WO2011063083A1 - 3-coordinate copper (i) - carbene complexes - Google Patents
3-coordinate copper (i) - carbene complexes Download PDFInfo
- Publication number
- WO2011063083A1 WO2011063083A1 PCT/US2010/057169 US2010057169W WO2011063083A1 WO 2011063083 A1 WO2011063083 A1 WO 2011063083A1 US 2010057169 W US2010057169 W US 2010057169W WO 2011063083 A1 WO2011063083 A1 WO 2011063083A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- complex
- group
- alkyl
- aryl
- heteroaryl
- Prior art date
Links
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 title claims description 17
- 239000003446 ligand Substances 0.000 claims abstract description 124
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims abstract description 39
- 239000010949 copper Substances 0.000 claims abstract description 29
- -1 copper carbene complexes Chemical class 0.000 claims abstract description 18
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052802 copper Inorganic materials 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 121
- 125000003118 aryl group Chemical group 0.000 claims description 117
- 125000001072 heteroaryl group Chemical group 0.000 claims description 107
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 96
- 125000003342 alkenyl group Chemical group 0.000 claims description 95
- 125000000304 alkynyl group Chemical group 0.000 claims description 95
- 125000003545 alkoxy group Chemical group 0.000 claims description 94
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 94
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 93
- 229910052739 hydrogen Inorganic materials 0.000 claims description 89
- 239000001257 hydrogen Substances 0.000 claims description 89
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 89
- 125000001424 substituent group Chemical group 0.000 claims description 50
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 24
- 229910052799 carbon Inorganic materials 0.000 claims description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims description 21
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 20
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 claims description 20
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 claims description 20
- 229910052760 oxygen Inorganic materials 0.000 claims description 20
- 229910052717 sulfur Inorganic materials 0.000 claims description 20
- 125000004429 atom Chemical group 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 19
- 229910052698 phosphorus Inorganic materials 0.000 claims description 16
- 150000003384 small molecules Chemical class 0.000 claims description 16
- 239000012044 organic layer Substances 0.000 claims description 13
- 125000004076 pyridyl group Chemical group 0.000 claims description 13
- 150000004699 copper complex Chemical class 0.000 claims description 12
- 230000004927 fusion Effects 0.000 claims description 12
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 12
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 12
- 230000007935 neutral effect Effects 0.000 claims description 11
- BPMFPOGUJAAYHL-UHFFFAOYSA-N 9H-Pyrido[2,3-b]indole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=N1 BPMFPOGUJAAYHL-UHFFFAOYSA-N 0.000 claims description 10
- WIUZHVZUGQDRHZ-UHFFFAOYSA-N [1]benzothiolo[3,2-b]pyridine Chemical compound C1=CN=C2C3=CC=CC=C3SC2=C1 WIUZHVZUGQDRHZ-UHFFFAOYSA-N 0.000 claims description 9
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 8
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 8
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 8
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 8
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 8
- 150000001721 carbon Chemical group 0.000 claims description 8
- 125000002883 imidazolyl group Chemical group 0.000 claims description 8
- 125000002971 oxazolyl group Chemical group 0.000 claims description 8
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 8
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 8
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 8
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 8
- 125000005247 tetrazinyl group Chemical group N1=NN=NC(=C1)* 0.000 claims description 8
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 8
- 125000004306 triazinyl group Chemical group 0.000 claims description 8
- 125000001425 triazolyl group Chemical group 0.000 claims description 8
- 238000006467 substitution reaction Methods 0.000 claims description 5
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 4
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims description 4
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 4
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 4
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 4
- DPOPAJRDYZGTIR-UHFFFAOYSA-N Tetrazine Chemical compound C1=CN=NN=N1 DPOPAJRDYZGTIR-UHFFFAOYSA-N 0.000 claims description 4
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 4
- 150000003973 alkyl amines Chemical class 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- 229910052785 arsenic Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229910052732 germanium Inorganic materials 0.000 claims description 4
- 229910052745 lead Inorganic materials 0.000 claims description 4
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 150000003536 tetrazoles Chemical class 0.000 claims description 4
- 229910052718 tin Inorganic materials 0.000 claims description 4
- 150000003852 triazoles Chemical class 0.000 claims description 4
- 125000000335 thiazolyl group Chemical group 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 50
- 239000000463 material Substances 0.000 description 49
- 0 CC(C)c1cccc(C(C)C)c1*(C1NC2*(cccc3)c3C3=*c4ccccc4*23)C=C*1c1c(C(C)C)cccc1C(C)C Chemical compound CC(C)c1cccc(C(C)C)c1*(C1NC2*(cccc3)c3C3=*c4ccccc4*23)C=C*1c1c(C(C)C)cccc1C(C)C 0.000 description 26
- 150000001879 copper Chemical class 0.000 description 15
- 239000011541 reaction mixture Substances 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- 125000001309 chloro group Chemical group Cl* 0.000 description 8
- 238000000695 excitation spectrum Methods 0.000 description 8
- 238000004770 highest occupied molecular orbital Methods 0.000 description 8
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 8
- 238000003786 synthesis reaction Methods 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 238000000151 deposition Methods 0.000 description 7
- 239000002019 doping agent Substances 0.000 description 7
- 238000000295 emission spectrum Methods 0.000 description 7
- ATQYNBNTEXNNIK-UHFFFAOYSA-N imidazol-2-ylidene Chemical group [C]1NC=CN1 ATQYNBNTEXNNIK-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- 238000000862 absorption spectrum Methods 0.000 description 6
- 230000005284 excitation Effects 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000011368 organic material Substances 0.000 description 6
- 238000001953 recrystallisation Methods 0.000 description 6
- 230000000903 blocking effect Effects 0.000 description 5
- 238000001672 corrected emission spectrum Methods 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 239000000412 dendrimer Substances 0.000 description 5
- 229920000736 dendritic polymer Polymers 0.000 description 5
- 238000009792 diffusion process Methods 0.000 description 5
- 230000005525 hole transport Effects 0.000 description 5
- 230000005693 optoelectronics Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 230000032258 transport Effects 0.000 description 5
- 239000003086 colorant Substances 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- 238000001869 matrix assisted laser desorption--ionisation mass spectrum Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 238000002390 rotary evaporation Methods 0.000 description 3
- QRUBYZBWAOOHSV-UHFFFAOYSA-M silver trifluoromethanesulfonate Chemical compound [Ag+].[O-]S(=O)(=O)C(F)(F)F QRUBYZBWAOOHSV-UHFFFAOYSA-M 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 239000012312 sodium hydride Substances 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- YNFBMDWHEHETJW-UHFFFAOYSA-N 2-pyridin-2-yl-1h-benzimidazole Chemical compound N1=CC=CC=C1C1=NC2=CC=CC=C2N1 YNFBMDWHEHETJW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005401 electroluminescence Methods 0.000 description 2
- 238000005286 illumination Methods 0.000 description 2
- UEEXRMUCXBPYOV-UHFFFAOYSA-N iridium;2-phenylpyridine Chemical group [Ir].C1=CC=CC=C1C1=CC=CC=N1.C1=CC=CC=C1C1=CC=CC=N1.C1=CC=CC=C1C1=CC=CC=N1 UEEXRMUCXBPYOV-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 238000000059 patterning Methods 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000010129 solution processing Methods 0.000 description 2
- 238000002207 thermal evaporation Methods 0.000 description 2
- NFRYVRNCDXULEX-UHFFFAOYSA-N (2-diphenylphosphanylphenyl)-diphenylphosphane Chemical compound C1=CC=CC=C1P(C=1C(=CC=CC=1)P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 NFRYVRNCDXULEX-UHFFFAOYSA-N 0.000 description 1
- XZDYFCGKKKSOEY-UHFFFAOYSA-N 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dihydro-2h-imidazol-1-ium-2-ide Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N1CCN(C=2C(=CC=CC=2C(C)C)C(C)C)[C]1 XZDYFCGKKKSOEY-UHFFFAOYSA-N 0.000 description 1
- MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-UHFFFAOYSA-N 0.000 description 1
- DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical group C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
- NPRDEIDCAUHOJU-UHFFFAOYSA-N [Pt].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 Chemical compound [Pt].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 NPRDEIDCAUHOJU-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002514 liquid chromatography mass spectrum Methods 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 238000013086 organic photovoltaic Methods 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 238000001394 phosphorus-31 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000005424 photoluminescence Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
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
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
- C07F1/08—Copper 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
-
- 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
- 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
-
- 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
-
- 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
- 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
Definitions
- the claimed invention was made by, on behalf of, and/or in connection with one or more of the following parties to a joint university corporation research agreement: Regents of the University of Michigan, Princeton University, The University of Southern California, and the Universal Display Corporation. The agreement was in effect on and before the date the claimed invention was made, and the claimed invention was made as a result of activities undertaken within the scope of the agreement.
- the present invention relates to phosphorescent copper complexes, and their use in organic light emitting devices (OLEDs). More particularly, the invention relates to phosphorescent complexes comprising a carbene ligand coordinated to a three coordinate copper atom, and devices containing such complexes.
- Opto-electronic devices that make use of organic materials are becoming increasingly desirable for a number of reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials. For example, the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
- OLEDs organic light emitting devices
- the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
- OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting. Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.
