | Arizona Board Of Regents On Behalf Of Arizona State University | Non-platinum metal complexes for excimer based single dopant white organic light emitting diodes |
US10804476B2 (en) | 2011-05-26 | 2020-10-13 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University | Synthesis of platinum and palladium complexes as narrow-band phosphorescent emitters for full color displays |
US10822363B2 (en) | 2016-10-12 | 2020-11-03 | Arizona Board Of Regents On Behalf Of Arizona State University | Narrow band red phosphorescent tetradentate platinum (II) complexes |
US10836785B2 (en) | 2015-06-03 | 2020-11-17 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate and octahedral metal complexes containing naphthyridinocarbazole and its analogues |
US10851106B2 (en) | 2017-05-19 | 2020-12-01 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University | Substituted benzo[4,5]imidazo[1,2-F]phenanthridines, dibenzo[I.K]benzo[4,5]imidazo[1,2-F]benzofurophenanthridines and dibenzo[I.K]benzo[4,5]imidazo[1,2-F]benzo[4,5]thienophenanthridines as thermally assisted delayed fluorescent materials |
US10886478B2 (en) | 2014-07-24 | 2021-01-05 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) complexes cyclometalated with functionalized phenyl carbene ligands and their analogues |
US10892427B2 (en) | 2017-05-23 | 2021-01-12 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the organometallic compound, and diagnostic composition including the organometallic compound |
US20210043856A1 (en) * | 2019-08-09 | 2021-02-11 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including organometallic compound, and diagnostic composition including organometallic compound |
US10950807B2 (en) | 2017-04-21 | 2021-03-16 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the organometallic compound, and diagnostic composition including the organometallic compound |
US10964897B2 (en) | 2014-07-28 | 2021-03-30 | Arizona Board Of Regents On Behalf Of Arizona State University | Tridentate cyclometalated metal complexes with six-membered coordination rings |
US10988495B2 (en) | 2017-04-25 | 2021-04-27 | Samsung Electronics Co., Ltd. | Organometallic compound, organic-light emitting device including the same, and diagnostic composition including the organometallic compound |
US10991897B2 (en) | 2014-11-10 | 2021-04-27 | Arizona Board Of Regents On Behalf Of Arizona State University | Emitters based on octahedral metal complexes |
US10995108B2 (en) | 2012-10-26 | 2021-05-04 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal complexes, methods, and uses thereof |
US11011712B2 (en) | 2014-06-02 | 2021-05-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate cyclometalated platinum complexes containing 9,10-dihydroacridine and its analogues |
US11101435B2 (en) | 2017-05-19 | 2021-08-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complexes based on biscarbazole and analogues |
US11183670B2 (en) | 2016-12-16 | 2021-11-23 | Arizona Board Of Regents On Behalf Of Arizona State University | Organic light emitting diode with split emissive layer |
US11245078B2 (en) | 2015-08-25 | 2022-02-08 | Arizona Board Of Regents On Behalf Of Arizona State University | Thermally activated delayed fluorescent material based on 9,10-dihydro-9,9-dimethylacridine analogues for prolonging device longevity |
US11329244B2 (en) | 2014-08-22 | 2022-05-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Organic light-emitting diodes with fluorescent and phosphorescent emitters |
US11335865B2 (en) | 2016-04-15 | 2022-05-17 | Arizona Board Of Regents On Behalf Of Arizona State University | OLED with multi-emissive material layer |
US11450816B2 (en) | 2017-05-19 | 2022-09-20 | Arizona Board Of Regents On Behalf Of Arizona State University | Donor-acceptor type thermally activated delayed fluorescent materials based on imidazo[1,2-f]phenanthridine and analogues |
US11594691B2 (en) | 2019-01-25 | 2023-02-28 | Arizona Board Of Regents On Behalf Of Arizona State University | Light outcoupling efficiency of phosphorescent OLEDs by mixing horizontally aligned fluorescent emitters |
US11594688B2 (en) | 2017-10-17 | 2023-02-28 | Arizona Board Of Regents On Behalf Of Arizona State University | Display and lighting devices comprising phosphorescent excimers with preferred molecular orientation as monochromatic emitters |
US11647643B2 (en) | 2017-10-17 | 2023-05-09 | Arizona Board Of Regents On Behalf Of Arizona State University | Hole-blocking materials for organic light emitting diodes |
US11708385B2 (en) | 2017-01-27 | 2023-07-25 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emitters employing pyrido-pyrrolo-acridine and analogues |
US11785838B2 (en) | 2019-10-02 | 2023-10-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Green and red organic light-emitting diodes employing excimer emitters |
US11839143B2 (en) | 2019-07-02 | 2023-12-05 | Samsung Display Co., Ltd. | Organometallic compound and organic light-emitting device including same |
US11878988B2 (en) | 2019-01-24 | 2024-01-23 | Arizona Board Of Regents On Behalf Of Arizona State University | Blue phosphorescent emitters employing functionalized imidazophenthridine and analogues |
US11925104B2 (en) | 2017-07-21 | 2024-03-05 | Samsung Display Co., Ltd. | Organometallic compound and organic light-emitting device including the same |
US11930662B2 (en) | 2015-06-04 | 2024-03-12 | Arizona Board Of Regents On Behalf Of Arizona State University | Transparent electroluminescent devices with controlled one-side emissive displays |
US11945985B2 (en) | 2020-05-19 | 2024-04-02 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal assisted delayed fluorescent emitters for organic light-emitting diodes |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101792266B1 (en) | 2009-04-06 | 2017-10-31 | 아리조나 보드 오브 리전트스, 아리조나주의 아리조나 주립대 대행법인 | Synthesis of four coordinated platinum complexes and their applications in light emitting devices thereof |
DE112011101527T5 (en) | 2010-04-30 | 2013-05-16 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Synthesis of four-coordinate gold complexes and their applications in light-emitting devices |
US8816080B2 (en) | 2011-02-18 | 2014-08-26 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Four coordinated platinum and palladium complexes with geometrically distorted charge transfer state and their applications in light emitting devices |
US9224963B2 (en) | 2013-12-09 | 2015-12-29 | Arizona Board Of Regents On Behalf Of Arizona State University | Stable emitters |
WO2015091716A1 (en) | 2013-12-20 | 2015-06-25 | Basf Se | Highly efficient oled devices with very short decay times |
US10056567B2 (en) | 2014-02-28 | 2018-08-21 | Arizona Board Of Regents On Behalf Of Arizona State University | Chiral metal complexes as emitters for organic polarized electroluminescent devices |
CN104211634A (en) * | 2014-07-23 | 2014-12-17 | 常州创索新材料科技有限公司 | Synthetic method of 2-bromocarbazole |