- One example of a green emissive molecule is tris(2-phenylpyridine) iridium, denoted Ir(ppy) 3 , which has the structure:
- organic includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices.
- Small molecule refers to any organic material that is not a polymer, and "small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the "small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a
- a dendrimer may be a "small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.
- top means furthest away from the substrate, while “bottom” means closest to the substrate.
- first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is "in contact with” the second layer.
- a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.
- solution processible means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.
- a ligand may be referred to as "photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material.
- a ligand may be referred to as "ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.
- a first "Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or "higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level.
- IP ionization potentials
- a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative).
- a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative).
- the LUMO energy level of a material is higher than the HOMO energy level of the same material.
- a "higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a "lower” HOMO or LUMO energy level.
- a first work function is "greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a "higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.
- Novel phosphorescent complexes are provided, the complexes comprising a carbene ligand coordinated to a three coordinate copper atom.
- the carbene ligand has the formula:
- Formula I. *C is a divalent carbon atom coordinated to a monovalent copper atom Cu.
- Xi and X 2 are substituents independently selected from alkyl, amine, phosphine, heteroalkyl, aryl and heteroaryl. Xi and X 2 may be further substituted, and Xi and X 2 are optionally linked to form a cycle.
- the carbene ligand is
- each of Xi and X 2 independently forms a bond with *C.
- a first bond is formed between *C and an atom ⁇ in substituent Xi
- a second bond is formed between *C and an atom X' 2 in substituent X 2 .
- ⁇ and X' 2 are independently selected from the group consisting of C, N, O, S and P.
- the carbene ligand is monodentate.
- Xi and X 2 are not joined to form a cycle. In another aspect, Xi and X 2 are joined to form a cycle.
- the copper complex is neutral. In another aspect, the copper complex is charged.
- the complex has the formula:
- Yi is independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl. Yi is a monodentate ligand or a bidentate ligand. n is 1 or 2. Preferably, n is 2.
- the complex has the formula: Formula III.
- Yi and Y 2 are substituents that are independently selected from the group consisting of alkyl, heteroalkyl, aryl and heteroaryl. Yi and Y 2 may be further substituted. Yi and Y 2 are joined. Each of Yi and Y 2 form a bond with Cu. A first bond is formed between Cu and an atom ⁇ in substituent Yi and a second bond is formed between Cu and an atom Y' 2 in substituent Y 2 .
- ⁇ is selected from the group consisting of N, P, *C, O, and S.
- Y' 2 is selected from the group consisting of N, P, *C, tetravalent carbon, O, and S.
- ⁇ is N.
- the ring comprising Cu, ⁇ and Y' 2 is a 5- membered or 6-membered ring.
- Y 1 is selected from the group consisting of pyridyl, pyrazole, alkyl amine, imidazole, benzimidazole, triazole, tetrazole, pyridazine, pyrimidine, pyrazine, triazine, tetrazine, oxazole, thiazole, benzoxazole and benzothiazole.
- Yi- Y 2 is selected from the group consisting of:
- ⁇ X is selected from the group consisting of NR, O, S, Se, CR 2 , and CO.
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Each ring is further substituted by a substituent selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- each R includes a substituent independently selected from the group consisting of carbazole, dibenzofuran, dibenzothiophene, azacarbazole,
- Y Y 2 is selected from the group consisting of:
- X is selected from the group consisting of NR, O, S, Se, CR 2 , and CO.
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Each ring is further substituted by a substituent selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- each R includes a substituent independently selected from the group consisting of carbazole, dibenzofuran, dibenzothiophene, azacarbazole, azadibenzofuran, and azadibenzothiophene.
- Y is an unconjugated, monoanionic ligand containing BY 4 ⁇ , SO3Y “ , CY 4 " , Si0 4 " , OY 2 " , or SY 2 " .
- Each Y is independently selected from the group consisting of hydrogen, alkyl, aryl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl and heteroaryl.
- Yi is BY 4 " .
- the ligand Yi comprises two
- the ligand Yi has the formula:
- the ligand Yi that comprises two monodentate ligands, at least one of which is BY 4 " is selected from the group consisting of:
- Yi and Y 2 are independently selected from the group consisting of pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, pyrazolyl, imidazolyl, benzimidazolyl, oxazolyl, thiazolyl, benzoxazolyl, benzothiazolyl and phosphine.
- Yi and Y 2 may be extended by fusion, e.g., benzanulation. Additionally, Yi and Y 2 may be further substituted with alkyl, aryl, donor or acceptor groups.
- Y 3 and Y 4 are independently selected from the group consisting of hydrogen, alkyl, aryl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteralkyl and heteroaryl. In one aspect, Y 3 and Y 4 are joined to form a cycle, may be extended by fusion, e.g., benzanulation.
- Yi is a bidentate ligand having the formula BY 4 " .
- the ligand Yi is selected from the group consisting of: .
- Yi is a bidentate chelating ligand having the formula: .
- Y'i-Y"i represents a neutral, i.e., uncharged, chealting ligand.
- Y'i-Y"i are capable of coordinating to a metal center.
- ⁇ - ⁇ ' ⁇ ligand examples include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Yi and Y 2 are independently selected from the group consisting of pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, pyrazolyl, imidazolyl, benzimidazolyl, oxazolyl, thiazolyl, benzoxazolyl, benzothiazolyl and phosphine.
- Yi and Y 2 may be extended by fusion, e.g., benzanulation. Additionally, Yi and Y 2 may be further substituted with alkyl, aryl, donor or acceptor groups.
- Y ⁇ and Y 4 are independently selected from the group consisting of hydrogen, alkyl, aryl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteralkyl and heteroaryl.
- Y 3 and Y 4 are joined to form a cycle, which may be extended by fusion, e.g., benzanulation.
- Yi and Y 2 are the same.
- Specific examples of ligands where Yi and Y 2 are the same include, but are not limited to, ligands selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- C* is a divalent carbon atom, n is 0, 1 , or 2.
- m is 0, 1, or 2.
- Y 1 and Y 2 are different.
- Specific examples of ligands where Yi and Y 2 are different include, but are not limited to, ligands selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Yi is SO 3 Y " .
- Specific examples of ligands Y; having the formula SO 3 Y " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Yi is CY 4 ⁇ .
- CY 4 has the formula:
- ligands Yi having the formula CY 4 " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Yi is SiY 4 ⁇ .
- ligands Y; having the formula S1Y 4 " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Yi is OY 2 ⁇ .
- OY 2 " has the formula:
- ligands Yi having the formula OY 2 " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Y; is SY 2 ⁇ .
- SY 2 " has the formula:
- ligands Y having the formula S Y 2 ⁇ include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- the complex comprises two copper (I) centers.
- complexes comprising two copper (I) centers include complexes selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- the carbene ligand is selected from the group consisting of:
- each R includes a substituent independently selected from the group consisting of carbazole, dibenzofuran, dibenzothiophene, azacarbazole,
- the carbene is . More preferably, the carbene is
- R' i and R' 2 may represent mono, di, tri, or tetra substitutions.
- R' i and R' 2 are independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- at least one of R' i and R' 2 is an alkyl having three or more carbon atoms.
- the complex is selected from the group consisting of:
- the complex is selected from the group consisting of:
- Complex 3 Complex 4 ore preferably, the complex is:
- the complex has the formula:
- the complex is selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- the carbene ligand is bidentate.
- the complex is selected from the group consisting of: .
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Z is a monodentate ligand.
- the complex is included in a polymer.
- the complex is included in the repeat unit of the polymer.
- the complex is pendant on the polymer.
- the polymer is selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- m is greater than 2.
- n is 0-20.
- the complex is included in a dendritic complex.
- the dendritic complex is
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- m is greater than 1.
- n is 0-20.
- the complex is included in a small molecule.
- a first device comprising an organic light emitting device further comprising an anode, a cathode; and an organic layer, disposed between the anode and the cathode.
- the organic layer further comprising a phosphorescent complex itself comprising a three coordinate copper atom and a carbene ligand.
- the first device is a consumer product.
- the device may comprise a complex having Formula I, Formula II, Formula III, or Formula IV, as described above.
- Selections for the substituents, ligands, and complexes described as preferred for the complexes having Formula I, Formula II, Formula III, or Formula IV are also preferred for use in a device that comprises a complex including a complex having Formula I, Formula II, Formula III, or Formula IV. These selections include those described for X ls X 2 , X'i, X' 2 ,
- FIG. 1 shows an organic light emitting device.
- FIG. 2 shows an inverted organic light emitting device that does not have a separate electron transport layer.
- FIG. 3 shows complexes comprising a carbene ligand coordinated to a three coordinate copper atom.
- FIG. 4 shows 1H-NMR spectrum of Complex 1.
- FIG. 5 shows 1H-NMR spectrum of Complex 2.
- FIG. 6 shows 1H-NMR spectrum of Complex 3.
- FIG. 7 shows 1H-NMR spectrum of Complex 4.
- FIG. 8 shows MALDI spectrum of Complex 1.
- FIG. 9 shows MALDI spectrum of Complex 2.
- FIG. 10 shows MALDI spectrum of Complex 3.
- FIG. 11 shows MALDI spectrum of Complex 4.
- FIG. 12 shows the absorption spectrum of Complex 1.
- FIG. 13 shows the absorption spectrum of Complex 2.
- FIG. 14 shows the absorption spectrum of Complex 3.
- FIG. 15 shows the absorption spectrum of Complex 4.
- FIG. 16A shows absorption spectrum of Complex 4
- FIG. 16B shows the emission spectra of Complex 4.
- FIG. 17A shows excitation and emission spectra of Complex 1
- FIG. 17B shows excitation and emission spectra of Complex 2.
- FIG. 18A shows excitation and emission spectra of Complex 3
- FIG. 18B shows excitation and emission spectra of Complex 4.
- FIG. 19A shows the x-ray structure of Complex 2
- FIG. 19B shows the x-ray structure of Complex 4.
- FIG. 20 shows the 31 P-NMR spectrum of Complex 1.
- FIG 21. shows the ⁇ -NMR spectrum of Complex 5.
- FIG. 22 shows the X-ray structure of Complex 5.
- FIG. 23 shows LCMS spectrum of Complex 6.
- FIG. 24A shows corrected emission and excitation spectra of Complex 5 in
- FIG. 24B shows corrected emission and excitation spectra of Complex 6 in 2MeTHF at 77K.
- FIG. 25 shows a corrected emission spectrum of Complex 4 in PMMA film at room temperature.
- FIG. 26A shows a corrected emission spectrum of Complex 4 in CH 2 CI 2 at room temperature
- FIG. 26B shows a corrected emission spectrum of Complex 2 in CH 2 CI 2 at room temperature.
- FIG. 27 shows 1H-NMR spectrum of Complex 7.
- FIG. 28A shows 1H-NMR spectrum of Complex 7
- FIG. 28B shows the n B-NMR spectrum of Complex 7.
- FIG. 29A shows excitation and emission spectra of Complex 7 in 2MeTHF at 77K
- FIG. 29B shows excitation and emission spectra of Complex 8 in 2MeTHF at 77K.
- FIG. 30A shows absorption spectrum of Complex 7
- FIG. 30B shows the X-ray structure of Complex 7.
- an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode.
- the anode injects holes and the cathode injects electrons into the organic layer(s).
- the injected holes and electrons each migrate toward the oppositely charged electrode.
- an "exciton” which is a localized electron-hole pair having an excited energy state, is formed.
- Light is emitted when the exciton relaxes via a photoemissive mechanism.
- the exciton may be localized on an excimer or an exciplex. Non- radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.
- the initial OLEDs used emissive molecules that emitted light from their singlet states ("fluorescence") as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.
- FIG. 1 shows an organic light emitting device 100.
- Device 100 may include a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, and a cathode 160.
- Cathode 160 is a complex cathode having a first conductive layer 162 and a second conductive layer 164.
- Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in US 7,279,704 at cols. 6- 10, which are incorporated by reference.
- each of these layers are available.
- a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety.
- An example of a p-doped hole transport layer is m- MTDATA doped with F.sub.4-TCNQ at a molar ratio of 50: 1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety.
- Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to
- n- doped electron transport layer is BPhen doped with Li at a molar ratio of 1 : 1 , as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety.
- FIG. 2 shows an inverted OLED 200.
- the device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230.
- Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an "inverted" OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200.
- FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.
- FIGS. 1 and 2 The simple layered structure illustrated in FIGS. 1 and 2 is provided by way of non- limiting example, and it is understood that embodiments of the invention may be used in connection with a wide variety of other structures.
- the specific materials and structures described are exemplary in nature, and other materials and structures may be used.
- Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers.
- hole transport layer 225 transports holes and injects holes into emissive layer 220, and may be described as a hole transport layer or a hole injection layer.
- an OLED may be described as having an "organic layer" disposed between a cathode and an anode. This organic layer may comprise a single layer, or may further comprise multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2.
- OLEDs having a single organic layer may be used.
- OLEDs may be stacked, for example as described in U.S. Pat. No. 5,707,745 to Forrest et al, which is incorporated by reference in its entirety.
- the OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2.
- the substrate may include an angled reflective surface to improve out-coupling, such as a mesa structure as described in U.S. Pat. No.
- any of the layers of the various embodiments may be deposited by any suitable method.
- preferred methods include thermal evaporation, ink-jet, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102 to Forrest et al, which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. patent application Ser. No. 10/233,470, which is incorporated by reference in its entirety.
- OVPD organic vapor phase deposition
- OJP organic vapor jet printing
- Other suitable deposition methods include spin coating and other solution based processes. Solution based processes are preferably carried out in nitrogen or an inert atmosphere.
- preferred methods include thermal evaporation.
- Preferred patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. No
- 6,294,398 and 6,468,819 which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and OVJD. Other methods may also be used.
- the materials to be deposited may be modified to make them compatible with a particular deposition method.
- substituents such as alkyl and aryl groups, branched or unbranched, and preferably containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having 20 carbons or more may be used, and 3-20 carbons is a preferred range.
- Materials with asymmetric structures may have better solution processibility than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize.
- Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.
- Devices fabricated in accordance with embodiments of the invention may be incorporated into a wide variety of consumer products, including flat panel displays, computer monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads up displays, fully transparent displays, flexible displays, laser printers, telephones, cell phones, personal digital assistants (PDAs), laptop computers, digital cameras, camcorders, viewfmders, micro-displays, vehicles, a large area wall, theater or stadium screen, or a sign.
- PDAs personal digital assistants
- Various control mechanisms may be used to control devices fabricated in accordance with the present invention, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18 degrees C. to 30 degrees C, and more preferably at room temperature (20-25 degrees C).
- the materials and structures described herein may have applications in devices other than OLEDs.
- other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures.
- organic devices such as organic transistors, may employ the materials and structures.
- halo halogen, alkyl, cycloalkyl, alkenyl, alkynyl, arylkyl, heterocyclic group, aryl, aromatic group, and heteroaryl are known to the art, and are defined in U.S. 7,279,704 at cols. 31-32, which are incorporated herein by reference.
- the complexes include a monodentate or a bidentate carbene ligand coordinated to a three coordinate copper atom.
- the complex can be either charged or neutral.
- OLEDs organic light emitting diodes
- the chelating anionic ligand is a high triplet energy ligand, capable of supporting metal-to-ligand charge transfer interactions.
- the complexes in this class may provide high energy phosphorescence, which can be useful in the fabrication of doped OLEDs, in which the copper complex is an emissive dopant.
- These materials may also be used as host materials to support an emissive dopant in an OLED structure.
- a dipyridyl borate complex in this class of compounds has an emission maximum of 475 nm and a photoluminescence efficiency of 0.95 in the solid state. Suitable substitution of the pyridyl groups can red or blue shift this emission substantially.
- the ability to tune emission energies may make these copper complexes excellent emitters and host materials for OLEDs. It is thought that the emission energy may be shifted high enough to make these compounds suitable host materials for deep blue to violet emissive dopants.
- Phosphorescent OLEDs have relied largely on heavy metal complexes as emitters. In particular, devices often utilize emitters containing Ir or Pt to induce spin orbit coupling. Tetrahedral copper complexes have been reported, and are known to phosphoresce at room temperature. However, tetrahedral copper complexes may have certain limitations. In particular, flattening distortions may increase the non-radiative rate, which leads to a decrease in luminescence efficiency. Trigonal planar copper carbene complexes have now been found to give efficient phosphorescence at room temperature. We believe that this is the first observation of phosphorescence from trigonal planar copper complexes.
- Trigonal planar copper complexes may also have several advantages for use in OLEDs.
- the trigonal planar copper complexes have comparatively short lifetimes, in the tens of microsecond range (see Table 1).
- Table 1 shows the lifetimes of several different trigonal planar copper carbene complexes.
- the lifetime of the trigonal copper complex is longer than an Ir complex (i.e., 1-10 ⁇ ) but shorter than that of a platinum porphyrin complex.
- Trigonal planar copper complexes may also be particularly useful in OLEDs used for certain applications.
- copper complexes provide a broader line spectrum which is especially useful for lighting applications.
- a device comprising a trigonal planar copper complex in combination with only one other complex may cover red, green, and blue colors.
- a device comprising a trigonal planar copper complex and a blue emitter may cover all colors required for lighting.
- Novel phosphorescent complexes are provided, the complexes comprising a carbene ligand coordinated to a three coordinate copper atom.
- the carbene ligand has the formula:
- *C is a divalent carbon atom coordinated to a monovalent copper atom Cu.
- Xi and X 2 are substituents independently selected from alkyl, amine, phosphine, heteroalkyl, aryl and heteroaryl. Xi and X 2 may be further substituted, and Xi and X 2 are optionally linked to form a cycle.
- the carbene ligand is monodentate.
- each of Xi and X 2 independently forms a bond with *C.
- a first bond is formed between *C and an atom ⁇ in substituent Xi
- a second bond is formed between *C and an atom X' 2 in substituent X 2 .
- ⁇ and X' 2 are independently selected from the group consisting of C, N, O, S and P.
- the carbene ligand is monodentate.