WO2016088354A1 (en) * | 2014-12-05 | 2016-06-09 | 出光興産株式会社 | Metal complex compound, material for organic electroluminescent element, composition, organic electroluminescent element, and electronic device |
EP3304612B1 (en) | 2015-06-03 | 2022-05-04 | UDC Ireland Limited | Highly efficient oled devices with very short decay times |
CN105061296B (en) * | 2015-08-10 | 2018-02-06 | 张家港江苏科技大学产业技术研究院 | A kind of preparation method of 2 substituted carbazole class compound |
EP3133078B1 (en) * | 2015-08-18 | 2019-01-30 | Samsung Electronics Co., Ltd. | Organometallic compound and organic light-emitting device including the same |
US10236456B2 (en) | 2016-04-11 | 2019-03-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
TW202030902A (en) | 2018-09-12 | 2020-08-16 | 德商麥克專利有限公司 | Electroluminescent devices |
TWI826522B (en) | 2018-09-12 | 2023-12-21 | 德商麥克專利有限公司 | Electroluminescent devices |
US20220127286A1 (en) | 2019-03-04 | 2022-04-28 | Merck Patent Gmbh | Ligands for nano-sized materials |
US20200321537A1 (en) * | 2019-03-29 | 2020-10-08 | Samsung Electronics Co., Ltd. | Organic light-emitting device |
WO2021003417A1 (en) | 2019-07-03 | 2021-01-07 | Sumitomo Dainippon Pharma Oncology, Inc. | Tyrosine kinase non-receptor 1 (tnk1) inhibitors and uses thereof |
CN115052865A (en) | 2020-01-29 | 2022-09-13 | 默克专利有限公司 | Benzimidazole derivatives |
CN111205273A (en) * | 2020-03-02 | 2020-05-29 | 南京工业大学 | Bivalent platinum complex and preparation method and application thereof |
US20220271241A1 (en) * | 2021-02-03 | 2022-08-25 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP4347610A1 (en) * | 2021-05-31 | 2024-04-10 | Versitech Limited | Thermally activated delayed fluorescent palladium (ii) complexes for oled applications |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9238668B2 (en) * | 2011-05-26 | 2016-01-19 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University | Synthesis of platinum and palladium complexes as narrow-band phosphorescent emitters for full color displays |
Family Cites Families (237)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53120687A (en) | 1977-03-30 | 1978-10-21 | Taki Chem Co Ltd | Hardener |
US4769292A (en) | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
DE69017039T2 (en) | 1989-11-08 | 1995-07-20 | British Tech Group | GAS SENSOR AND CONNECTIONS SUITABLE FOR THIS. |
US5641878A (en) | 1991-05-15 | 1997-06-24 | Diatron Corporation | Porphyrin, azaporphyrin, and related fluorescent dyes free of aggregation and serum binding |
US5707745A (en) | 1994-12-13 | 1998-01-13 | The Trustees Of Princeton University | Multicolor organic light emitting devices |
US5844363A (en) | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
JP4142782B2 (en) | 1998-06-26 | 2008-09-03 | Tdk株式会社 | Organic EL device |
EP1729327B2 (en) | 1999-05-13 | 2022-08-10 | The Trustees Of Princeton University | Use of a phosphorescent iridium compound as emissive molecule in an organic light emitting device |
US6821645B2 (en) | 1999-12-27 | 2004-11-23 | Fuji Photo Film Co., Ltd. | Light-emitting material comprising orthometalated iridium complex, light-emitting device, high efficiency red light-emitting device, and novel iridium complex |
JP4154140B2 (en) | 2000-09-26 | 2008-09-24 | キヤノン株式会社 | Metal coordination compounds |
JP4460743B2 (en) | 2000-09-29 | 2010-05-12 | 富士フイルム株式会社 | Method for producing iridium complex or tautomer thereof |
EP2272485A3 (en) | 2001-08-15 | 2014-07-16 | 3M Innovative Properties Co. | Hardenable self-supporting structures and methods |
JP4166455B2 (en) | 2001-10-01 | 2008-10-15 | 株式会社半導体エネルギー研究所 | Polarizing film and light emitting device |
US20030186077A1 (en) | 2001-12-31 | 2003-10-02 | Chen Jian P. | Bis- and tris- (di) benzocarbazole-based materials as hole transport materials for organic light emitting devices |
JP2003342284A (en) | 2002-05-30 | 2003-12-03 | Canon Inc | Metal coordination compound, light-generating element and display device |
GB0215153D0 (en) | 2002-07-01 | 2002-08-07 | Univ Hull | Luminescent compositions |
DE10238903A1 (en) | 2002-08-24 | 2004-03-04 | Covion Organic Semiconductors Gmbh | New heteroaromatic rhodium and iridium complexes, useful in electroluminescent and/or phosphorescent devices as the emission layer and for use in solar cells, photovoltaic devices and organic photodetectors |
EP1577300A1 (en) | 2002-11-01 | 2005-09-21 | Takasago International Corporation | Platinum complexes |
US7037599B2 (en) | 2003-02-28 | 2006-05-02 | Eastman Kodak Company | Organic light emitting diodes for production of polarized light |
KR101391117B1 (en) | 2003-03-24 | 2014-04-30 | 유니버시티 오브 써던 캘리포니아 | Phenyl-pyrazole complexes of ir |
US6998492B2 (en) | 2003-05-16 | 2006-02-14 | Semiconductor Energy Laboratory Co., Ltd. | Organometallic complex and light-emitting element containing the same |
WO2004108857A1 (en) | 2003-06-02 | 2004-12-16 | Fuji Photo Film Co., Ltd. | Organic electroluminescent devices and metal complex compounds |
JP4460952B2 (en) | 2003-06-02 | 2010-05-12 | 富士フイルム株式会社 | Organic electroluminescent device and complex compound |
CN100551994C (en) | 2003-06-02 | 2009-10-21 | 富士胶片株式会社 | Organnic electroluminescent device and metal complex compounds |
US6917159B2 (en) | 2003-08-14 | 2005-07-12 | Eastman Kodak Company | Microcavity OLED device |
US7268485B2 (en) | 2003-10-07 | 2007-09-11 | Eastman Kodak Company | White-emitting microcavity OLED device |
DE10350722A1 (en) | 2003-10-30 | 2005-05-25 | Covion Organic Semiconductors Gmbh | metal complexes |
WO2005042444A2 (en) | 2003-11-04 | 2005-05-12 | Takasago Perfumery Co Ltd | Platinum complex and luminescent element |
US7332232B2 (en) | 2004-02-03 | 2008-02-19 | Universal Display Corporation | OLEDs utilizing multidentate ligand systems |
JP2005267557A (en) | 2004-03-22 | 2005-09-29 | Ntt Docomo Inc | Server device |
US20050211974A1 (en) | 2004-03-26 | 2005-09-29 | Thompson Mark E | Organic photosensitive devices |
US7445855B2 (en) | 2004-05-18 | 2008-11-04 | The University Of Southern California | Cationic metal-carbene complexes |
WO2005113704A2 (en) | 2004-05-18 | 2005-12-01 | The University Of Southern California | Luminescent compounds with carbene ligands |
US7279704B2 (en) | 2004-05-18 | 2007-10-09 | The University Of Southern California | Complexes with tridentate ligands |
US7393599B2 (en) | 2004-05-18 | 2008-07-01 | The University Of Southern California | Luminescent compounds with carbene ligands |
KR20060011537A (en) | 2004-07-30 | 2006-02-03 | 주식회사 하이닉스반도체 | Method for isolation in semiconductor device |
JP4576605B2 (en) | 2004-08-09 | 2010-11-10 | 独立行政法人産業技術総合研究所 | Identification method of oligosaccharide |
JP4500735B2 (en) | 2004-09-22 | 2010-07-14 | 富士フイルム株式会社 | Organic electroluminescence device |
US7002013B1 (en) | 2004-09-23 | 2006-02-21 | National Tsing Hua University | Pt complexes as phosphorescent emitters in the fabrication of organic light emitting diodes |
JP4531509B2 (en) | 2004-09-27 | 2010-08-25 | 富士フイルム株式会社 | Light emitting element |
US7489074B2 (en) | 2004-09-28 | 2009-02-10 | Osram Opto Semiconductors Gmbh | Reducing or eliminating color change for microcavity OLED devices |
KR101269497B1 (en) | 2004-12-23 | 2013-05-31 | 시바 홀딩 인크 | Electroluminescent metal complexes with nucleophilic carbene ligands |
CN100348594C (en) | 2005-01-12 | 2007-11-14 | 武汉大学 | Bidentate ligand and its iridium complex and electroluminescent device therewith |
JP4773109B2 (en) | 2005-02-28 | 2011-09-14 | 高砂香料工業株式会社 | Platinum complex and light emitting device |
JP4425816B2 (en) | 2005-03-02 | 2010-03-03 | 富士重工業株式会社 | Electronically controlled throttle device |
JP2006242080A (en) | 2005-03-02 | 2006-09-14 | Denso Corp | Abnormality diagnostic device for exhaust gas recirculating device |
JP4399382B2 (en) | 2005-03-16 | 2010-01-13 | 富士フイルム株式会社 | Organic electroluminescence device |
EP2530760A1 (en) | 2005-03-16 | 2012-12-05 | Fujifilm Corporation | Platinum-complex-compound containing organic electroluminescent device |
JP4727262B2 (en) | 2005-03-16 | 2011-07-20 | 富士フイルム株式会社 | Organic electroluminescence device |
JP4399429B2 (en) | 2005-03-16 | 2010-01-13 | 富士フイルム株式会社 | Organic electroluminescence device |
CN101176218A (en) | 2005-04-07 | 2008-05-07 | 加利福尼亚大学董事会 | Highly efficient polymer solar cell by polymer self-organization |
JP4790298B2 (en) | 2005-04-08 | 2011-10-12 | 日本放送協会 | Good solubility iridium complex and organic EL device |
JP5046548B2 (en) | 2005-04-25 | 2012-10-10 | 富士フイルム株式会社 | Organic electroluminescence device |
TWI418606B (en) | 2005-04-25 | 2013-12-11 | Udc Ireland Ltd | Organic electroluminescent device |
JP4934346B2 (en) | 2005-04-25 | 2012-05-16 | 富士フイルム株式会社 | Organic electroluminescence device |
JP2006303394A (en) | 2005-04-25 | 2006-11-02 | Fuji Photo Film Co Ltd | Organic electroluminescent element |
US7758971B2 (en) * | 2005-04-25 | 2010-07-20 | Fujifilm Corporation | Organic electroluminescent device |
TWI391027B (en) | 2005-04-25 | 2013-03-21 | Fujifilm Corp | Organic electroluminescent device |
JP4533796B2 (en) | 2005-05-06 | 2010-09-01 | 富士フイルム株式会社 | Organic electroluminescence device |
JP2006351638A (en) | 2005-06-13 | 2006-12-28 | Fujifilm Holdings Corp | Light emitting device |
JP2007031678A (en) | 2005-07-29 | 2007-02-08 | Showa Denko Kk | Polymeric luminescent material and organic electroluminescence element using the polymeric luminescent material |
JP2007042875A (en) | 2005-08-03 | 2007-02-15 | Fujifilm Holdings Corp | Organic electroluminescence element |
JP4796802B2 (en) | 2005-08-15 | 2011-10-19 | 富士フイルム株式会社 | Organic electroluminescence device |
JP4923478B2 (en) | 2005-08-19 | 2012-04-25 | コニカミノルタホールディングス株式会社 | Organic electroluminescence element, display device and lighting device |
JP2007066581A (en) | 2005-08-29 | 2007-03-15 | Fujifilm Holdings Corp | Organic electroluminescent element |
JP5151481B2 (en) | 2005-09-01 | 2013-02-27 | コニカミノルタホールディングス株式会社 | Organic electroluminescence element, display device and lighting device |
JP2007073620A (en) | 2005-09-05 | 2007-03-22 | Fujifilm Corp | Organic electroluminescent element |
US8133597B2 (en) | 2005-09-06 | 2012-03-13 | Konica Minolta Holdings, Inc. | Organic electroluminescent device, display and illuminating device |
JP2007073845A (en) | 2005-09-08 | 2007-03-22 | Fujifilm Holdings Corp | Organic laser oscillator |
JP2007073900A (en) | 2005-09-09 | 2007-03-22 | Fujifilm Corp | Organic electroluminescent element |
JP2007080593A (en) | 2005-09-12 | 2007-03-29 | Fujifilm Corp | Electrochemical light-emitting element |
JP2007110067A (en) | 2005-09-14 | 2007-04-26 | Fujifilm Corp | Composition for organic electroluminescence element, method of manufacturing organic electroluminescence element, and organic electroluminescence element |
JP2007080677A (en) | 2005-09-14 | 2007-03-29 | Fujifilm Corp | Organic electroluminescent element and its manufacturing method |
JP2007110102A (en) | 2005-09-15 | 2007-04-26 | Fujifilm Corp | Organic electroluminescence element |
US7839078B2 (en) | 2005-09-15 | 2010-11-23 | Fujifilm Corporation | Organic electroluminescent element having a luminescent layer and a buffer layer adjacent thereto |
JP2007088105A (en) | 2005-09-20 | 2007-04-05 | Fujifilm Corp | Organic electroluminescence element |
JP4789556B2 (en) | 2005-09-21 | 2011-10-12 | 富士フイルム株式会社 | Organic electroluminescence device |
TWI268952B (en) | 2005-09-21 | 2006-12-21 | Au Optronics Corp | Spiro silane compound and organic electroluminescent device using the same |
JP2007186490A (en) | 2005-12-14 | 2007-07-26 | Sumitomo Seika Chem Co Ltd | Compound for electroluminescent element and method for producing the same |
WO2007097149A1 (en) | 2006-02-20 | 2007-08-30 | Konica Minolta Holdings, Inc. | Organic electroluminescence element, white light emitting element, display device and illuminating device |
US7854513B2 (en) | 2006-03-03 | 2010-12-21 | Quach Cang V | One-way transparent display systems |
JP4945156B2 (en) | 2006-03-24 | 2012-06-06 | 富士フイルム株式会社 | Organic electroluminescence device |
JP5144034B2 (en) | 2006-05-31 | 2013-02-13 | 富士フイルム株式会社 | Organic electroluminescence device |
JP2008010353A (en) | 2006-06-30 | 2008-01-17 | Seiko Epson Corp | Manufacturing method of mask, manufacturing method of wiring pattern, and manufacturing method of plasma display |
DE102006035018B4 (en) | 2006-07-28 | 2009-07-23 | Novaled Ag | Oxazole triplet emitter for OLED applications |
JP2008037848A (en) | 2006-08-10 | 2008-02-21 | Takasago Internatl Corp | Platinum complex and light-emitting element |
JP5205584B2 (en) | 2006-09-06 | 2013-06-05 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device and display device |
US7598381B2 (en) | 2006-09-11 | 2009-10-06 | The Trustees Of Princeton University | Near-infrared emitting organic compounds and organic devices using the same |
JP5049711B2 (en) | 2006-09-27 | 2012-10-17 | 富士フイルム株式会社 | Organic electroluminescence device |
JP2008109085A (en) | 2006-09-29 | 2008-05-08 | Fujifilm Corp | Organic electroluminescent element |
JP2008103535A (en) | 2006-10-19 | 2008-05-01 | Takasago Internatl Corp | Light emitting element |
JP2008108617A (en) | 2006-10-26 | 2008-05-08 | Fujifilm Corp | Organic electroluminescent element |
JP2008117545A (en) | 2006-11-01 | 2008-05-22 | Nix Inc | Joint device for liquid feeding and receiving and fuel cell system equipped with this |
JP4924878B2 (en) | 2006-11-06 | 2012-04-25 | 株式会社ニコン | Absolute encoder |
JP4478166B2 (en) | 2006-11-09 | 2010-06-09 | 三星モバイルディスプレイ株式會社 | Organic light-emitting device provided with organic film containing organometallic complex |
JP2009076834A (en) | 2006-11-27 | 2009-04-09 | Fujifilm Corp | Organic electroluminescednt device, and new indole derivative |
JP5282260B2 (en) | 2006-11-27 | 2013-09-04 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
JP5187493B2 (en) | 2006-11-27 | 2013-04-24 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescent devices and novel indole derivatives |
WO2008066933A2 (en) | 2006-12-01 | 2008-06-05 | The Regents Of The University Of California | Enhancing performance characteristics of organic semiconducting films by improved solution processing |