- Xi and X 2 are not joined to form a cycle. In another aspect, Xi and X 2 are joined to form a cycle.
- the copper complex is neutral.
- Neutral complexes may be
- a neutral complex can be deposited via vapor deposition.
- the copper complex is charged.
- the complex has the formula:
- Yi is independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl. Yi is a monodentate ligand or a bidentate ligand. n is 1 or 2. Preferably, n is 2.
- the complex has the formula:
- Yi and Y 2 are substituents that are independently selected from the group consisting of alkyl, heteroalkyl, aryl and heteroaryl. Yi and Y 2 may be further substituted. Yi and Y 2 are joined. Each of Yi and Y 2 form a bond with Cu. A first bond is formed between Cu and an atom ⁇ in substituent Y 1 and a second bond is formed between Cu and an atom Y' 2 in substituent Y 2 .
- Y is selected from the group consisting of N, P, *C, O, and S.
- Y' 2 is selected from the group consisting of N, P, *C, tetravalent carbon,
- ⁇ is N.
- the Cu atom, the ⁇ atom and the Y' 2 atom in the complex are included in a ring that can be, for example, a 4-membered, 5-membered, 6-membered, 7-membered, or 8- membered ring.
- the ring comprising Cu, ⁇ and Y' 2 is a 5-membered or 6- membered ring.
- Y 1 is selected from the group consisting of pyridyl, pyrazole, alkyl amine, imidazole, benzimidazole, triazole, tetrazole, pyridazine, pyrimidine, pyrazine, triazine, tetrazine, oxazole, thiazole, benzoxazole and benzothiazole.
- Yi- Y 2 is selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Each ring is further substituted by a substituent selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- each R includes a substituent independently selected from the group consisting of carbazole, dibenzofuran, dibenzothiophene, azacarbazole, azadibenzofuran, and azadibenzothiophene.
- Yi- Y 2 is selected from the group consisting of:
- X is selected from the group consisting of NR, O, S, Se, CR 2 , and CO.
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Each ring is further substituted by a substituent selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- each R includes a substituent independently selected from the group consisting of carbazole, dibenzofuran, dibenzothiophene, azacarbazole, azadibenzofuran, and azadibenzothiophene.
- Y is an unconjugated, monoanionic ligand containing BY 4 ⁇ , SO3Y “ , CY 4 " , Si0 4 " , OY 2 " , or SY 2 " .
- Each Y is independently selected from the group consisting of hydrogen, alkyl, aryl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteralkyl and heteroaryl.
- Y is BY 4 " .
- the ligand Yi comprises two
- the ligand Y has the formula:
- the ligand Y that comprises two monodentate ligands, at least one of which is BY 4 " , is selected from the group consisting of:
- Yi and Y 2 are independently selected from the group consisting of pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, pyrazolyl, imidazolyl, benzimidazolyl, oxazolyl, thiszolyl, benzoxazolyl, benzothiazolyl and phosphine.
- Yi and Y 2 may be extended by fusion, e.g., benzanulation. Additionally, Yi and Y 2 may be further substituted with alkyl, aryl, donor or acceptor groups.
- Y 3 and Y 4 are independently selected from the group consisting of hydrogen, alkyl, aryl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteralkyl and heteroaryl. In one aspect, Y 3 and Y 4 are joined to form a cycle, may be extended by fusion, e.g., benzanulation.
- Yi is a bidentate ligand having the formula BY 4 " .
- the ligand Y is selected from the group consisting of:
- Yi is a bidentate chelating ligand having the formula: .
- Y'i-Y"i represents a neutral, i.e., uncharged, chelating ligand.
- Y'i-Y"i are capable of coordinating to a metal center.
- ⁇ - ⁇ ' ⁇ ligand examples include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Yi and Y 2 are independently selected from the group consisting of pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, pyrazolyl, imidazolyl, benzimidazolyl, oxazolyl, thiszolyl, benzoxazolyl, benzothiazolyl and phosphine.
- Yi and Y 2 may be extended by fusion, e.g., benzanulation. Additionally, Yi and Y 2 may be further substituted with alkyl, aryl, donor or acceptor groups.
- Y 3 and Y 4 are independently selected from the group consisting of hydrogen, alkyl, aryl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteralkyl and heteroaryl. In one aspect, Y 3 and Y 4 are joined to form a cycle, which may be extended by fusion, e.g., benzanulation.
- Yi and Y 2 are the same.
- Specific examples of ligands where Yi and Y 2 are the same include, but are not limited to, ligands selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- C* is a divalent carbon atom, n is 0, 1, or 2.
- m is 0, 1, or 2.
- Y 1 and Y 2 are different.
- Specific examples of ligands where Yi and Y 2 are different include, but are not limited to, ligands selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Yi is SO 3 Y " .
- Specific examples of ligands Y; having the formula SO 3 Y " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Yi is CY 4 ⁇ .
- CY 4 has the formula:
- ligands Yi having the formula CY 4 " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Yi is SiY 4 ⁇ .
- ligands Y; having the formula S1Y 4 " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Yi is OY 2 ⁇ .
- OY 2 " has the formula:
- ligands Yi having the formula OY 2 " include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Y 3 and Y 4 are selected from the group consisting of:
- Y; is SY 2 ⁇ .
- SY 2 " has the formula:
- ligands Yi having the formula SY 2 ⁇ include, but are not limited to, ligands having the structure:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- the complex comprises two copper (I) centers.
- complexes comprising two copper (I) centers include complexes selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- the carbene ligand is selected from the group consisting of:
- the carbene is . More preferably, the carbene is
- R' i and R' 2 may represent mono, di, tri, or tetra substitutions.
- R' i and R' 2 are independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- at least one of R' i and R' 2 is an alkyl having three or more carbon atoms.
- the complex is selected from the group consisting of:
- the complex is selected from the group consisting of:
- Complex 3 Complex 4 ore preferably, the complex is:
- the complex has the formula:
- the complex is selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- the carbene ligand is bidentate.
- the complex is selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- Z is a monodentate ligand.
- the complex is included in a polymer.
- the complex is included in the repeat unit of the polymer.
- the complex is pendant on the polymer.
- the polymer is selected from the group consisting of:
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- m is greater than 2.
- n is 0-20.
- the complex is included in a dendritic complex.
- the dendritic complex is
- Each R is independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, heteroalkyl, aryl and heteroaryl.
- m is greater than 1.
- n is 0-20.
- the complex is included in a small molecule.
- a first device comprising an organic light emitting device further comprising an anode, a cathode; and an organic layer, disposed between the anode and the cathode.
- the organic layer further comprising a phosphorescent complex itself comprising a three coordinate copper atom and a carbene ligand.
- the first device is a consumer product.
- the device may comprise a complex having Formula I, Formula II, Formula III, or Formula IV, as described above.
- Selections for the substituents, ligands, and complexes described as preferred for the complexes having Formula I, Formula II, Formula III, or Formula IV are also preferred for use in a device that comprises a complex including a complex having Formula I, Formula II, Formula III, or Formula IV. These selections include those described for X ls X 2 , X'i, X' 2 ,
- Such devices may contain the trigonal copper complex as a neat thin film.
- an OLED comprising a pure film of the complex may have a higher luminescent efficiency than an OLED that comprises the complex doped with another material.
- the materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device.
- emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present.