US8129494B2 (en) | 2006-12-26 | 2012-03-06 | Asahi Kasei E-Materials Corporation | Resin composition for printing plate |
US8106199B2 (en) | 2007-02-13 | 2012-01-31 | Arizona Board Of Regents For And On Behalf Of Arizona State University | Organometallic materials for optical emission, optical absorption, and devices including organometallic materials |
JP4833106B2 (en) | 2007-02-13 | 2011-12-07 | 富士フイルム株式会社 | Organic light emitting device |
DE602008004738D1 (en) | 2007-02-23 | 2011-03-10 | Basf Se | ELECTROLUMINESCENT METAL COMPLEXES WITH BENZOTRIAZOLENE |
JP5230218B2 (en) | 2007-03-26 | 2013-07-10 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
US20080241518A1 (en) | 2007-03-26 | 2008-10-02 | Tasuku Satou | Organic electroluminescence element |
JP5081010B2 (en) * | 2007-03-26 | 2012-11-21 | 富士フイルム株式会社 | Organic electroluminescence device |
ATE512206T1 (en) | 2007-03-28 | 2011-06-15 | Fujifilm Corp | ORGANIC ELECTROLUMINESCENCE DEVICE |
JP5430073B2 (en) | 2007-03-30 | 2014-02-26 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
EP1988079A1 (en) | 2007-04-25 | 2008-11-05 | Lonza Ag | Process for the preparation of optically active ethenylphenyl-alcohols |
JP5084361B2 (en) | 2007-06-18 | 2012-11-28 | 株式会社リコー | Image forming apparatus |
JP2009016579A (en) | 2007-07-04 | 2009-01-22 | Fujifilm Corp | Organic electroluminescent element and manufacturing method |
JP2009016184A (en) | 2007-07-04 | 2009-01-22 | Fujifilm Corp | Organic electroluminescent element |
GB2451106A (en) | 2007-07-18 | 2009-01-21 | Cis Bio Int | Lanthanide (III) ion complexing pyrazoyl-aza(thio)xanthone comprising compounds, their complexes and their use as fluorescent labels |
JP5497259B2 (en) | 2007-07-27 | 2014-05-21 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
JP2009032989A (en) | 2007-07-27 | 2009-02-12 | Fujifilm Corp | Organic electroluminescent element |
JP5255794B2 (en) | 2007-07-27 | 2013-08-07 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
JP2009055010A (en) | 2007-07-27 | 2009-03-12 | Fujifilm Corp | Organic electroluminescent device |
JP5119812B2 (en) | 2007-09-03 | 2013-01-16 | コニカミノルタホールディングス株式会社 | Organic electroluminescence element, display device and lighting device |
KR101548382B1 (en) | 2007-09-14 | 2015-08-28 | 유디씨 아일랜드 리미티드 | Organic electroluminescence device |
JP5014036B2 (en) | 2007-09-18 | 2012-08-29 | 富士フイルム株式会社 | Organic electroluminescence device |
GB0718577D0 (en) | 2007-09-24 | 2007-10-31 | Acal Energy Ltd | Fuel cells |
JP5438941B2 (en) | 2007-09-25 | 2014-03-12 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
US7862908B2 (en) | 2007-11-26 | 2011-01-04 | National Tsing Hua University | Conjugated compounds containing hydroindoloacridine structural elements, and their use |
KR100905951B1 (en) | 2007-12-06 | 2009-07-06 | 주식회사 잉크테크 | Iridium Complex Containing Carbazole-Substituted Pyridine and Phenyl Derivatives as Main Ligand and Organic Light-Emitting Diodes Containing The Same |
JP5438955B2 (en) | 2007-12-14 | 2014-03-12 | ユー・ディー・シー アイルランド リミテッド | Platinum complex compound and organic electroluminescence device using the same |
WO2009086209A2 (en) | 2007-12-21 | 2009-07-09 | Arizona Board Of Regents For And On Behalf Of Arizona State University | Platinum(ii) di(2-pyrazolyl)benzene chloride analogs and uses |
US9293720B2 (en) | 2008-02-19 | 2016-03-22 | New Jersey Institute Of Technology | Carbon nanotubes as charge carriers in organic and hybrid solar cells |
JP5243972B2 (en) | 2008-02-28 | 2013-07-24 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
WO2009111299A2 (en) | 2008-02-29 | 2009-09-11 | Arizona Board Of Regents For And On Behalf Of Arizona State University | Tridentate platinum (ii) complexes |
JP2009211892A (en) | 2008-03-03 | 2009-09-17 | Fujifilm Corp | Organic electroluminescent element |
DE102008015526B4 (en) | 2008-03-25 | 2021-11-11 | Merck Patent Gmbh | Metal complexes |
JP4531836B2 (en) | 2008-04-22 | 2010-08-25 | 富士フイルム株式会社 | Organic electroluminescent device, novel platinum complex compound and novel compound that can be a ligand |
JP2009266943A (en) | 2008-04-23 | 2009-11-12 | Fujifilm Corp | Organic field light-emitting element |
JP4531842B2 (en) | 2008-04-24 | 2010-08-25 | 富士フイルム株式会社 | Organic electroluminescence device |
JP2009267171A (en) | 2008-04-25 | 2009-11-12 | Fujifilm Corp | Organic electric field light emitting element |
JP2009267244A (en) | 2008-04-28 | 2009-11-12 | Fujifilm Corp | Organic electroluminescent element |
JP2009272339A (en) | 2008-04-30 | 2009-11-19 | Fujifilm Corp | Organic electric field light-emitting element |
KR20110031387A (en) | 2008-07-16 | 2011-03-25 | 솔베이(소시에떼아노님) | Light-emitting material comprising multinuclear complexes |
KR20110058808A (en) | 2008-08-20 | 2011-06-01 | 플렉스트로닉스, 인크 | Improved solvent system for fabrication of organic solar cells |
CA2734864A1 (en) | 2008-08-21 | 2010-02-25 | Innova Dynamics, Inc. | Enhanced surfaces, coatings, and related methods |
US7635792B1 (en) | 2008-10-14 | 2009-12-22 | General Electric Company | 2,5-linked polyfluorenes for optoelectronic devices |
WO2010056669A1 (en) | 2008-11-11 | 2010-05-20 | Universal Display Corporation | Phosphorescent emitters |
JP5507185B2 (en) | 2008-11-13 | 2014-05-28 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
WO2010059240A1 (en) | 2008-11-21 | 2010-05-27 | Plextronics, Inc. | Doped interfacial modification layers for stability enhancement for bulk heterojunction organic solar cells |
JP5497284B2 (en) | 2008-12-08 | 2014-05-21 | ユー・ディー・シー アイルランド リミテッド | White organic electroluminescence device |
US8420234B2 (en) * | 2009-01-06 | 2013-04-16 | Udc Ireland Limited | Organic electroluminescent device |
JP5627883B2 (en) | 2009-01-07 | 2014-11-19 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
JP5210187B2 (en) | 2009-01-22 | 2013-06-12 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
KR101066743B1 (en) | 2009-02-13 | 2011-09-21 | 부산대학교 산학협력단 | Iridium complex and organic light-emitting diodes |
US20120108806A1 (en) | 2009-03-12 | 2012-05-03 | Jian Li | Azaporphyrins and applications thereof |
JP5644143B2 (en) | 2009-03-25 | 2014-12-24 | 住友化学株式会社 | Coating method and manufacturing method of organic electroluminescence element |
KR101792266B1 (en) | 2009-04-06 | 2017-10-31 | 아리조나 보드 오브 리전트스, 아리조나주의 아리조나 주립대 대행법인 | Synthesis of four coordinated platinum complexes and their applications in light emitting devices thereof |
CN102396250A (en) | 2009-04-17 | 2012-03-28 | 松下电器产业株式会社 | Apparatus for management of local ip access in segmented mobile communication system |
CN102482402A (en) | 2009-05-21 | 2012-05-30 | 破立纪元有限公司 | Conjugated polymers and their use in optoelectronic devices |
JP2010185068A (en) | 2009-08-31 | 2010-08-26 | Fujifilm Corp | Organic electroluminescent device |
JP5770441B2 (en) | 2009-09-30 | 2015-08-26 | ユー・ディー・シー アイルランド リミテッド | Material for organic electroluminescence device and organic electroluminescence device |
DE102009048791A1 (en) | 2009-10-08 | 2011-04-14 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