- the materials described or referred to below are non-limiting examples of materials that may be useful in combination with the complexes disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710567865.XA CN107793437B (en) | 2009-11-19 | 2010-11-18 | 3-Coordinated copper (I) -carbene complexes |
JP2012540041A JP2013511532A (en) | 2009-11-19 | 2010-11-18 | 3-coordinate copper (I) -carbene complex |
CN201080059525.2A CN102695711B (en) | 2009-11-19 | 2010-11-18 | 3 coordination copper (I) arbine complexes |
KR1020127015896A KR101822668B1 (en) | 2009-11-19 | 2010-11-18 | 3-coordinate copper(i)-carbene complexes |
IN5146DEN2012 IN2012DN05146A (en) | 2009-11-19 | 2010-11-18 | |
EP10832153.0A EP2501707B1 (en) | 2009-11-19 | 2010-11-18 | 3-coordinate copper (i) - carbene complexes |
Applications Claiming Priority (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26280409P | 2009-11-19 | 2009-11-19 | |
US61/262,804 | 2009-11-19 | ||
US30136210P | 2010-02-04 | 2010-02-04 | |
US61/301,362 | 2010-02-04 | ||
US39880810P | 2010-07-01 | 2010-07-01 | |
US61/398,808 | 2010-07-01 | ||
US40298910P | 2010-09-09 | 2010-09-09 | |
US61/402,989 | 2010-09-09 | ||
US12/948,396 US8580394B2 (en) | 2009-11-19 | 2010-11-17 | 3-coordinate copper(I)-carbene complexes |
US12/948,396 | 2010-11-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011063083A1 true WO2011063083A1 (en) | 2011-05-26 |
Family
ID=44059980
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2010/057169 WO2011063083A1 (en) | 2009-11-19 | 2010-11-18 | 3-coordinate copper (i) - carbene complexes |
Country Status (8)
Country | Link |
---|---|
US (2) | US8580394B2 (en) |
EP (1) | EP2501707B1 (en) |
JP (2) | JP2013511532A (en) |
KR (1) | KR101822668B1 (en) |
CN (2) | CN107793437B (en) |
IN (1) | IN2012DN05146A (en) |
TW (1) | TWI513796B (en) |
WO (1) | WO2011063083A1 (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102011003192A1 (en) * | 2011-01-26 | 2012-07-26 | Siemens Aktiengesellschaft | Dopant for organic hole conductors |
WO2013014066A1 (en) * | 2011-07-26 | 2013-01-31 | Eberhard Karls Universität Tübingen | Complex compounds that comprise a ligand having an n- and a p-donor, and use thereof in the optoelectronic field |
EP2554625A1 (en) * | 2011-08-02 | 2013-02-06 | cynora GmbH | Singlet harvesting with two-core copper(I) complexes for opto-electronic devices |
DE102011084639A1 (en) * | 2011-10-17 | 2013-04-18 | Osram Opto Semiconductors Gmbh | ORGANIC ELECTRONIC COMPONENT WITH DUTY, USE OF A DOPING AGENT AND METHOD FOR PRODUCING THE DUTY |
EP2623508A1 (en) | 2012-02-02 | 2013-08-07 | Konica Minolta Advanced Layers, Inc. | Iridium complex compound, organic electroluminescent element material, organic electroluminescent element, illumination device and display device |
US8786179B2 (en) | 2012-09-17 | 2014-07-22 | Universal Display Corporation | Light emitting device comprising phosphorescent materials for white light generation |
JP2014527292A (en) * | 2011-07-26 | 2014-10-09 | メルク パテント ゲーエムベーハー | Complex compounds comprising anionic ligands with two P-donors and their use in the field of optoelectronics |
US9178159B2 (en) | 2011-07-25 | 2015-11-03 | Merck Patent Gmbh | Copolymers with functionalized side chains |
US9246103B2 (en) | 2011-07-25 | 2016-01-26 | Merck Patent Gmbh | Polymers and oligomers with functionalized side groups |
US9553276B2 (en) | 2011-07-26 | 2017-01-24 | Merck Patent Gmbh | Complex compounds having tetradentate ligands and the use thereof in the opto-electronic field |
WO2017046572A1 (en) * | 2015-09-14 | 2017-03-23 | University Of East Anglia | Metal complexes |
US10128450B2 (en) | 2013-10-23 | 2018-11-13 | University Of Southern California | Organic electroluminescent materials and devices |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8580394B2 (en) * | 2009-11-19 | 2013-11-12 | Universal Display Corporation | 3-coordinate copper(I)-carbene complexes |
KR102556025B1 (en) * | 2014-09-17 | 2023-07-19 | 삼성디스플레이 주식회사 | Organometallic complex and organic light emitting diode comprising the same |
GB2540132A (en) * | 2015-06-30 | 2017-01-11 | Cambridge Display Tech Ltd | Compound, composition and organic light-emitting device |
US11111432B2 (en) * | 2018-01-02 | 2021-09-07 | Beijing Normal University | Triangular carbon quantum dots and compositions and uses thereof |
US11920070B2 (en) | 2019-07-12 | 2024-03-05 | The University Of Southern California | Luminescent janus-type, two-coordinated metal complexes |
CN112500582B (en) * | 2020-12-15 | 2022-03-29 | 北京工业大学 | Multinuclear cobalt cluster metal organic framework material based on four-head pyrazole ligand, preparation and application |
US20230165135A1 (en) * | 2021-11-23 | 2023-05-25 | Versitech Limited | d10 METAL CARBENE COMPLEXES FOR OLED APPLICATIONS |
Citations (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4769292A (en) | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
US5247190A (en) | 1989-04-20 | 1993-09-21 | Cambridge Research And Innovation Limited | Electroluminescent devices |
US5627164A (en) * | 1995-06-13 | 1997-05-06 | Exxon Research And Engineering Company | Pyrazolyl borates complexes-(LAW294) |
US5703436A (en) | 1994-12-13 | 1997-12-30 | The Trustees Of Princeton University | Transparent contacts for organic devices |
US5707745A (en) | 1994-12-13 | 1998-01-13 | The Trustees Of Princeton University | Multicolor organic light emitting devices |
US5834893A (en) | 1996-12-23 | 1998-11-10 | The Trustees Of Princeton University | High efficiency organic light emitting devices with light directing structures |
US5844363A (en) | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
US6013982A (en) | 1996-12-23 | 2000-01-11 | The Trustees Of Princeton University | Multicolor display devices |
US6087196A (en) | 1998-01-30 | 2000-07-11 | The Trustees Of Princeton University | Fabrication of organic semiconductor devices using ink jet printing |
US6091195A (en) | 1997-02-03 | 2000-07-18 | The Trustees Of Princeton University | Displays having mesa pixel configuration |
US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
US6294398B1 (en) | 1999-11-23 | 2001-09-25 | The Trustees Of Princeton University | Method for patterning devices |
US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
US6337102B1 (en) | 1997-11-17 | 2002-01-08 | The Trustees Of Princeton University | Low pressure vapor phase deposition of organic thin films |
US20030230980A1 (en) | 2002-06-18 | 2003-12-18 | Forrest Stephen R | Very low voltage, high efficiency phosphorescent oled in a p-i-n structure |
US20040174116A1 (en) | 2001-08-20 | 2004-09-09 | Lu Min-Hao Michael | Transparent electrodes |
US20040192664A1 (en) * | 2003-01-07 | 2004-09-30 | Klaus Kunz | Copper-carbene complexes and their use |
WO2005019373A2 (en) | 2003-08-19 | 2005-03-03 | Basf Aktiengesellschaft | Transition metal complexes comprising carbene ligands serving as emitters for organic light-emitting diodes (oled's) |
US20050258742A1 (en) * | 2004-05-18 | 2005-11-24 | Yui-Yi Tsai | Carbene containing metal complexes as OLEDs |
US20050260446A1 (en) * | 2004-05-18 | 2005-11-24 | Mackenzie Peter B | Cationic metal-carbene complexes |
US20060024522A1 (en) * | 2004-05-18 | 2006-02-02 | Thompson Mark E | Luminescent compounds with carbene ligands |
US7279704B2 (en) | 2004-05-18 | 2007-10-09 | The University Of Southern California | Complexes with tridentate ligands |
JP2007297347A (en) | 2006-05-02 | 2007-11-15 | Ube Ind Ltd | Substituted phenylethynylcopper-nitrogen-containing heterocyclic carbene complex and organic electroluminescent device using the same |
JP2008303152A (en) | 2007-06-05 | 2008-12-18 | Idemitsu Kosan Co Ltd | New copper complex and organic electroluminescent device using the same |
WO2010031485A1 (en) | 2008-09-22 | 2010-03-25 | Merck Patent Gmbh | Materials for organic electroluminescence devices |
Family Cites Families (106)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5061569A (en) | 1990-07-26 | 1991-10-29 | Eastman Kodak Company | Electroluminescent device with organic electroluminescent medium |
EP0650955B1 (en) | 1993-11-01 | 1998-08-19 | Hodogaya Chemical Co., Ltd. | Amine compound and electro-luminescence device comprising same |
AU681934B2 (en) | 1995-03-14 | 1997-09-11 | Kalford Pty Ltd | A hinge |
US6939625B2 (en) | 1996-06-25 | 2005-09-06 | Nôrthwestern University | Organic light-emitting diodes and methods for assembly and enhanced charge injection |
US6528187B1 (en) | 1998-09-08 | 2003-03-04 | Fuji Photo Film Co., Ltd. | Material for luminescence element and luminescence element using the same |
US6830828B2 (en) | 1998-09-14 | 2004-12-14 | The Trustees Of Princeton University | Organometallic complexes as phosphorescent emitters in organic LEDs |
US6458475B1 (en) | 1999-11-24 | 2002-10-01 | The Trustee Of Princeton University | Organic light emitting diode having a blue phosphorescent molecule as an emitter |
KR100377321B1 (en) | 1999-12-31 | 2003-03-26 | 주식회사 엘지화학 | Electronic device comprising organic compound having p-type semiconducting characteristics |
US20020121638A1 (en) | 2000-06-30 | 2002-09-05 | Vladimir Grushin | Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds |
JP5241053B2 (en) | 2000-08-11 | 2013-07-17 | ザ、トラスティーズ オブ プリンストン ユニバーシティ | Organometallic compounds and radiation-transfer organic electrophosphors |
US6579630B2 (en) | 2000-12-07 | 2003-06-17 | Canon Kabushiki Kaisha | Deuterated semiconducting organic compounds used for opto-electronic devices |
JP3812730B2 (en) | 2001-02-01 | 2006-08-23 | 富士写真フイルム株式会社 | Transition metal complex and light emitting device |
JP4307000B2 (en) | 2001-03-08 | 2009-08-05 | キヤノン株式会社 | Metal coordination compound, electroluminescent element and display device |
JP4310077B2 (en) | 2001-06-19 | 2009-08-05 | キヤノン株式会社 | Metal coordination compound and organic light emitting device |
EP1407501B1 (en) | 2001-06-20 | 2009-05-20 | Showa Denko K.K. | Light emitting material and organic light-emitting device |
US7250226B2 (en) | 2001-08-31 | 2007-07-31 | Nippon Hoso Kyokai | Phosphorescent compound, a phosphorescent composition and an organic light-emitting device |
US7431968B1 (en) | 2001-09-04 | 2008-10-07 | The Trustees Of Princeton University | Process and apparatus for organic vapor jet deposition |
US6835469B2 (en) | 2001-10-17 | 2004-12-28 | The University Of Southern California | Phosphorescent compounds and devices comprising the same |
US7166368B2 (en) | 2001-11-07 | 2007-01-23 | E. I. Du Pont De Nemours And Company | Electroluminescent platinum compounds and devices made with such compounds |
US6863997B2 (en) | 2001-12-28 | 2005-03-08 | The Trustees Of Princeton University | White light emitting OLEDs from combined monomer and aggregate emission |
KR100691543B1 (en) | 2002-01-18 | 2007-03-09 | 주식회사 엘지화학 | New material for transporting electron and organic electroluminescent display using the same |
US7189989B2 (en) | 2002-08-22 | 2007-03-13 | Fuji Photo Film Co., Ltd. | Light emitting element |
KR100686268B1 (en) | 2002-08-27 | 2007-02-28 | 후지필름 가부시키가이샤 | Organometallic Complexes, Organic EL Devices, and Organic EL Displays |
US6687266B1 (en) | 2002-11-08 | 2004-02-03 | Universal Display Corporation | Organic light emitting materials and devices |
JP4365196B2 (en) | 2002-12-27 | 2009-11-18 | 富士フイルム株式会社 | Organic electroluminescence device |
JP4365199B2 (en) | 2002-12-27 | 2009-11-18 | 富士フイルム株式会社 | Organic electroluminescence device |
US7338722B2 (en) | 2003-03-24 | 2008-03-04 | The University Of Southern California | Phenyl and fluorenyl substituted phenyl-pyrazole complexes of Ir |
US7090928B2 (en) | 2003-04-01 | 2006-08-15 | The University Of Southern California | Binuclear compounds |
US7345301B2 (en) | 2003-04-15 | 2008-03-18 | Merck Patent Gmbh | Mixtures of matrix materials and organic semiconductors capable of emission, use of the same and electronic components containing said mixtures |
US7029765B2 (en) | 2003-04-22 | 2006-04-18 | Universal Display Corporation | Organic light emitting devices having reduced pixel shrinkage |
WO2004107822A1 (en) | 2003-05-29 | 2004-12-09 | Nippon Steel Chemical Co., Ltd. | Organic electroluminescent element |
JP2005011610A (en) | 2003-06-18 | 2005-01-13 | Nippon Steel Chem Co Ltd | Organic electroluminescent element |
WO2005007659A2 (en) * | 2003-07-11 | 2005-01-27 | Georgetown University | Diketiminato cu(i) and co(i) carbene catalysts, and cyclopropanation methods using them |
US20050025993A1 (en) | 2003-07-25 | 2005-02-03 | Thompson Mark E. | Materials and structures for enhancing the performance of organic light emitting devices |
TWI390006B (en) | 2003-08-07 | 2013-03-21 | Nippon Steel Chemical Co | Organic EL materials with aluminum clamps |
US20060269780A1 (en) | 2003-09-25 | 2006-11-30 | Takayuki Fukumatsu | Organic electroluminescent device |
JP4822687B2 (en) | 2003-11-21 | 2011-11-24 | 富士フイルム株式会社 | Organic electroluminescence device |
US7332232B2 (en) | 2004-02-03 | 2008-02-19 | Universal Display Corporation | OLEDs utilizing multidentate ligand systems |
WO2005089024A1 (en) | 2004-03-11 | 2005-09-22 | Mitsubishi Chemical Corporation | Composition for charge-transporting film and ion compound, charge-transporting film and organic electroluminescent device using same, and method for manufacturing organic electroluminescent device and method for producing charge-transporting film |
TW200531592A (en) | 2004-03-15 | 2005-09-16 | Nippon Steel Chemical Co | Organic electroluminescent device |
JP4869565B2 (en) | 2004-04-23 | 2012-02-08 | 富士フイルム株式会社 | Organic electroluminescence device |
US7491823B2 (en) | 2004-05-18 | 2009-02-17 | The University Of Southern California | Luminescent compounds with carbene ligands |
US7534505B2 (en) | 2004-05-18 | 2009-05-19 | The University Of Southern California | Organometallic compounds for use in electroluminescent devices |
US7154114B2 (en) | 2004-05-18 | 2006-12-26 | Universal Display Corporation | Cyclometallated iridium carbene complexes for use as hosts |
WO2005123873A1 (en) | 2004-06-17 | 2005-12-29 | Konica Minolta Holdings, Inc. | Organic electroluminescent device material, organic electroluminescent device, display and illuminating device |
CA2568667A1 (en) | 2004-06-28 | 2006-01-05 | Ciba Specialty Chemicals Holding Inc. | Electroluminescent metal complexes with triazoles and benzotriazoles |
US20060008670A1 (en) | 2004-07-06 | 2006-01-12 | Chun Lin | Organic light emitting materials and devices |
JP4858169B2 (en) | 2004-07-23 | 2012-01-18 | コニカミノルタホールディングス株式会社 | Organic electroluminescence device |
DE102004057072A1 (en) | 2004-11-25 | 2006-06-01 | Basf Ag | Use of Transition Metal Carbene Complexes in Organic Light Emitting Diodes (OLEDs) |
EP1859656B1 (en) | 2004-12-30 | 2013-07-17 | E.I. Du Pont De Nemours And Company | Organometallic complexes |
WO2006082742A1 (en) | 2005-02-04 | 2006-08-10 | Konica Minolta Holdings, Inc. | Organic electroluminescent device material, organic electroluminescent device, display and illuminating device |
KR100803125B1 (en) | 2005-03-08 | 2008-02-14 | 엘지전자 주식회사 | Red phosphorescent compounds and organic electroluminescence devices using the same |
WO2006098120A1 (en) | 2005-03-16 | 2006-09-21 | Konica Minolta Holdings, Inc. | Organic electroluminescent device material and organic electroluminescent device |
DE102005014284A1 (en) | 2005-03-24 | 2006-09-28 | Basf Ag | Use of compounds containing aromatic or heteroaromatic rings containing groups via carbonyl groups as matrix materials in organic light-emitting diodes |
JPWO2006103874A1 (en) | 2005-03-29 | 2008-09-04 | コニカミノルタホールディングス株式会社 | ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL, ORGANIC ELECTROLUMINESCENT ELEMENT, DISPLAY DEVICE AND LIGHTING DEVICE |
GB2439030B (en) | 2005-04-18 | 2011-03-02 | Konica Minolta Holdings Inc | Organic electroluminescent device, display and illuminating device |
US7807275B2 (en) | 2005-04-21 | 2010-10-05 | Universal Display Corporation | Non-blocked phosphorescent OLEDs |
US9051344B2 (en) | 2005-05-06 | 2015-06-09 | Universal Display Corporation | Stability OLED materials and devices |
JP4533796B2 (en) | 2005-05-06 | 2010-09-01 | 富士フイルム株式会社 | Organic electroluminescence device |
EP2277978B1 (en) | 2005-05-31 | 2016-03-30 | Universal Display Corporation | Triphenylene hosts in phosphorescent light emitting diodes |
CN101193875B (en) | 2005-06-07 | 2011-05-11 | 新日铁化学株式会社 | Organic metal complex and organic electroluminescent device using same |
WO2007002683A2 (en) | 2005-06-27 | 2007-01-04 | E. I. Du Pont De Nemours And Company | Electrically conductive polymer compositions |
WO2007004380A1 (en) | 2005-07-01 | 2007-01-11 | Konica Minolta Holdings, Inc. | Organic electroluminescent element material, organic electroluminescent element, display device, and lighting equipment |
WO2007028417A1 (en) | 2005-09-07 | 2007-03-15 | Technische Universität Braunschweig | Triplett emitter having condensed five-membered rings |
JP4887731B2 (en) | 2005-10-26 | 2012-02-29 | 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 |