WO2011045337A1 (en) | 2009-10-14 | 2011-04-21 | Basf Se | Dinuclear platinum-carbene complexes and the use thereof in oleds |
CN102576805A (en) | 2009-10-30 | 2012-07-11 | 住友化学株式会社 | Organic photoelectric conversion element and process for production thereof |
EP2497130B1 (en) | 2009-11-06 | 2018-01-24 | Nano-C, Inc. | Fullerene-functionalized particles, methods for making the same and their use in bulkheterojunction organic photovoltaic devices |
US20120326103A1 (en) | 2009-11-27 | 2012-12-27 | Shuk Kwan Mak | Functionalized triplet emitters for electro-luminescent devices |
JP5495746B2 (en) | 2009-12-08 | 2014-05-21 | キヤノン株式会社 | Novel iridium complex and organic light emitting device having the same |
EP2517274B1 (en) | 2009-12-23 | 2017-05-24 | Merck Patent GmbH | Compositions comprising polymeric binders |
WO2011118016A1 (en) | 2010-03-26 | 2011-09-29 | トヨタ自動車株式会社 | Hood structure for vehicle |
DE112011101526T5 (en) | 2010-04-30 | 2013-05-16 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Synthesis of four-coordinate palladium complexes and their applications in light-emitting devices |
DE112011101527T5 (en) | 2010-04-30 | 2013-05-16 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Synthesis of four-coordinate gold complexes and their applications in light-emitting devices |
JP5973692B2 (en) | 2010-09-30 | 2016-08-23 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
JP5627979B2 (en) | 2010-09-30 | 2014-11-19 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescence device |
WO2012074909A1 (en) | 2010-11-29 | 2012-06-07 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Methods for fabricating bulk heterojunctions using solution processing techniques |
US8816080B2 (en) | 2011-02-18 | 2014-08-26 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Four coordinated platinum and palladium complexes with geometrically distorted charge transfer state and their applications in light emitting devices |
WO2012116231A2 (en) | 2011-02-23 | 2012-08-30 | Universal Display Corporation | Novel tetradentate platinum complexes |
JP6014350B2 (en) | 2011-04-12 | 2016-10-25 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescent device, organic electroluminescent device material, film, light emitting layer, and organic electroluminescent device manufacturing method |
JP5794813B2 (en) | 2011-04-12 | 2015-10-14 | ユー・ディー・シー アイルランド リミテッド | Organic electroluminescent element, organic electroluminescent element material, film, and method for producing organic electroluminescent element |
WO2012142387A1 (en) * | 2011-04-14 | 2012-10-18 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Pyridine-oxyphenyl coordinated iridium (iii) complexes and methods of making and using |
US10103340B2 (en) | 2011-06-03 | 2018-10-16 | Merck Patent Gmbh | Metal complexes |
US9783564B2 (en) | 2011-07-25 | 2017-10-10 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR101950039B1 (en) | 2011-07-25 | 2019-02-19 | 유니버셜 디스플레이 코포레이션 | Tetradentate platinum complexes |
US9493698B2 (en) | 2011-08-31 | 2016-11-15 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9461254B2 (en) | 2012-01-03 | 2016-10-04 | Universal Display Corporation | Organic electroluminescent materials and devices |
US8987451B2 (en) | 2012-01-03 | 2015-03-24 | Universal Display Corporation | Synthesis of cyclometallated platinum(II) complexes |
US9318725B2 (en) | 2012-02-27 | 2016-04-19 | Jian Li | Microcavity OLED device with narrow band phosphorescent emitters |
CN202549937U (en) | 2012-05-10 | 2012-11-21 | 京东方科技集团股份有限公司 | Organic light-emitting diode (OLED) display structure and OLED display device |
KR101338250B1 (en) | 2012-06-07 | 2013-12-09 | 삼성디스플레이 주식회사 | Display device |
US9502672B2 (en) | 2012-06-21 | 2016-11-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9231218B2 (en) | 2012-07-10 | 2016-01-05 | Universal Display Corporation | Phosphorescent emitters containing dibenzo[1,4]azaborinine structure |
US9059412B2 (en) | 2012-07-19 | 2015-06-16 | Universal Display Corporation | Transition metal complexes containing substituted imidazole carbene as ligands and their application in OLEDs |
GB201213392D0 (en) | 2012-07-27 | 2012-09-12 | Imp Innovations Ltd | Electroluminescent compositions |
US9312502B2 (en) | 2012-08-10 | 2016-04-12 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Iridium complexes demonstrating broadband emission through controlled geometric distortion and applications thereof |
WO2014031977A1 (en) | 2012-08-24 | 2014-02-27 | Arizona Board Of Regents For And On Behalf Of Arizona State University | Metal compounds and methods and uses thereof |
WO2014047616A1 (en) | 2012-09-24 | 2014-03-27 | Arizona Board Of Regents For And On Behalf Of Arizona State University | Metal compounds, methods, and uses thereof |
US9312505B2 (en) | 2012-09-25 | 2016-04-12 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR102145982B1 (en) | 2012-10-24 | 2020-08-19 | 엘지디스플레이 주식회사 | Method for mnufacturing of blue phosphorescence composition and organic light emittin diode comprising the same |
US20150274762A1 (en) | 2012-10-26 | 2015-10-01 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Metal complexes, methods, and uses thereof |
KR102017743B1 (en) | 2013-01-04 | 2019-09-04 | 삼성디스플레이 주식회사 | Organic light-emitting device having improved efficiency characterisitics and organic light-emitting display apparatus including the same |
WO2015027060A1 (en) | 2013-08-21 | 2015-02-26 | Arizona Board Of Regents On Behalf Of Arizona State University | Phosphorescent tetradentate metal complexes having modified emission spectra |
US9673409B2 (en) | 2013-06-10 | 2017-06-06 | Arizona Board Of Regents On Behalf Of Arizona State University | Phosphorescent tetradentate metal complexes having modified emission spectra |
JPWO2014208271A1 (en) | 2013-06-28 | 2017-02-23 | コニカミノルタ株式会社 | ORGANIC ELECTROLUMINESCENT ELEMENT, ITS MANUFACTURING METHOD, AND ORGANIC ELECTROLUMINESCENT DEVICE |
US9735378B2 (en) | 2013-09-09 | 2017-08-15 | Universal Display Corporation | Organic electroluminescent materials and devices |
JP6804823B2 (en) | 2013-10-14 | 2020-12-23 | アリゾナ・ボード・オブ・リージェンツ・オン・ビハーフ・オブ・アリゾナ・ステイト・ユニバーシティーArizona Board of Regents on behalf of Arizona State University | Platinum complex and device |
US9224963B2 (en) | 2013-12-09 | 2015-12-29 | Arizona Board Of Regents On Behalf Of Arizona State University | Stable emitters |
US10020455B2 (en) | 2014-01-07 | 2018-07-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complex emitters containing phenyl-pyrazole and its analogues |
US10056567B2 (en) | 2014-02-28 | 2018-08-21 | Arizona Board Of Regents On Behalf Of Arizona State University | Chiral metal complexes as emitters for organic polarized electroluminescent devices |
EP3741768B1 (en) | 2014-05-08 | 2022-12-07 | Universal Display Corporation | Stabilized imidazophenanthridine materials |
US9941479B2 (en) | 2014-06-02 | 2018-04-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate cyclometalated platinum complexes containing 9,10-dihydroacridine and its analogues |