JP4593631B2 (en) | 2005-12-01 | 2010-12-08 | 新日鐵化学株式会社 | Compound for organic electroluminescence device and organic electroluminescence device |
JPWO2007063796A1 (en) | 2005-12-01 | 2009-05-07 | 新日鐵化学株式会社 | Organic electroluminescence device |
US8142909B2 (en) | 2006-02-10 | 2012-03-27 | Universal Display Corporation | Blue phosphorescent imidazophenanthridine materials |
KR20180117719A (en) | 2006-02-10 | 2018-10-29 | 유니버셜 디스플레이 코포레이션 | METAL COMPLEXES OF CYCLOMETALLATED IMIDAZO[1,2-f]PHENANTHRIDINE AND DIIMIDAZO[1,2-A:1',2'-C]QUINAZOLINE LIGANDS AND ISOELECTRONIC AND BENZANNULATED ANALOGS THEREOF |
JP4823730B2 (en) | 2006-03-20 | 2011-11-24 | 新日鐵化学株式会社 | Luminescent layer compound and organic electroluminescent device |
WO2007125714A1 (en) | 2006-04-26 | 2007-11-08 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescence element using the same |
US8076839B2 (en) | 2006-05-11 | 2011-12-13 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
US8563145B2 (en) | 2006-06-02 | 2013-10-22 | Idemitsu Kosan Co., Ltd. | Material containing two or three dibenzofuran groups, dibenzothiophene groups, or a combination thereof, which is operable for organic electroluminescence elements, and organic electroluminescence elements using the material |
EP2055701A1 (en) | 2006-08-23 | 2009-05-06 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivatives and organic electroluminescent devices made by using the same |
JP5589251B2 (en) | 2006-09-21 | 2014-09-17 | コニカミノルタ株式会社 | Organic electroluminescence element material |
EP2080762B1 (en) | 2006-11-09 | 2016-09-14 | Nippon Steel & Sumikin Chemical Co., Ltd. | Compound for organic electroluminescent device and organic electroluminescent device |
KR20120135325A (en) | 2006-11-24 | 2012-12-12 | 이데미쓰 고산 가부시키가이샤 | Aromatic amine derivative and organic electroluminescent element using the same |
US8778508B2 (en) | 2006-12-08 | 2014-07-15 | Universal Display Corporation | Light-emitting organometallic complexes |
US8119255B2 (en) | 2006-12-08 | 2012-02-21 | Universal Display Corporation | Cross-linkable iridium complexes and organic light-emitting devices using the same |
JP5546255B2 (en) | 2007-02-23 | 2014-07-09 | ビーエーエスエフ ソシエタス・ヨーロピア | Metal complexes with electroluminescent benzotriazole |
WO2008132085A1 (en) | 2007-04-26 | 2008-11-06 | Basf Se | Silanes containing phenothiazine-s-oxide or phenothiazine-s,s-dioxide groups and the use thereof in oleds |
WO2009000673A2 (en) | 2007-06-22 | 2008-12-31 | Basf Se | Light emitting cu(i) complexes |
US20090004385A1 (en) * | 2007-06-29 | 2009-01-01 | Blackwell James M | Copper precursors for deposition processes |
KR101577465B1 (en) | 2007-07-05 | 2015-12-14 | 바스프 에스이 | Organic light-emitting diodes comprising carbene-transition metal complex emitters, and at least one compound selected from disilylcarbazoles, disilyldibenzofurans, disilyldibenzothiophenes, disilyldibenzophospholes, disilyldibenzothiophene s-oxides and disilyldibenzothiophene s,s-dioxides |
TW200909558A (en) | 2007-07-07 | 2009-03-01 | Idemitsu Kosan Co | Naphthalene derivative, material for organic electroluminescence device, and organic electroluminescence device using the same |
US20090045731A1 (en) | 2007-07-07 | 2009-02-19 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
TW200909560A (en) | 2007-07-07 | 2009-03-01 | Idemitsu Kosan Co | Organic electroluminescence device and material for organic electroluminescence devcie |
US8779655B2 (en) | 2007-07-07 | 2014-07-15 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
WO2009008311A1 (en) | 2007-07-07 | 2009-01-15 | Idemitsu Kosan Co., Ltd. | Chrysene derivative and organic electroluminescent device using the same |
US8080658B2 (en) | 2007-07-10 | 2011-12-20 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescent element and organic electroluminescent element employing the same |
JP5619418B2 (en) | 2007-07-10 | 2014-11-05 | 出光興産株式会社 | Material for organic electroluminescence device and organic electroluminescence device using the same |
KR20100065302A (en) | 2007-07-27 | 2010-06-16 | 이 아이 듀폰 디 네모아 앤드 캄파니 | Aqueous dispersions of electrically conducting polymers containing inorganic nanoparticles |
KR101630883B1 (en) | 2007-08-08 | 2016-06-15 | 유니버셜 디스플레이 코포레이션 | Benzo-fused thiophene or benzo-fused furan compounds comprising a triphenylene group |
JP2009040728A (en) | 2007-08-09 | 2009-02-26 | Canon Inc | Organometallic complex and organic light-emitting element using the same |
KR101741778B1 (en) | 2007-10-17 | 2017-05-31 | 유디씨 아일랜드 리미티드 | Transition metal complexes comprising bridged carbene ligands and the use thereof in oleds |
US20090101870A1 (en) | 2007-10-22 | 2009-04-23 | E. I. Du Pont De Nemours And Company | Electron transport bi-layers and devices made with such bi-layers |
US7914908B2 (en) | 2007-11-02 | 2011-03-29 | Global Oled Technology Llc | Organic electroluminescent device having an azatriphenylene derivative |
DE102007053771A1 (en) | 2007-11-12 | 2009-05-14 | Merck Patent Gmbh | Organic electroluminescent devices |
KR101353635B1 (en) | 2007-11-15 | 2014-01-20 | 이데미쓰 고산 가부시키가이샤 | Benzochrysene derivative and organic electroluminescent device using the same |
CN101874316B (en) | 2007-11-22 | 2012-09-05 | 出光兴产株式会社 | Organic EL element and solution containing organic EL material |
US8759819B2 (en) | 2007-11-22 | 2014-06-24 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
WO2009085344A2 (en) | 2007-12-28 | 2009-07-09 | Universal Display Corporation | Dibenzothiophene-containing materials in phosphorescent light emitting diodes |
US8221905B2 (en) | 2007-12-28 | 2012-07-17 | Universal Display Corporation | Carbazole-containing materials in phosphorescent light emitting diodes |
US8471248B2 (en) | 2008-02-12 | 2013-06-25 | Basf Se | Electroluminiscent metal complexes with dibenzo[f,h] quinoxalines |
CN101402644B (en) * | 2008-10-31 | 2010-12-01 | 浙江大学 | Production method for metal aza ring carbene complex |
US8580394B2 (en) * | 2009-11-19 | 2013-11-12 | Universal Display Corporation | 3-coordinate copper(I)-carbene complexes |
-
2010
- 2010-11-17 US US12/948,396 patent/US8580394B2/en active Active
- 2010-11-18 KR KR1020127015896A patent/KR101822668B1/en active IP Right Grant
- 2010-11-18 JP JP2012540041A patent/JP2013511532A/en active Pending
- 2010-11-18 TW TW099139776A patent/TWI513796B/en active
- 2010-11-18 CN CN201710567865.XA patent/CN107793437B/en active Active
- 2010-11-18 WO PCT/US2010/057169 patent/WO2011063083A1/en active Application Filing
- 2010-11-18 IN IN5146DEN2012 patent/IN2012DN05146A/en unknown
- 2010-11-18 CN CN201080059525.2A patent/CN102695711B/en active Active
- 2010-11-18 EP EP10832153.0A patent/EP2501707B1/en active Active
-
2013
- 2013-10-22 US US14/060,006 patent/US9773986B2/en active Active
-
2015
- 2015-09-18 JP JP2015185143A patent/JP6656858B2/en active Active
Patent Citations (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4769292A (en) | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
US5247190A (en) | 1989-04-20 | 1993-09-21 | Cambridge Research And Innovation Limited | Electroluminescent devices |
US5703436A (en) | 1994-12-13 | 1997-12-30 | The Trustees Of Princeton University | Transparent contacts for organic devices |
US5707745A (en) | 1994-12-13 | 1998-01-13 | The Trustees Of Princeton University | Multicolor organic light emitting devices |
US5627164A (en) * | 1995-06-13 | 1997-05-06 | Exxon Research And Engineering Company | Pyrazolyl borates complexes-(LAW294) |
US5834893A (en) | 1996-12-23 | 1998-11-10 | The Trustees Of Princeton University | High efficiency organic light emitting devices with light directing structures |
US6013982A (en) | 1996-12-23 | 2000-01-11 | The Trustees Of Princeton University | Multicolor display devices |
US5844363A (en) | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
US6091195A (en) | 1997-02-03 | 2000-07-18 | The Trustees Of Princeton University | Displays having mesa pixel configuration |
US6337102B1 (en) | 1997-11-17 | 2002-01-08 | The Trustees Of Princeton University | Low pressure vapor phase deposition of organic thin films |
US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
US6087196A (en) | 1998-01-30 | 2000-07-11 | The Trustees Of Princeton University | Fabrication of organic semiconductor devices using ink jet printing |
US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
US6294398B1 (en) | 1999-11-23 | 2001-09-25 | The Trustees Of Princeton University | Method for patterning devices |