US9911931B2 (en) | 2014-06-26 | 2018-03-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9923155B2 (en) | 2014-07-24 | 2018-03-20 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) complexes cyclometalated with functionalized phenyl carbene ligands and their analogues |
US9502671B2 (en) | 2014-07-28 | 2016-11-22 | Arizona Board Of Regents On Behalf Of Arizona State University | Tridentate cyclometalated metal complexes with six-membered coordination rings |
US9818959B2 (en) | 2014-07-29 | 2017-11-14 | Arizona Board of Regents on behlaf of Arizona State University | Metal-assisted delayed fluorescent emitters containing tridentate ligands |
US10793546B2 (en) | 2014-08-15 | 2020-10-06 | Arizona Board Of Regents On Behalf Of Arizona State University | Non-platinum metal complexes for excimer based single dopant white organic light emitting diodes |
WO2016029137A1 (en) | 2014-08-22 | 2016-02-25 | Arizona Board Of Regents On Behalf Of Arizona State University | Organic light-emitting diodes with fluorescent and phosphorescent emitters |
US9920242B2 (en) | 2014-08-22 | 2018-03-20 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent materials as co-host materials for fluorescent OLEDs |
US10033003B2 (en) | 2014-11-10 | 2018-07-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes with carbon group bridging ligands |
US9865825B2 (en) | 2014-11-10 | 2018-01-09 | Arizona Board Of Regents On Behalf Of Arizona State University | Emitters based on octahedral metal complexes |
CN104377231B (en) | 2014-12-03 | 2019-12-31 | 京东方科技集团股份有限公司 | Double-sided OLED display panel and display device |
WO2016088354A1 (en) * | 2014-12-05 | 2016-06-09 | 出光興産株式会社 | Metal complex compound, material for organic electroluminescent element, composition, organic electroluminescent element, and electronic device |
US9711739B2 (en) | 2015-06-02 | 2017-07-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes containing indoloacridine and its analogues |
US9879039B2 (en) | 2015-06-03 | 2018-01-30 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate and octahedral metal complexes containing naphthyridinocarbazole and its analogues |
WO2016197019A1 (en) | 2015-06-04 | 2016-12-08 | Jian Li | Transparent electroluminescent devices with controlled one-side emissive displays |
US10158091B2 (en) | 2015-08-04 | 2018-12-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes, devices, and uses thereof |
US10211411B2 (en) | 2015-08-25 | 2019-02-19 | Arizona Board Of Regents On Behalf Of Arizona State University | Thermally activated delayed fluorescent material based on 9,10-dihydro-9,9-dimethylacridine analogues for prolonging device longevity |
US11335865B2 (en) | 2016-04-15 | 2022-05-17 | Arizona Board Of Regents On Behalf Of Arizona State University | OLED with multi-emissive material layer |
US10177323B2 (en) | 2016-08-22 | 2019-01-08 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes and octahedral iridium complexes employing azepine functional groups and their analogues |
WO2018071697A1 (en) | 2016-10-12 | 2018-04-19 | Jian Li | Narrow band red phosphorescent tetradentate platinum (ii) complexes |
US11548905B2 (en) * | 2016-12-15 | 2023-01-10 | Universal Display Corporation | Organic electroluminescent materials and devices |
US11183670B2 (en) | 2016-12-16 | 2021-11-23 | Arizona Board Of Regents On Behalf Of Arizona State University | Organic light emitting diode with split emissive layer |
US11708385B2 (en) | 2017-01-27 | 2023-07-25 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emitters employing pyrido-pyrrolo-acridine and analogues |
US10392387B2 (en) | 2017-05-19 | 2019-08-27 | Arizona Board Of Regents On Behalf Of Arizona State University | Substituted benzo[4,5]imidazo[1,2-a]phenanthro[9,10-c][1,8]naphthyridines, benzo[4,5]imidazo[1,2-a]phenanthro[9,10-c][1,5]naphthyridines and dibenzo[f,h]benzo[4,5]imidazo[2,1-a]pyrazino[2,3-c]isoquinolines as thermally assisted delayed fluorescent materials |
US10516117B2 (en) | 2017-05-19 | 2019-12-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emttters employing benzo-imidazo-phenanthridine and analogues |
US11101435B2 (en) | 2017-05-19 | 2021-08-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complexes based on biscarbazole and analogues |
US10615349B2 (en) | 2017-05-19 | 2020-04-07 | Arizona Board Of Regents On Behalf Of Arizona State University | Donor-acceptor type thermally activated delayed fluorescent materials based on imidazo[1,2-F]phenanthridine and analogues |
US11647643B2 (en) | 2017-10-17 | 2023-05-09 | Arizona Board Of Regents On Behalf Of Arizona State University | Hole-blocking materials for organic light emitting diodes |
WO2019079509A2 (en) | 2017-10-17 | 2019-04-25 | Jian Li | Single-doped white oleds with extraction layer doped with down-conversion red emitters |
CN117279468A (en) | 2017-10-17 | 2023-12-22 | 李健 | Phosphorescent excimer with preferred molecular orientation as monochromatic emitter for display and illumination applications |
US20190276485A1 (en) | 2018-03-09 | 2019-09-12 | Arizona Board Of Regents On Behalf Of Arizona State University | Blue and narrow band green and red emitting metal complexes |
WO2019236541A1 (en) | 2018-06-04 | 2019-12-12 | Jian Li | Color tunable hybrid led-oled illumination devices |
US20210261589A1 (en) | 2018-07-16 | 2021-08-26 | Arizona Board Of Regents On Behalf Of Arizona State University | Fluorinated porphyrin derivatives for optoelectronic applications |
-
2013
- 2013-10-25 US US14/437,963 patent/US20150274762A1/en not_active Abandoned
- 2013-10-25 WO PCT/US2013/066793 patent/WO2014109814A2/en active Application Filing
-
2018
- 2018-02-26 US US15/905,385 patent/US10995108B2/en active Active
-
2021
- 2021-03-25 US US17/212,209 patent/US20210230198A1/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9238668B2 (en) * | 2011-05-26 | 2016-01-19 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University | Synthesis of platinum and palladium complexes as narrow-band phosphorescent emitters for full color displays |
Cited By (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10727422B2 (en) | 2010-04-30 | 2020-07-28 | Arizona Board Of Regents On Behalf Of Arizona State University | Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof |
US10263197B2 (en) | 2010-04-30 | 2019-04-16 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof |
US10414785B2 (en) | 2011-04-14 | 2019-09-17 | Arizona Board Of Regents Acting For And On Behalf Of Arizona State University | Pyridine-oxyphenyl coordinated iridium (III) complexes and methods of making and using |
US10804476B2 (en) | 2011-05-26 | 2020-10-13 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University | Synthesis of platinum and palladium complexes as narrow-band phosphorescent emitters for full color displays |
US11121328B2 (en) | 2011-05-26 | 2021-09-14 | Arizona Board Of Regents On Behalf Of Arizona State University | Synthesis of platinum and palladium complexes as narrow-band phosphorescent emitters for full color displays |
US9711741B2 (en) | 2012-08-24 | 2017-07-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal compounds and methods and uses thereof |
US10622571B2 (en) | 2012-09-24 | 2020-04-14 | Arizona Board Of Regents For And On Behalf Of Arizona State University | Metal compounds, methods, and uses thereof |
US11114626B2 (en) | 2012-09-24 | 2021-09-07 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal compounds, methods, and uses thereof |
US10995108B2 (en) | 2012-10-26 | 2021-05-04 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal complexes, methods, and uses thereof |
US10211414B2 (en) | 2013-06-10 | 2019-02-19 | Arizona Board Of Regents On Behalf Of Arizona State University | Phosphorescent tetradentate metal complexes having modified emission spectra |
US10566553B2 (en) | 2013-10-14 | 2020-02-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Platinum complexes and devices |
US11189808B2 (en) | 2013-10-14 | 2021-11-30 | Arizona Board Of Regents On Behalf Of Arizona State University | Platinum complexes and devices |
US11930698B2 (en) | 2014-01-07 | 2024-03-12 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complex emitters containing phenyl-pyrazole and its analogues |
US10937976B2 (en) | 2014-01-07 | 2021-03-02 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complex emitters containing phenyl-pyrazole and its analogues |
US10020455B2 (en) | 2014-01-07 | 2018-07-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complex emitters containing phenyl-pyrazole and its analogues |
US11839144B2 (en) | 2014-06-02 | 2023-12-05 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate cyclometalated platinum complexes containing 9,10-dihydroacridine and its analogues |
US11011712B2 (en) | 2014-06-02 | 2021-05-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate cyclometalated platinum complexes containing 9,10-dihydroacridine and its analogues |
US10886478B2 (en) | 2014-07-24 | 2021-01-05 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) complexes cyclometalated with functionalized phenyl carbene ligands and their analogues |
US10964897B2 (en) | 2014-07-28 | 2021-03-30 | Arizona Board Of Regents On Behalf Of Arizona State University | Tridentate cyclometalated metal complexes with six-membered coordination rings |
US11145830B2 (en) | 2014-07-29 | 2021-10-12 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emitters containing tridentate ligands |
US10790457B2 (en) | 2014-07-29 | 2020-09-29 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emitters containing tridentate ligands |
US10793546B2 (en) | 2014-08-15 | 2020-10-06 | Arizona Board Of Regents On Behalf Of Arizona State University | Non-platinum metal complexes for excimer based single dopant white organic light emitting diodes |
US11339324B2 (en) | 2014-08-22 | 2022-05-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent materials as co-host materials for fluorescent OLEDs |
US10745615B2 (en) | 2014-08-22 | 2020-08-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent materials as co-host materials for fluorescent OLEDs |
US11795387B2 (en) | 2014-08-22 | 2023-10-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent materials as co-host materials for fluorescent OLEDs |
US11329244B2 (en) | 2014-08-22 | 2022-05-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Organic light-emitting diodes with fluorescent and phosphorescent emitters |
US10294417B2 (en) | 2014-08-22 | 2019-05-21 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent materials as co-host materials for fluorescent OLEDS |
US11563191B2 (en) | 2014-08-29 | 2023-01-24 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element with light-emitting layer including first and second organic compounds, display device, electronic device, and lighting device |
US10714700B2 (en) | 2014-08-29 | 2020-07-14 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, electronic device, and lighting device |
US10693095B2 (en) * | 2014-08-29 | 2020-06-23 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, electronic device, and lighting device |
US20180145273A1 (en) * | 2014-08-29 | 2018-05-24 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, electronic device, and lighting device |
US10944064B2 (en) | 2014-11-10 | 2021-03-09 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes with carbon group bridging ligands |
US10991897B2 (en) | 2014-11-10 | 2021-04-27 | Arizona Board Of Regents On Behalf Of Arizona State University | Emitters based on octahedral metal complexes |
US10033003B2 (en) | 2014-11-10 | 2018-07-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes with carbon group bridging ligands |
US11856840B2 (en) | 2014-11-10 | 2023-12-26 | Arizona Board Of Regents On Behalf Of Arizona State University | Emitters based on octahedral metal complexes |
US11653560B2 (en) | 2014-11-10 | 2023-05-16 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes with carbon group bridging ligands |
US10056564B2 (en) | 2015-06-02 | 2018-08-21 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate metal complexes containing indoloacridine and its analogues |
US10836785B2 (en) | 2015-06-03 | 2020-11-17 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate and octahedral metal complexes containing naphthyridinocarbazole and its analogues |
US11472827B2 (en) | 2015-06-03 | 2022-10-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate and octahedral metal complexes containing naphthyridinocarbazole and its analogues |
US11930662B2 (en) | 2015-06-04 | 2024-03-12 | Arizona Board Of Regents On Behalf Of Arizona State University | Transparent electroluminescent devices with controlled one-side emissive displays |
US10158091B2 (en) | 2015-08-04 | 2018-12-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes, devices, and uses thereof |
US10930865B2 (en) | 2015-08-04 | 2021-02-23 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes, devices, and uses thereof |
US11245078B2 (en) | 2015-08-25 | 2022-02-08 | Arizona Board Of Regents On Behalf Of Arizona State University | Thermally activated delayed fluorescent material based on 9,10-dihydro-9,9-dimethylacridine analogues for prolonging device longevity |
JP2017152585A (en) * | 2016-02-25 | 2017-08-31 | 株式会社ジャパンディスプレイ | Material for organic electroluminescence display device, and organic electroluminescence display device |
US11335865B2 (en) | 2016-04-15 | 2022-05-17 | Arizona Board Of Regents On Behalf Of Arizona State University | OLED with multi-emissive material layer |
US10566554B2 (en) | 2016-08-22 | 2020-02-18 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes and octahedral iridium complexes employing azepine functional groups and their analogues |
US10177323B2 (en) | 2016-08-22 | 2019-01-08 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum (II) and palladium (II) complexes and octahedral iridium complexes employing azepine functional groups and their analogues |
US10822363B2 (en) | 2016-10-12 | 2020-11-03 | Arizona Board Of Regents On Behalf Of Arizona State University | Narrow band red phosphorescent tetradentate platinum (II) complexes |