US6468819B1 (en) | 1999-11-23 | 2002-10-22 | The Trustees Of Princeton University | Method for patterning organic thin film devices using a die |
US20040174116A1 (en) | 2001-08-20 | 2004-09-09 | Lu Min-Hao Michael | Transparent electrodes |
US20030230980A1 (en) | 2002-06-18 | 2003-12-18 | Forrest Stephen R | Very low voltage, high efficiency phosphorescent oled in a p-i-n structure |
US20040192664A1 (en) * | 2003-01-07 | 2004-09-30 | Klaus Kunz | Copper-carbene complexes and their use |
WO2005019373A2 (en) | 2003-08-19 | 2005-03-03 | Basf Aktiengesellschaft | Transition metal complexes comprising carbene ligands serving as emitters for organic light-emitting diodes (oled's) |
US20050258742A1 (en) * | 2004-05-18 | 2005-11-24 | Yui-Yi Tsai | Carbene containing metal complexes as OLEDs |
US20050260446A1 (en) * | 2004-05-18 | 2005-11-24 | Mackenzie Peter B | Cationic metal-carbene complexes |
US20060024522A1 (en) * | 2004-05-18 | 2006-02-02 | Thompson Mark E | Luminescent compounds with carbene ligands |
US7279704B2 (en) | 2004-05-18 | 2007-10-09 | The University Of Southern California | Complexes with tridentate ligands |
US20090140640A1 (en) * | 2004-05-18 | 2009-06-04 | Thompson Mark E | Luminescent compounds with carbene ligands |
JP2007297347A (en) | 2006-05-02 | 2007-11-15 | Ube Ind Ltd | Substituted phenylethynylcopper-nitrogen-containing heterocyclic carbene complex and organic electroluminescent device using the same |
JP2008303152A (en) | 2007-06-05 | 2008-12-18 | Idemitsu Kosan Co Ltd | New copper complex and organic electroluminescent device using the same |
WO2010031485A1 (en) | 2008-09-22 | 2010-03-25 | Merck Patent Gmbh | Materials for organic electroluminescence devices |
Non-Patent Citations (7)
Title |
---|
ARMAROLI, N.; ACCORSI, G.; HOLLER, M.; MOUDAM, O.; NIERENGARTEN, J. F.; ZHOU, Z.; WEGH, R. T.; WELTER, R.: "Highly luminescent Cu-I complexes for light-emitting electrochemical cells", ADVANCED MATERIALS, vol. 18, no. 10, 2006, pages 1313 - 1316 |
BALDO ET AL.: "Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices", NATURE, vol. 395, 1998, pages 151 - 154 |
BALDO ET AL.: "Very high-efficiency green organic light-emitting devices based on electrophosphorescence", APPL. PHYS. LETT., vol. 75, no. 3, 1999, pages 4 - 6 |
HU ET AL.: "Copper Complexes of Nitrogen-Anchored Trpodal N-Heterocyclic Carbene Ligands", J. AM. CHEM. SOC., vol. 125, 2003, pages 12237 - 12245, XP009111843 * |
HU XILE, J. AM. CHEM. SOC., vol. 125, 2003, pages 12237 - 12245 |
See also references of EP2501707A4 |
ZHANG, Q. S.; ZHOU, Q. G.; CHENG, Y. X.; WANG, L. X.; MA, O. G; JING, X. B.; WANG, F. S.: "Highly efficient green phosphorescent organic light-emitting diodes based on Cu-I complexes", ADVANCED MATERIALS, vol. 16, no. 5, 2004, pages 432436 |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102011003192B4 (en) * | 2011-01-26 | 2015-12-24 | Siemens Aktiengesellschaft | Semiconductor component and method for its production |
DE102011003192A1 (en) * | 2011-01-26 | 2012-07-26 | Siemens Aktiengesellschaft | Dopant for organic hole conductors |
US9263696B2 (en) | 2011-01-26 | 2016-02-16 | Siemens Aktiengesellschaft | Organic semiconductor component comprising a doped hole conductor layer |
US9246103B2 (en) | 2011-07-25 | 2016-01-26 | Merck Patent Gmbh | Polymers and oligomers with functionalized side groups |
US9178159B2 (en) | 2011-07-25 | 2015-11-03 | Merck Patent Gmbh | Copolymers with functionalized side chains |
WO2013014066A1 (en) * | 2011-07-26 | 2013-01-31 | Eberhard Karls Universität Tübingen | Complex compounds that comprise a ligand having an n- and a p-donor, and use thereof in the optoelectronic field |
US9553276B2 (en) | 2011-07-26 | 2017-01-24 | Merck Patent Gmbh | Complex compounds having tetradentate ligands and the use thereof in the opto-electronic field |
US9425398B2 (en) | 2011-07-26 | 2016-08-23 | Merck Patent Gmbh | Complex compounds having anionic ligands containing two P donors and the use thereof in the opto-electronic field |
JP2014527292A (en) * | 2011-07-26 | 2014-10-09 | メルク パテント ゲーエムベーハー | Complex compounds comprising anionic ligands with two P-donors and their use in the field of optoelectronics |
JP2014529180A (en) * | 2011-07-26 | 2014-10-30 | メルク パテント ゲーエムベーハー | Complex compounds containing ligands with N and P donors and their use in the field of optoelectronics |
US9082990B2 (en) | 2011-07-26 | 2015-07-14 | Merck Patent Gmbh | Complex compounds having a ligand containing an N donor and a P donor and the use thereof in the opto-electronic field |
US9537117B2 (en) | 2011-08-02 | 2017-01-03 | Cynora Gmbh | Singlet harvesting with dual-core copper (I) complexes for optoelectronic devices |
WO2013017675A1 (en) * | 2011-08-02 | 2013-02-07 | Cynora Gmbh | Singlet harvesting with dual-core copper (i) complexes for optoelectronic devices |
EP2554625A1 (en) * | 2011-08-02 | 2013-02-06 | cynora GmbH | Singlet harvesting with two-core copper(I) complexes for opto-electronic devices |
DE102011084639A1 (en) * | 2011-10-17 | 2013-04-18 | Osram Opto Semiconductors Gmbh | ORGANIC ELECTRONIC COMPONENT WITH DUTY, USE OF A DOPING AGENT AND METHOD FOR PRODUCING THE DUTY |
US9799840B2 (en) | 2011-10-17 | 2017-10-24 | Osram Oled Gmbh | Organic electronic component with dopant, use of a dopant and method for the production of the dopant |
US10158092B2 (en) | 2011-10-17 | 2018-12-18 | Osram Oled Gmbh | Organic electronic component with dopant, use of a dopant and method for the production of the dopant |
EP2623508A1 (en) | 2012-02-02 | 2013-08-07 | Konica Minolta Advanced Layers, Inc. | Iridium complex compound, organic electroluminescent element material, organic electroluminescent element, illumination device and display device |
US8786179B2 (en) | 2012-09-17 | 2014-07-22 | Universal Display Corporation | Light emitting device comprising phosphorescent materials for white light generation |
US10128450B2 (en) | 2013-10-23 | 2018-11-13 | University Of Southern California | Organic electroluminescent materials and devices |
WO2017046572A1 (en) * | 2015-09-14 | 2017-03-23 | University Of East Anglia | Metal complexes |
US10700295B2 (en) | 2015-09-14 | 2020-06-30 | Uea Enterprises Limited | Metal complexes |
Also Published As
Publication number | Publication date |
---|---|
US8580394B2 (en) | 2013-11-12 |
US20120056529A1 (en) | 2012-03-08 |
CN107793437B (en) | 2024-05-24 |
CN102695711B (en) | 2018-03-23 |
JP6656858B2 (en) | 2020-03-04 |
TWI513796B (en) | 2015-12-21 |
JP2013511532A (en) | 2013-04-04 |
US20140125221A1 (en) | 2014-05-08 |
JP2016040270A (en) | 2016-03-24 |
CN102695711A (en) | 2012-09-26 |
IN2012DN05146A (en) | 2015-10-23 |
EP2501707B1 (en) | 2017-08-02 |
TW201134918A (en) | 2011-10-16 |
KR20120085917A (en) | 2012-08-01 |
EP2501707A4 (en) | 2014-03-26 |
CN107793437A (en) | 2018-03-13 |
EP2501707A1 (en) | 2012-09-26 |
US9773986B2 (en) | 2017-09-26 |
KR101822668B1 (en) | 2018-01-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6656858B2 (en) | 3-coordinate copper (I) -carbene complex | |
KR102118826B1 (en) | Cyclometallated tetradentate pt(ii) complexes comprised of one or two imidazole rings with a twisted aryl group bonded to n-1 | |
JP6219466B2 (en) | Phosphorescent substance | |
EP2564438B1 (en) | Depositing premixed materials | |
JP6279632B2 (en) | Delayed fluorescent OLED | |
KR101785755B1 (en) | Azaborine compounds as host materials and dopants for pholeds | |
JP6035076B2 (en) | Materials for organic light emitting diodes | |
EP2565249B1 (en) | Cyclometallated tetradentate Pt (II) complexes | |
WO2012102967A1 (en) | Aza - dibenzothiophene, aza - dibenzofuran and aza - dibenzoselenophene derivatives for use in oled ' s | |
WO2012023947A1 (en) | Bicarbazole compounds for oleds | |
WO2012016074A1 (en) | Co-deposition methods for the fabrication of organic optoelectronic devices | |
KR20210096021A (en) | Organic electroluminescent materials and devices | |
WO2012078453A1 (en) | Capture agents for unsaturated metal complexes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10832153 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2012540041 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 5146/DELNP/2012 Country of ref document: IN |
|
ENP | Entry into the national phase |
Ref document number: 20127015896 Country of ref document: KR Kind code of ref document: A |
|
REEP | Request for entry into the european phase |
Ref document number: 2010832153 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010832153 Country of ref document: EP |