US11183670B2 (en) | 2016-12-16 | 2021-11-23 | Arizona Board Of Regents On Behalf Of Arizona State University | Organic light emitting diode with split emissive layer |
CN106803543A (en) * | 2017-01-20 | 2017-06-06 | 瑞声科技(南京)有限公司 | Organic light emitting display |
US11708385B2 (en) | 2017-01-27 | 2023-07-25 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emitters employing pyrido-pyrrolo-acridine and analogues |
US10297778B2 (en) | 2017-03-06 | 2019-05-21 | Samsung Electronics Co., Ltd. | Light-emitting device |
CN106972109A (en) * | 2017-04-21 | 2017-07-21 | 瑞声科技(南京)有限公司 | A kind of luminescent device |
US10950807B2 (en) | 2017-04-21 | 2021-03-16 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the organometallic compound, and diagnostic composition including the organometallic compound |
US10988495B2 (en) | 2017-04-25 | 2021-04-27 | Samsung Electronics Co., Ltd. | Organometallic compound, organic-light emitting device including the same, and diagnostic composition including the organometallic compound |
US11063228B2 (en) | 2017-05-19 | 2021-07-13 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emitters employing benzo-imidazo-phenanthridine and analogues |
US11101435B2 (en) | 2017-05-19 | 2021-08-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Tetradentate platinum and palladium complexes based on biscarbazole and analogues |
US10851106B2 (en) | 2017-05-19 | 2020-12-01 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University | Substituted benzo[4,5]imidazo[1,2-F]phenanthridines, dibenzo[I.K]benzo[4,5]imidazo[1,2-F]benzofurophenanthridines and dibenzo[I.K]benzo[4,5]imidazo[1,2-F]benzo[4,5]thienophenanthridines as thermally assisted delayed fluorescent materials |
US11603370B2 (en) | 2017-05-19 | 2023-03-14 | Arizona Board Of Regents On Behalf Of Arizona State University | Substituted heteroaryls as thermally assisted delayed fluorescent materials |
US10516117B2 (en) | 2017-05-19 | 2019-12-24 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal-assisted delayed fluorescent emttters employing benzo-imidazo-phenanthridine and analogues |
US11450816B2 (en) | 2017-05-19 | 2022-09-20 | Arizona Board Of Regents On Behalf Of Arizona State University | Donor-acceptor type thermally activated delayed fluorescent materials based on imidazo[1,2-f]phenanthridine and analogues |
US11889750B2 (en) | 2017-05-23 | 2024-01-30 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the organometallic compound, and diagnostic composition including the organometallic compound |
US10892427B2 (en) | 2017-05-23 | 2021-01-12 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the organometallic compound, and diagnostic composition including the organometallic compound |
US11925104B2 (en) | 2017-07-21 | 2024-03-05 | Samsung Display Co., Ltd. | Organometallic compound and organic light-emitting device including the same |
US11647643B2 (en) | 2017-10-17 | 2023-05-09 | Arizona Board Of Regents On Behalf Of Arizona State University | Hole-blocking materials for organic light emitting diodes |
US11594688B2 (en) | 2017-10-17 | 2023-02-28 | Arizona Board Of Regents On Behalf Of Arizona State University | Display and lighting devices comprising phosphorescent excimers with preferred molecular orientation as monochromatic emitters |
KR102637104B1 (en) | 2017-11-08 | 2024-02-15 | 삼성전자주식회사 | Organometallic compound, organic light emitting device including the same and a composition for diagnosing including the same |
KR20190052552A (en) * | 2017-11-08 | 2019-05-16 | 삼성전자주식회사 | Organometallic compound, organic light emitting device including the same and a composition for diagnosing including the same |
US11878988B2 (en) | 2019-01-24 | 2024-01-23 | Arizona Board Of Regents On Behalf Of Arizona State University | Blue phosphorescent emitters employing functionalized imidazophenthridine and analogues |
US11594691B2 (en) | 2019-01-25 | 2023-02-28 | Arizona Board Of Regents On Behalf Of Arizona State University | Light outcoupling efficiency of phosphorescent OLEDs by mixing horizontally aligned fluorescent emitters |
US11839143B2 (en) | 2019-07-02 | 2023-12-05 | Samsung Display Co., Ltd. | Organometallic compound and organic light-emitting device including same |
US11889749B2 (en) * | 2019-08-09 | 2024-01-30 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including organometallic compound, and diagnostic composition including organometallic compound |
US20210043856A1 (en) * | 2019-08-09 | 2021-02-11 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including organometallic compound, and diagnostic composition including organometallic compound |
US11785838B2 (en) | 2019-10-02 | 2023-10-10 | Arizona Board Of Regents On Behalf Of Arizona State University | Green and red organic light-emitting diodes employing excimer emitters |
US11945985B2 (en) | 2020-05-19 | 2024-04-02 | Arizona Board Of Regents On Behalf Of Arizona State University | Metal assisted delayed fluorescent emitters for organic light-emitting diodes |
Also Published As
Publication number | Publication date |
---|---|
WO2014109814A2 (en) | 2014-07-17 |
US20180194790A1 (en) | 2018-07-12 |
US10995108B2 (en) | 2021-05-04 |
WO2014109814A3 (en) | 2014-10-09 |
WO2014109814A9 (en) | 2014-08-14 |
US20210230198A1 (en) | 2021-07-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20210230198A1 (en) | Metal Complexes, Methods, and Uses Thereof | |
US11114626B2 (en) | Metal compounds, methods, and uses thereof | |
US11653560B2 (en) | Tetradentate metal complexes with carbon group bridging ligands | |
US11145830B2 (en) | Metal-assisted delayed fluorescent emitters containing tridentate ligands | |
US10056564B2 (en) | Tetradentate metal complexes containing indoloacridine and its analogues | |
US10297769B2 (en) | Organic electroluminescent materials and devices | |
US9831442B2 (en) | Organic electroluminescent materials and devices | |
US9156843B2 (en) | Organic electroluminescent device comprising an organic layer containing an indolocarbazole compound | |
US8415031B2 (en) | Electron transporting compounds | |
US9966541B2 (en) | Biscarbazole derivative host materials and green emitter for OLED emissive region | |
US8227801B2 (en) | Bicarbzole containing compounds for OLEDs | |
US20130181190A1 (en) | Novel heteroleptic iridium complexe | |
US9985232B2 (en) | Biscarbazole derivative host materials for OLED emissive region | |
US20120256169A1 (en) | Substituted oligoazacarbazoles for light emitting diodes | |
US20230120308A1 (en) | Compound, material for an organic electroluminescence device and an organic electroluminescence device comprising the compound |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LI, JIAN;TURNER, ERIC;SIGNING DATES FROM 20150821 TO 20150828;REEL/FRAME:036633/0578 |
|
AS | Assignment |
Owner name: NATIONAL SCIENCE FOUNDATION, VIRGINIA Free format text: CONFIRMATORY LICENSE;ASSIGNOR:ARIZONA STATE UNIVERSITY, TEMPE;REEL/FRAME:039516/0332 Effective date: 20160721 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |