WO2011137922A1 - Formulierungen und elektronische vorrichtungen - Google Patents
Formulierungen und elektronische vorrichtungen Download PDFInfo
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- WO2011137922A1 WO2011137922A1 PCT/EP2010/007176 EP2010007176W WO2011137922A1 WO 2011137922 A1 WO2011137922 A1 WO 2011137922A1 EP 2010007176 W EP2010007176 W EP 2010007176W WO 2011137922 A1 WO2011137922 A1 WO 2011137922A1
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- 239000000203 mixture Substances 0.000 title claims abstract description 84
- 238000009472 formulation Methods 0.000 title claims abstract description 62
- 150000001875 compounds Chemical class 0.000 claims abstract description 154
- 125000003118 aryl group Chemical group 0.000 claims abstract description 93
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 70
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 29
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 24
- 125000005309 thioalkoxy group Chemical group 0.000 claims abstract description 24
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 21
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
- 125000006413 ring segment Chemical group 0.000 claims abstract description 20
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 19
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 19
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 18
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 18
- 239000002904 solvent Substances 0.000 claims abstract description 17
- 125000004104 aryloxy group Chemical group 0.000 claims abstract description 14
- 125000003367 polycyclic group Chemical group 0.000 claims abstract description 14
- 125000002950 monocyclic group Chemical group 0.000 claims abstract description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 12
- 125000005553 heteroaryloxy group Chemical group 0.000 claims abstract description 12
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims abstract description 10
- 239000001257 hydrogen Substances 0.000 claims abstract description 9
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 7
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims abstract description 7
- 125000000468 ketone group Chemical group 0.000 claims abstract description 7
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims abstract description 7
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 5
- 125000005067 haloformyl group Chemical group 0.000 claims abstract description 5
- 125000005843 halogen group Chemical group 0.000 claims abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 5
- NONOKGVFTBWRLD-UHFFFAOYSA-N thioisocyanate group Chemical group S(N=C=O)N=C=O NONOKGVFTBWRLD-UHFFFAOYSA-N 0.000 claims abstract description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 4
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims abstract description 4
- 125000002462 isocyano group Chemical group *[N+]#[C-] 0.000 claims abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 45
- 239000000463 material Substances 0.000 claims description 39
- 238000002347 injection Methods 0.000 claims description 27
- 239000007924 injection Substances 0.000 claims description 27
- 230000005525 hole transport Effects 0.000 claims description 14
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 11
- 125000004429 atom Chemical group 0.000 claims description 9
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- 230000003381 solubilizing effect Effects 0.000 claims description 8
- 230000000903 blocking effect Effects 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims description 5
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- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 108091008695 photoreceptors Proteins 0.000 claims description 3
- 239000010409 thin film Substances 0.000 claims description 3
- 230000007704 transition Effects 0.000 claims description 3
- 238000010791 quenching Methods 0.000 claims description 2
- RICKKZXCGCSLIU-UHFFFAOYSA-N 2-[2-[carboxymethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]ethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]acetic acid Chemical compound CC1=NC=C(CO)C(CN(CCN(CC(O)=O)CC=2C(=C(C)N=CC=2CO)O)CC(O)=O)=C1O RICKKZXCGCSLIU-UHFFFAOYSA-N 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 72
- 239000010410 layer Substances 0.000 description 62
- -1 methylated alicyclic alcohols Chemical class 0.000 description 55
- 150000003254 radicals Chemical class 0.000 description 38
- 230000015572 biosynthetic process Effects 0.000 description 37
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- 238000003786 synthesis reaction Methods 0.000 description 35
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
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- 229910052751 metal Inorganic materials 0.000 description 23
- 239000002184 metal Substances 0.000 description 23
- 229910052760 oxygen Inorganic materials 0.000 description 23
- 229910052717 sulfur Inorganic materials 0.000 description 23
- 229910052741 iridium Inorganic materials 0.000 description 22
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
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- 239000003446 ligand Substances 0.000 description 15
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- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 12
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- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 11
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- 229910052740 iodine Inorganic materials 0.000 description 11
- 125000001424 substituent group Chemical group 0.000 description 11
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 10
- 125000003342 alkenyl group Chemical group 0.000 description 10
- 238000001816 cooling Methods 0.000 description 10
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 10
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 10
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 9
- 125000004122 cyclic group Chemical group 0.000 description 9
- 150000002739 metals Chemical class 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 229910052938 sodium sulfate Inorganic materials 0.000 description 8
- 235000011152 sodium sulphate Nutrition 0.000 description 8
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 7
- DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 description 7
- 239000007983 Tris buffer Substances 0.000 description 7
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 7
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- 150000003384 small molecules Chemical class 0.000 description 7
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 150000001454 anthracenes Chemical class 0.000 description 6
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 6
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 6
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 6
- 229910052698 phosphorus Chemical class 0.000 description 6
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 6
- 229930192474 thiophene Natural products 0.000 description 6
- 125000005259 triarylamine group Chemical group 0.000 description 6
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 6
- UWRZIZXBOLBCON-VOTSOKGWSA-N (e)-2-phenylethenamine Chemical class N\C=C\C1=CC=CC=C1 UWRZIZXBOLBCON-VOTSOKGWSA-N 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- UWRZIZXBOLBCON-UHFFFAOYSA-N 2-phenylethenamine Chemical class NC=CC1=CC=CC=C1 UWRZIZXBOLBCON-UHFFFAOYSA-N 0.000 description 5
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 5
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 5
- 125000005577 anthracene group Chemical group 0.000 description 5
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- 230000008901 benefit Effects 0.000 description 5
- 150000001716 carbazoles Chemical class 0.000 description 5
- 125000005842 heteroatom Chemical group 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 5
- 238000007641 inkjet printing Methods 0.000 description 5
- 150000002576 ketones Chemical class 0.000 description 5
- 229910052744 lithium Inorganic materials 0.000 description 5
- 239000012044 organic layer Substances 0.000 description 5
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical class C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
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- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
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- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 4
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 4
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- 150000001340 alkali metals Chemical group 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
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- VPUGDVKSAQVFFS-UHFFFAOYSA-N coronene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3)C4=C4C3=CC=C(C=C3)C4=C2C3=C1 VPUGDVKSAQVFFS-UHFFFAOYSA-N 0.000 description 4
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- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 4
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
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- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 4
- HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical compound OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 description 4
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- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 4
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- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 4
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- 125000005504 styryl group Chemical group 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 3
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- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 3
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 3
- 229920003026 Acene Polymers 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 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 3
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical class [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
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- 239000000654 additive Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229910001413 alkali metal ion Inorganic materials 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
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- 239000012298 atmosphere Substances 0.000 description 3
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- XOTVOQNSISWTIK-UHFFFAOYSA-N benzo[a]anthracen-4-ylboronic acid Chemical compound C1=CC2=CC3=CC=CC=C3C=C2C2=C1C(B(O)O)=CC=C2 XOTVOQNSISWTIK-UHFFFAOYSA-N 0.000 description 3
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- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
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- GDISDVBCNPLSDU-UHFFFAOYSA-N pyrido[2,3-g]quinoline Chemical compound C1=CC=NC2=CC3=CC=CN=C3C=C21 GDISDVBCNPLSDU-UHFFFAOYSA-N 0.000 description 1
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 description 1
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- 230000005855 radiation Effects 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- FMKFBRKHHLWKDB-UHFFFAOYSA-N rubicene Chemical compound C12=CC=CC=C2C2=CC=CC3=C2C1=C1C=CC=C2C4=CC=CC=C4C3=C21 FMKFBRKHHLWKDB-UHFFFAOYSA-N 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
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- 239000003381 stabilizer Substances 0.000 description 1
- 150000001629 stilbenes Chemical class 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000005092 sublimation method Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 150000001911 terphenyls Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 150000003513 tertiary aromatic amines Chemical class 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- GVIJJXMXTUZIOD-UHFFFAOYSA-N thianthrene Chemical compound C1=CC=C2SC3=CC=CC=C3SC2=C1 GVIJJXMXTUZIOD-UHFFFAOYSA-N 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- NZFNXWQNBYZDAQ-UHFFFAOYSA-N thioridazine hydrochloride Chemical compound Cl.C12=CC(SC)=CC=C2SC2=CC=CC=C2N1CCC1CCCCN1C NZFNXWQNBYZDAQ-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
- 150000005199 trimethylbenzenes Chemical class 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 125000005580 triphenylene group Chemical group 0.000 description 1
- RMNIZOOYFMNEJJ-UHFFFAOYSA-K tripotassium;phosphate;hydrate Chemical compound O.[K+].[K+].[K+].[O-]P([O-])([O-])=O RMNIZOOYFMNEJJ-UHFFFAOYSA-K 0.000 description 1
- YGPLLMPPZRUGTJ-UHFFFAOYSA-N truxene Chemical compound C1C2=CC=CC=C2C(C2=C3C4=CC=CC=C4C2)=C1C1=C3CC2=CC=CC=C21 YGPLLMPPZRUGTJ-UHFFFAOYSA-N 0.000 description 1
- 238000002061 vacuum sublimation Methods 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
- H10K85/1135—Polyethylene dioxythiophene [PEDOT]; Derivatives thereof
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/27—Polycyclic condensed hydrocarbons containing three rings
- C07C15/30—Phenanthrenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/38—Polycyclic condensed hydrocarbons containing four rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/54—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to two or three six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
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Definitions
- the present invention relates to formulations for the manufacture of electronic devices. Furthermore, the present invention relates to electronic devices and methods for their preparation.
- Performance can be used in many commercial products. Examples include organic-based charge transport materials (e.g., triarylamine-based hole transporters) in copiers, organic or polymeric light-emitting diodes (OLEDs or PLEDs), and display and display devices or organic photoreceptors in copiers.
- organic solar cells O-SC
- organic field effect transistors O-FET
- organic thin-film transistors O-TFT
- organic switching elements O-IC
- O-lasers organic laser diodes
- charge injection layer for example, to compensate for unevenness of the electrode (“planarization layer”), often of a conductive, doped polymer,
- a "small molecule OLED” often includes one or more
- small molecules which is based on non-polymeric compounds, is the production of these compounds
- WO 2010/006680 A1 describes organic compounds which are suitable for the production of electronic devices, wherein these compounds can be processed both by vapor deposition and by solution.
- the electronic devices should be used or adapted for many purposes.
- the subject of the present invention is accordingly a
- A is a functional structural element
- B is a solubility-promoting structural element
- k is an integer in the range of 1 to 20,
- the molecular weight of the functional compound is at least 550 g / mol
- Ar 1 , Ar 2 are each independently an aryl or heteroaryl group containing one or more of any R groups
- Nitro group a CF 3 group, Cl, Br, F, a crosslinkable group or a substituted or unsubstituted aromatic or heteroaromatic ring system having 5 to 60 ring atoms, or an aryloxy or heteroaryloxy group having 5 to 60 ring atoms, or a combination of these systems, wherein one or more of R and / or R 2 is a mono - or
- polycyclic, aliphatic or aromatic ring system with each other and / or with the ring to which the group R is bonded, can form;
- I is 0, 1, 2, 3 or 4;
- Structural element indicates.
- a formulation according to the invention is a mixture of at least two functional compounds of the formula (I) which are dissolved or dispersed in an organic solvent.
- a formulation according to the invention comprises at least one organic solvent.
- Suitable and preferred solvents are aliphatic, cycloaliphatic or aromatic hydrocarbons, amines, thiols, amides, nitriles, esters, ethers, polyethers, alcohols, diols and / or polyols.
- the solvent comprises at least one aromatic or heteroaromatic compound.
- the solvent particularly preferably comprises at least one aromatic hydrocarbon and / or one haloaromatic, more preferably at least one
- These include in particular toluene, dimethylbenzene (xylenes), trimethylbenzenes,
- Methylnaphthalenes tetralin, cyclopentylbenzene and cyclohexylbenzene.
- aromatic or heteroaromatic compounds which in the side group heteroatoms, in particular esters, ethers, nitriles and / or amides.
- Preferred compounds of this class include aromatic alkoxy compounds such as 3-methylanisole, 2-isopropylanisole, 5-methoxyindan, 2-ethoxynaphthalene, and aromatic esters such as butyl benzoate and ethyl benzoate.
- heteroaromatic solvents having an O, N or S atom in the aromatic ring, such as 2-methylindole and 6-methylquinoline.
- heterocyclic compounds can be used as a solvent, such as 1-cyclohexyl-2-pyrrolidinone (N-cyclohexyl-pyrrolidinone).
- alcohols are a suitable solvent class.
- the preferred alcohols include in particular alkylcyclohexanols, in particular methylated alicyclic alcohols (3- or 4-methylcyclohexanol or 2,5-dimethylcyclohexanol), naphthols, for example decahydro-2-naphthol or 1,2,3, 4-tetrahydro-1-naphthol, terpenoids such as a-terpineol, menthol or carveol, nonylphenol, 1-indanol and 2-indanol.
- cycloalkanes can be used as solvents, such as decalin.
- the solvents may be used singly or as a mixture of two, three or more compounds.
- the preferred solvents include, but are not limited to, toluene, anisole, xylenes, methyl benzoate, dimethylanisoles, mesitylenes, tetralin, veratrole, tetrahydrofuran and chlorobenzene, and mixtures thereof.
- aromatic solvents in particular aromatic hydrocarbons.
- a formulation according to the invention may comprise at least 50% by weight, more preferably at least 80% by weight and most preferably at least 90% by weight of aromatic solvent.
- H d (dispersing fraction) in the range of 17.0 to 23.2 MPa 0.5 , more preferably in the range of 18.5 to 21, 0 MPa 0.5 ;
- H p (polar contribution) in the range of 0.2 to 12.5 MPa 0.5 , more preferably in the range of 2.0 to 6.0 MPa 0 ' 5 and
- H h hydrogen bonding contribution in the range from 0.9 to 14.2 MPa 0.5 , particularly preferably in the range from 2.0 to 6.0 MPa 0.5 .
- the solubility parameters according to Hansen can be determined with the computer program "the Hansen Solubility Parameters in Practice (HSPiP) program (2 nd edition)", which is described by Hanson and Abbot et al.
- Preferred functional compounds according to formula (I) may have two, three or more of the solubilizing structural elements B. Accordingly, the index k in formula (I) may preferably be an integer greater than or equal to 2, more preferably greater than or equal to 3.
- preferred functional compounds of the general formula (I) are distinguished by a molecular weight of at least 800 g / mol, particularly preferably at least 900 g / mol and very particularly preferably at least 950 g / mol.
- preferred functional compounds of the formula (I) may have a molecular weight of at most 10,000 g / mol, more preferably from at most 5000 g / mol, and most preferably at most 3000 g / mol.
- the functional structural element A of the functional compound of formula (I) is not subject to any particular limitation, so that the present invention is suitable, known substances that are used in electronic
- Devices are used to achieve functional properties to convert to a soluble form, without thereby changing the original electronic properties of the known substances in an unacceptable manner.
- the functional structural elements A can originate, for example, from the following classes:
- Group 1 units, the hole injection and / or
- Group 3 units which have light-emitting properties
- Group 4 units that can serve as host materials or co-host materials
- Group 5 units that improve the transition from the so-called singlet to triplet state.
- Have hole transport properties are, for example, triarylamine, benzidine, tetraaryl-para-phenylenediamine, triarylphosphine, phenothiazine, phenoxazine, dihydrophenazine, thianthrene, dibenzo-para-dioxin,
- group 1 structural elements which have hole injection and / or hole transport properties
- Phenylenediamine derivatives (US 3615404), arylamine derivatives (US 3567450), amino-substituted chalcone derivatives (US 3526501), styrylanthracene derivatives (JP-A-56-46234), polycyclic aromatic compounds (EP 1009041), polyarylalkane Derivatives (US 3615402), fluorenone derivatives (JP-A-54-110837), hydrazone derivatives (US 3717462), acylhydrazones, stilbene derivatives (JP-A-61-210363), silazane derivatives (US 4950950), Polysilanes (JP-A-2-204996), aniline copolymers (JP-A-2-282263), thiophene oligomers (JP Heisei 1 (1989) 211399), polythiophenes, poly (N-vinylcarbazole) (PVK), polypyrroles , Polyanilines and other electroconductive macromolecule
- Arylamine dendrimers can also be used (JP Heisei 8 (1996) 193191), monomeric triarylamines (US 3180730), triarylamines having one or more vinyl radicals and / or at least one active hydrogen functional group (US 3567450 and US 3658520) or tetraaryldiamines (the two tertiary amino units are via an aryl group connected). There may also be more triarylamino groups in the molecule. Also phthalocyanine derivatives,
- Naphthalocyanine derivatives, butadiene derivatives and quinoline derivatives such as e.g. Dipyrazino [2,3-f: 2 ', 3'-h] quinoxaline-hexacarbonitrile are suitable.
- aromatic tertiary amines having at least two
- NPD NPD
- TBDB N, N, N ', N'-tetra (4-biphenyl) diaminobiphenylene
- TAPC 1, 1-bis (4-di-p-tolylaminophenyl) cyclohexane
- TAPPP 1,1-bis (4-di-p-
- NPB 4,4'-bis [N- (1-naphthyl) -N-phenylamino] biphenyl
- JP 08292586 Further structural elements which can be used as hole injection materials are described in EP 0891121 A1 and EP 1029909 A1, injection layers generally in US 2004/0174116 A1.
- these arylamines and heterocycles which in the
- group 1 generally used as structural elements of group 1, to a HOMO in the polymer of more than -5.8 eV (against vacuum level), more preferably of more than -5.5 eV.
- Group 2 structural elements having electron injection and / or electron transport properties include, for example, pyridine, pyrimidine, pyridazine, pyrazine, oxadiazole, quinoline, quinoxaline,
- Anthracene, benzanthracene, pyrene, perylene, benzimidazole, triazine, ketone, phosphine oxide and phenazine derivatives, but also triarylboranes and other O-, S- or N-containing heterocycles with low lying LUMO (LUMO lowest unoccupied molecular orbital).
- Particularly suitable structural elements for electron-transporting and electron-injecting layers are metal chelates of 8-hydroxyquinoline (eg LiQ, AlQ 3 , GaQ 3 , MgQ 2 , ZnQ 2 , InQ 3 , ZrQ 4 ), BAIQ, Ga-oxinoid complexes, 4-azaphenanthrene-5 -ol-Be complexes (US 5529853 A),
- 8-hydroxyquinoline eg LiQ, AlQ 3 , GaQ 3 , MgQ 2 , ZnQ 2 , InQ 3 , ZrQ 4
- BAIQ Ga-oxinoid complexes
- 4-azaphenanthrene-5 -ol-Be complexes US 5529853 A
- Butadiene derivatives (US 4356429), heterocyclic optical brighteners (US 4539507), benzimidazole derivatives (US 2007/0273272 A1), such as, for example, TPBI (US Pat. No. 5,761,779),
- 1, 3,5-triazines e.g. Spirobifluorene-triazine derivatives (eg according to DE 102008064200), pyrenes, anthracenes, tetracenes, fluorenes, spirofluorenes, dendrimers, tetracenes (eg rubrene derivatives), 1, 10-phenanthroline derivatives (JP 2003-115387, JP 2004-311184 , JP-2001-267080, WO 2002/043449), sila-cyclopentadiene derivatives (EP 1480280, EP 1478032, EP 1469533), borane derivatives such as Triaryl borane derivatives with Si,
- phenanthrolines especially 1, 10 phenanthroline derivatives, such as BCP and Bphen, also several connected via biphenyl or other aromatic groups phenanthrolines (US 2007-0252517 A1) or anthracene-related phenanthrolines ( US 2007-0122656 A1).
- heterocyclic organic compounds e.g. Thiopyrandioxides, oxazoie, triazoles, imidazoles or oxadiazoles.
- heterocyclic organic compounds e.g. Thiopyrandioxides, oxazoie, triazoles, imidazoles or oxadiazoles.
- examples of the use of five-membered rings with N e.g. Oxazoie, thiazoles, oxadiazoles, thiadiazoles, triazoles and the like. see US 2008/0102311 A1.
- Preferred compounds are as follows:
- Triazoles e.g.
- organic compounds such as derivatives of fluorenone, fluorenylidene methane, perylenetetracarbonic acid, anthraquinonedimethane, diphenoquinone, anthrone and anthraquinone diethylenediamine.
- the structural elements of group 2 in a compound according to formula (I) to be used according to the invention lead to a LUMO of less than -2.5 eV (against vacuum level), more preferably of less than -2.7 eV.
- Group 3 structural elements are those which can emit light. These include compounds with stilbene,
- Stilbeneamine styrylamine, coumarin, rubrene, rhodamine, thiazole, thiadiazole, cyanine, thiophene, paraphenylene, perylene, phatolocyanine, porphyrin, ketone, quinoline, imine, anthracene and / or pyrene structures.
- Particular preference is given to compounds which, even at room temperature, can emit light from the triplet state with high efficiency, ie exhibit electrophosphorescence instead of electrofluorescence, which frequently causes an increase in energy efficiency.
- Compounds which contain heavy atoms with an atomic number of more than 36 are suitable for this purpose.
- Preferred structural elements from group 3 are selected from the class of monostyrylamines, distyrylamines, tristyrylamines, tetrastyrylamines, styrylphosphines, styryl ethers and arylamines
- a monostyrylamine is meant a compound having a substituted or unsubstituted styryl group and at least one, preferably contains aromatic, amine.
- a distyrylamine is understood as meaning a compound which contains two substituted or unsubstituted styryl groups and at least one, preferably aromatic, amine.
- a tristyrylamine is understood as meaning a compound which contains three substituted or unsubstituted styryl groups and at least one, preferably aromatic, amine.
- Under a tetrastyrylamine is a
- Styryl tendency and at least one, preferably aromatic, amine.
- the styryl groups are particularly preferred stilbenes, which may also be further substituted.
- Corresponding phosphines and ethers are defined in analogy to the amines. Under an aryl amine or an aromatic amine in the context of the present invention is a
- At least one of these aromatic or heteroaromatic ring systems is preferably a fused ring system, preferably having at least 14 aromatic ring atoms.
- Preferred examples of these are aromatic anthraceneamines, aromatic
- Anthracenediamines aromatic pyrenamines, aromatic pyrenediamines, aromatic chrysenamines or aromatic chrysendiamines.
- aromatic anthracene amine is meant a compound in which a diarylamino group is bonded directly to an anthracene group, preferably in the 9-position.
- An aromatic anthracenediamine is understood to mean a compound in which two diarylamino groups are bonded directly to an anthracene group, preferably in the 2,6- or 9,10-position.
- Aromatic pyrenamines, pyrenediamines, chrysenamines and chrysenediamines are defined analogously thereto, the diarylamino groups on the pyrene preferably being bonded in the 1-position or in the 1, 6-position.
- indenofluorenamines or -diamines for example according to the WO 06/122630, Benzoindenofluorenaminen or diamines, for example according to WO 08/006449, and Dibenzoindenofluorenaminen or diamines, for example according to WO 07/140847.
- Examples of structural elements of group 3 from the class of styrylamines are substituted or unsubstituted tristilbenamines or the dopants described in WO 06/000388, WO 06/058737, WO
- Particularly preferred styrylamine structural elements of group 3 are:
- triarylamine structural elements of group 3 are:
- JP 08/053397 A and US 6251531 B1 derivatives in EP 1957606 A1 and US 2008/0113101 A1.
- group 3 is selected from derivatives of naphthalene, anthracene, tetracene, benzanthracene,
- Periflanthene indenoperylene, phenanthrene, perylene (US 2007/0252517 A1), pyrene, chrysene, decacyclene, coronene, tetraphenylcyclopentadiene, pentaphenylcyclopentadiene, fluorene, spirofluorene, rubrene, coumarin (US Pat. No. 4,769,292, US Pat. No.
- anthracene compounds are particularly preferably in 9,10- position substituted anthracenes such as 9,10-diphenylanthracene and 9,10-bis (phenylethynyl) anthracene. Also, 1,4-bis (9'-ethynylanthracenyl) benzene is a preferred dopant.
- DMQA ⁇ , ⁇ '-dimethylquinacridone
- DCM 4- (dicyanoethylene) -6- (4-dimethylamino-styryl-2-methyl) -4H-pyran
- thiopyran polymethine, pyrylium and
- Blue fluorescence emitters are preferably polyaromatics, e.g. 9,10-di (2-naphthylanthracene) and other anthracene derivatives, derivatives of tetracene, xanthene, perylene, e.g. 2,5,8,11-tetra-f-butyl-perylene,
- Phenylene e.g. 4,4 '- (bis (9-ethyl-3-carbazovinylene) -1, 1'-biphenyl, fluorene, fluoranthene, arylpyrene (US 2006/0222886 A1), arylenevinylenes (US 5121029, US 5130603), bis (azinyl) imine-boron compounds (US
- phosphorescent emitters can be found in WO 00/70655, WO 01/41512, WO 02/02714, WO 02/15645, EP 1191613, EP 1 91612, EP 1191614 and WO 05/033244.
- Phosphorescent metal complexes preferably contain Ir, Ru, Pd, Pt, Os or Re.
- Preferred ligands are 2-phenylpyridine derivatives, 7,8-benzoquinoline derivatives, 2- (2-thienyl) pyridine derivatives, 2- (1-naphthyl) pyridine derivatives, 1-phenylisoquinoline derivatives, 3-phenylisoquinoline derivatives or 2-phenylquinoline derivatives. All of these compounds may be substituted, e.g. for blue with fluorine, cyano and / or trifluoromethyl substituents.
- Auxiliary ligands are preferably acetylacetonate or picolinic acid.
- Bipyridyl or phenanthroline ligands (Ma et al., Synth. Metals 94, 1998, 245).
- Other tridentate ligand phosphorescent emitters are described in US 6824895 and US 10/729238. Red-emitting phosphorescent complexes can be found in US 6835469 and US 6830828.
- Particularly preferred structural elements which are used as phosphorescent dopants are:
- Group 4 structural elements used as host materials, in particular together with emissive compounds, include materials of various classes.
- Preferred structural elements from group 4, which are used in particular together with fluorescent dopants are selected from the classes of oligoarylenes (for example 2,2 ', 7,7'-tetraphenyl-spirobifluorene according to EP 676461 or dinaphthylanthracene), in particular the oligoarylenes containing condensed aromatic groups such as Anthracene, benzanthracene, benzphenanthrene (DE 10 2009 005746, WO 09/069566), phenanthrene, tetracene, coronene, chrysene, fluorene,
- oligoarylenes for example 2,2 ', 7,7'-tetraphenyl-spirobifluorene according to EP 676461 or dinaphthylanthracene
- the oligoarylenes containing condensed aromatic groups such as Anthracene, benzanthracene, benzphenanthrene (DE 10
- the electron-conducting compounds in particular ketones, phosphine oxides, sulfoxides, etc. (eg according to WO 05/084081 and WO 05/084082), the atropisomers (eg according to WO 06/048268), the Boronic acid derivatives (eg according to WO 06/117052) or the
- Benzanthracenes (e.g., according to WO 08/145239).
- Particularly preferred structural elements of group 4 are selected from the classes of oligoarylenes containing anthracene, benzanthracene and / or pyrene or atropisomers of these compounds.
- an oligoarylene is to be understood as meaning a compound in which at least three aryl or arylene groups are bonded to one another.
- Preferred host materials are selected in particular
- the group Ar 4 is anthracene, which may be substituted by one or more radicals R 1 , and the groups Ar 3 and Ar 5 are attached in positions 9 and 10.
- at least one of Ar 3 and / or Ar 5 is a fused aryl group selected from 1- or 2-naphthyl, 2-, 3- or 9-phenanthrenyl or 2, 3, 4, 5, 6- or 7- benzanthracenyl, which may each be substituted by one or more radicals R 1 .
- Anthracene-based compounds are described in US 2007/0092753 A1 and US 2007/0252517 A1, eg 2- (4- Methylphenyl) -9,10-di- (2-naphthyl) anthracene, 9- (2-naphthyl) -10- (1, 1'-biphenyl) anthracene and 9,10-bis [4- (2,2-diphenylethenyl ) phenyl] anthracene, 9,10-diphenylanthracene, 9,10-bis (phenylethynyl) anthracene and 1,4-bis (9'-ethynylanthracenyl) benzene.
- Further preferred compounds are derivatives of arylamine, styrylamine, fluorescein, diphenylbutadiene, tetraphenylbutadiene, cyclopentadienes, tetraphenylcyclopentadiene, pentaphenylcyclopentadiene, coumarin,
- Oxadiazole bisbenzoxazoline, oxazole, pyridine, pyrazine, imine, benzothiazole, benzoxazole, benzimidazole (US 2007/0092753 A1), e.g.
- TNB 4,4'-bis [N- (1-naphthyl) -N- (2-naphthyl) amino] biphenyl.
- Metal oxinoid complexes such as LiQ or AlQ 3 can be used as co-hosts.
- Group 4 structural elements include materials used with phosphorescent emitters. These structural elements include CBP (N, N-biscarbazolylbiphenyl), carbazole derivatives (eg according to WO 05/039246, US 2005/0069729, JP 2004/288381, EP 1205527 or WO 08/086851), azacarbazoles (eg according to EP 1617710, EP 1617711 , EP 1731584, JP 2005/347160), ketones (eg according to WO 04/093207 or according to DE 102008033943),
- CBP N, N-biscarbazolylbiphenyl
- carbazole derivatives eg according to WO 05/039246, US 2005/0069729, JP 2004/288381, EP 1205527 or WO 08/086851
- azacarbazoles eg according to EP 1617710, EP 1617711 , EP 1731584, JP 2005/347160
- ketones eg
- Phosphine oxides eg according to WO 05/003253
- Oligophenylenes eg according to US 2005/0069729
- bipolar matrix materials eg according to WO 07/137725
- silanes eg
- 9,9-diarylfluorene derivatives for example according to DE 102008017591
- azaboroles or boronic esters e.g.
- Particularly preferred structural elements according to group 4 for the preparation of the matrix for phosphorescent dopants are:
- Compounds which can serve as host material are in particular preferred substances whose functional structural element A has at least one nitrogen atom. These include preferably aromatic amines, triazine and carbazole derivatives. In particular, carbazole derivatives show a surprisingly high efficiency. Triazine derivatives unexpectedly lead to high lifetimes of electronic devices with said compounds.
- Group 5 structural elements are those which enhance the singlet to triplet state transition and which, in support of the Group 3 functional structural elements,
- Carbazole and bridged carbazole dimer units are particularly suitable for this purpose, as are described, for example, in US Pat. in WO 04/070772 A2 and WO 04/113468 A1. Also suitable for this purpose are ketones, phosphine oxides, sulfoxides, sulfones, silane derivatives and similar compounds, as described, for example, in US Pat. in WO 05/040302 A1.
- the functional structural elements A set out above can preferably be bonded to at least one solubility-promoting structural element B via an aromatic and / or heteroaromatic group.
- the binding site is generally not critical so that one or more bonds are present to at least one of the solubilizing structural elements B described below, but which, for reasons of clarity, are not set forth in the formulas set forth above.
- the functional structural elements A set out above can be connected to one or more solubilizing structural elements B via a carbon atom of an aromatic or heteroaromatic ring system.
- a compound according to the invention comprises at least one solubility-imparting structural element B according to formula (L-1)
- Ar 1 , Ar 2 are each independently an aryl or heteroaryl group which may be substituted by one or more arbitrary R groups,
- Each X is independently N or CR 2 , preferably CH, R 1 , R 2 are each independently of one another hydrogen, a straight-chain one
- R 1 and / or R 2 may form a mono- or polycyclic, aliphatic or aromatic ring system with each other and / or with the ring to which the group R 1 is attached;
- I is 0, 1, 2, 3 or 4;
- Structure element A indicates.
- the solubility-imparting structural element B may preferably correspond to the general formula (L-II)
- R, R 2 , R 3 , R 4 are each independently hydrogen, one
- I is 0, 1, 2, 3 or 4
- n 0, 1, 2 or 3 and
- n, o are each independently 0, 1, 2, 3, 4 or 5;
- Structural element indicates.
- the particularly preferred solubilizing structural elements B include inter alia the structural elements of the following formulas:
- Ring atoms which may be substituted by any desired radicals R and which may be linked via any desired positions on the aromatic or heteroaromatic ring, are understood in particular to mean groups derived from benzene, naphthalene, anthracene, phenanthrene, pyrene, chrysene, perylene , Fluoranthene, naphthacene, pentacene, benzopyrene, biphenyl, biphenylene, terphenyl, terphenyls, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis or trans indenofluorene, truxene, isotruxene, spirotruxene, spiroisotruxene, furan, benzofuran, isobenzofuran, dibenzofuran, Thiophene, benzothiophene, isobenzo
- Phenanthrene, dihydrophenanthrene and carbazole Phenanthrene, dihydrophenanthrene and carbazole.
- an aryl group contains 5 to 60 C atoms
- a heteroaryl group in the context of the present invention contains 2 to 60 C atoms and at least one heteroatom, with the proviso that the sum of C atoms and heteroatoms gives at least 5
- the heteroatoms are preferably selected from N, O and / or S.
- an aryl group or heteroaryl group is either a simple aromatic cycle, ie benzene, or a simple heteroaromatic cycle, for example pyridine, pyrimidine, thiophene, or a fused aryl group or heteroaryl group, for example, naphthalene, anthracene, phenanthrene, quinoline, isoquinoline, benzothiophene, benzofuran and indole.
- the structural units of the general formulas (L-I) or (L-II) can, as stated above, contain one or more crosslinkable groups.
- Crosslinkable group means a functional group capable of irreversibly reacting to form a cross-linked material that is insoluble Crosslinking can usually be assisted by heat or by UV, microwave, X-ray or electron beam radiation In this connection, there is little by-product formation in the crosslinking process and, in addition, the crosslinkable groups which form in the
- crosslinkable groups are units containing a double bond, a triple bond, a precursor capable of in situ formation of a double or triple bond, or a heterocyclic addition polymerizable radical.
- radicals methyl, ethyl, n are preferably substituted by an alkyl group having 1 to 40 carbon atoms, in which individual H atoms or CH.sub.1 groups may also be substituted by the abovementioned groups or radicals R.
- An alkoxy group having 1 to 40 carbon atoms is preferably understood as meaning methoxy, trifluoromethoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, s-butoxy, t-butoxy and 2-methylbutoxy.
- the weight ratio of structural element A to structural element B in formula (I) is preferably in the range from 2: 1 to 1:20 and particularly preferably in the range from 1: 1 to 1: 3.
- functional compounds of formula (I) can be carried out using known methods, wherein starting materials are reacted with reactive groups.
- These reactive starting materials comprise the above-described structural units of the above formulas and at least one leaving group in each case, such as, for example, bromine, iodine, boronic acid or boronic acid esters.
- Suitable reactions for the formation of C-C bonds are known to the person skilled in the art and described in the literature. Particularly suitable and preferred coupling reactions, all leading to C-C linkages, are those according to SUZUKI, YAMAMOTO, SILENCE, HECK, NEGISHI, SONOGASHIRA and HIYAMA.
- DCy is the same or different at each occurrence, a cyclic one
- CCy is the same or different at each occurrence as a cyclic group containing a carbon atom through which the cyclic group is bonded to the metal and which in turn may carry one or more substituents R 10 ; is identical or different at each occurrence a mononionic, bidentate chelating ligand, preferably a Diketonatligand;
- ring systems between a plurality of radicals R 10 there may also be a bridge between the groups DCy and CCy.
- a bridge between two or three ligands CCy-DCy or between one or two ligands CCy-DCy and the ligand A can also be present, so that it is a polydentate or polypodal ligand. system acts.
- radicals R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 , R 21 , R 22 and R 23 are each independently hydrogen, a straight-chain alkyl, alkoxy or
- R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 9 , R 20 , R 21 , R 22 and / or R 23 is a mono- or polycyclic, aliphatic or aromatic ring system with each other and / or with the
- each pair of R 12 and R 13 , R 13 and R 14 , R 14 and R 15 , R 18 and R 19 , R 19 and R 20 , R 20 and R 21 independently form optionally saturated or unsaturated C4-C40 ring, which may be interrupted by one or more oxygen and / or sulfur atoms or a group of the formula -N (R a ) -
- R a is a hydrogen atom or an optionally substituted one
- Hydrocarbon group wherein the ring may be optionally substituted
- one or more carbon atoms of the polyacene backbone 5 may optionally be substituted by one or more heteroatoms selected from N, P, As, O, S, Se and Te; and wherein one or more of the substituents R 12 to R 23 attached to adjacent ring positions of the
- Polyacens may together form another saturated or IQ unsaturated ring which may be interrupted by one or more oxygen and / or sulfur atoms or a group of the formula -N (R a ) -, wherein R a represents a hydrogen atom or an optionally substituted one Hydrocarbon group, or an aromatic ring system bonded to the polyacene; and
- n is 0, 1, 2, 3 or 4, preferably 0, 1 or 2, particularly preferably 0 or 2; where at least one of the radicals R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 , R 2 , R 22 and / or R 23 is at least one group of the formula (Ll) or (L-II).
- n in formula (V-II) is 2, this compound represents a pentacene compound.
- the compound may be a "pseudopentacene compound”.
- the present invention provides formulations with functional compounds of general formula (V-IIIa) and / or (V-IIb)
- V-1 IIa (V-1 IIb) where the following applies to the symbols and indices:
- C is when the group Y is bound to a group X 2 , or is the same or different at each occurrence CR or N, when the group Y is not bound to X 2 group;
- E is the same or different covalent at each occurrence
- X 2 is the same or different at each occurrence as a bivalent
- X 3 is the same or different at each occurrence as a bivalent
- q 1, 2, 3, 4, 5 or 6;
- Q is a crosslinkable group or an aromatic or heteroaromatic group having 5 to 40 ring atoms, each of which may be substituted by one or more radicals R 26 , or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, each by one or more
- R may be substituted, or an aryloxy or
- Heteroaryloxy group having 5 to 40 aromatic ring atoms may be substituted by one or more radicals R, or a combination of these systems; two or more substituents R 24 may also together, together with the atoms to which they are attached or, when they are bonded to Ar, form with Ar a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system;
- R 26 - may be replaced and wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or aryl amines, or substituted or unsubstituted carbazoles, each containing one or more R 26 may be substituted, or an aryl or heteroaryl group having 5 to 40 ring atoms, which may be substituted by one or more aromatic or heteroaromatic or by non-aromatic radicals R 27 or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms which may be substituted by one or more non-aromatic radicals R 26 , or an aryloxy or heteroaryloxy group having from 5 to 40 aromatic ring atoms which may be substituted by one or more non-aromatic radicals R 27 , or a combination of these systems; two or more substituents R 25 , together with the atoms to which they are attached, may also together form a mono- or polycyclic, aliphatic, aromatic
- Ar 4 is the same or different at each occurrence, an aromatic or heteroaromatic ring system having 5 to 40 ring atoms, which may be substituted by one or more radicals R 25 ;
- an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may be substituted with one or more radicals R 30 ;
- H is identical or different at each occurrence H, D or an aliphatic, aromatic and / or heteroaromatic hydrocarbon radical having 1 to 20 carbon atoms, in which H atoms may also be replaced by D or F; two or more adjacent substituents R 30 may also together form a mono- or polycyclic, aliphatic or aromatic ring system;
- the complex of formula (VV) is present in monomeric form, as shown above, or that it is in the form of aggregates, for example of two alkali metal ions and two ligands, four alkali metal ions and four ligands, six alkali metal ions and six ligands or in the form of other aggregates.
- Preferred compounds of the formula (V-V) are the compounds of the following formulas (V-V1) and (V-V2),
- Formula (V-V1) Formula (V-V2) wherein the symbols used have the same meaning as previously described for the formulas (V-Ia), (V-Ib), (V-Ic) and (V-Id) and above for the formula (VV), and m is the same or is different for each occurrence of 0, 1, 2 or 3 and o is the same or different at each occurrence for 0, 1, 2, 3 or 4.
- the alkali metal is preferably selected from lithium, sodium and potassium, particularly preferably from lithium and sodium, and is very particularly preferably lithium.
- M lithium.
- CR 7 CR 7 Ar, CN, NO 2 , Si (R 8 ) 3 , B (OR 8 ) 2 , B (R 8 ) 2 , B (N (R 8 ) 2 ) 2 , OSO 2 R 8 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 carbon atoms, each of which may be substituted by one or more radicals R 8 , wherein a or several non-adjacent CH 2 groups
- H is identical or different at each occurrence H, D or an aliphatic, aromatic and / or heteroaromatic hydrocarbon radical having 1 to 20 carbon atoms, in which H atoms may be replaced by F; and
- X is the same or different CR 9 or N at each occurrence
- R 5 has the meaning previously given in relation to formula (V-Vla);
- R 7 has the meaning previously given in relation to formula (V-Vla);
- the particularly preferred functional compounds of the formula (I) include inter alia
- the functional compounds may comprise different functional structural elements A.
- mixtures which have at least one functional compound in which the functional structural element A in formula (I) is a unit which has light-emitting properties and at least one functional compound in which the functional
- Structural element A in formula (I) is a unit which can serve as host material.
- the mixture contains at least one functional compound in which the functional
- Structural element A in formula (I) is a unit having light-emitting properties, and at least one functional compound in which the functional structural element A in formula (I) is a unit which can serve as a hole-transporting material.
- the mixture contains at least one functional compound in which the functional
- Structural element A in formula (I) is a unit which is light-emitting Having properties, and at least one functional compound in which the functional structural element A in formula (I) is a unit which can serve as electron transport material.
- the mixture contains at least one functional compound in which the functional
- Structural element A in formula (I) is a unit having light-emitting properties, at least one functional compound in which the functional structural element A in formula (I) is a unit which can serve as a hole-transporting material, and at least one functional compound in which the functional structural element A in formula (I) is a unit which can serve as electron transport material.
- the mixture contains at least one functional compound in which the functional
- Structural element A in formula (I) is a unit which as
- Hole transport material and at least one functional compound in which the functional structural element A in formula (I) is a unit which can serve as electron transport material.
- the proportion by weight of the at least one functional compound in which the functional structural element A in Formula (I) is a unit which can serve as a host material based on all functional compounds in the formulation preferably in the range of 60 to 98 wt .-%, particularly preferably in the range of 70 to 97 wt .-% and in particular in the range from 75 to 95% by weight.
- the weight fraction of functional compound in which the functional structural element A in formula (I) is a unit which has light-emitting properties based on all functional compounds in the formulation but also preferably in the range of 0.01 to 5 wt .-%, more preferably in the range of 0.05 to 3 wt .-% and in particular in the range of 0.1 to 2 wt .-% are. Accordingly, in this embodiment, the
- mixtures can be used, whose
- Structure elements A show the same functionalities.
- the preferred mixtures of this type include in particular formulation with
- Structural element A in formula (I) is a unit which can serve as a host material.
- mixtures which contain at least three functional compounds of the formula (I), where at least two functional compounds have identical functionalities and at least one functional compound comprises a functionality which is different from the first.
- Particularly preferred is in particular a mixture with at least two functional compounds in which the functional structural element A in formula (I) is a unit which can serve as a host material, and at least one functional compound in which the functional structural element A in formula (I) is a unit which has light-emitting properties
- the formulation according to the invention may also comprise functional compounds which contain no solubilizing structural elements. However, these formulations often show a lower
- compositions exclusively functional compounds according to formula (I) included. Accordingly, surprising advantages can be achieved, in particular, by formulations whose proportion of functional compounds which do not comprise solubility-imparting structural element B of the general formula (III) preferably at most 80% by weight, particularly preferably at most 50% by weight and very particularly preferably at most 10 Wt .-%, based on the total weight of the functional compounds.
- the formulation according to the invention can not comprise a functional compound which does not contain a solubility-imparting structural element, so that the formulation consists essentially of solvents, functional compounds of the formula (I) and additives.
- formulations may be excluded which
- Formulation include further additives and processing aids.
- surfactants include, but are not limited to, surfactants, surfactants, lubricants and lubricants, conductivity enhancing additives, dispersants, hydrophobizing agents, coupling agents, flow improvers, defoamers, deaerators, diluents that may be reactive or unreactive, fillers, auxiliaries, processing aids, dyes, Pigments, stabilizers, sensitizers, nanoparticles and inhibitors.
- Compounds containing the structural units according to the invention are used, for example, for producing OLEDs or other electronic devices, preferably as hole transport, hole injection, emitter, electron transport, electron injection, charge blocking and / or charge generation layer.
- the production of the functional layers can be achieved, for example, by coating from solution, preferably spin coating or by any desired printing process, such as screen printing, flexographic printing or offset printing. pressure, but particularly preferably LITI (Light Induced Thermal Imaging, thermal transfer printing) or ink jet printing (ink jet printing).
- LITI Light Induced Thermal Imaging, thermal transfer printing
- ink jet printing ink jet printing
- the present invention also relates to the use of the functional compound in an organic electronic device.
- the organic electronic device is preferably an organic electroluminescent device (OLED), a polymer electroluminescent device (PLED), an organic integrated circuit (O-IC), an organic field effect transistor (O-FET), an organic one Thin film transistor (O-TFT), an organic light emitting transistor (O-LET), an organic solar cell (O-SC), an organic optical detector, an organic photoreceptor, an organic field quench device (O-FQD), a light-emitting electrochemical cell (LEC) or an organic laser diode (O-laser).
- OLED organic electroluminescent device
- PLED polymer electroluminescent device
- O-IC organic integrated circuit
- O-FET organic field effect transistor
- OF-TFT organic one Thin film transistor
- OF-LET organic light emitting transistor
- O-SC organic solar cell
- O-SC organic optical detector
- O-FQD organic field quench device
- LEC light-emitting electrochemical cell
- O-laser organic laser diode
- inventive functional compound is present as a layer (or in a layer) in the electronic device.
- the present invention thus also provides a layer, in particular an organic layer, containing one or more compounds as defined above.
- the device comprises a plurality of layers.
- the compound according to the invention can preferably be used in a hole transport, hole injection,
- Electron transport, electron injection and / or emission layer may be included. Particularly preferred is the use of
- the present invention accordingly also relates to an electronic device which comprises at least three, but in a preferred embodiment, all of the layers of hole injection, hole transport, emission, electron transport, electron injection,
- the thickness of the layers may preferably be in the range from 1 to 500 nm, particularly preferably in the range from 2 to 200 nm.
- the device may further include layers composed of other low molecular weight compounds or polymers. These can also be generated by evaporation of low molecular weight compounds in a high vacuum.
- the compounds to be used according to the invention may also be preferred to use not as a pure substance but as a mixture (blend) together with further any desired polymeric, oligomeric, dendritic or low molecular weight substances. These can for example improve the electronic properties or emit themselves. Such mixtures are therefore also the subject of the present application.
- the compounds of the invention are used as host materials or
- the organic electroluminescent device may contain one or more emitting layers, wherein at least one emitting layer contains at least one compound according to the invention as defined above. If several emission layers are present, they preferably have a plurality of emission maxima between 380 nm and 750 nm, so that overall white emission results, ie in the emitting Layers use different emitting compounds that can fluoresce or phosphoresce. Very particular preference is given to three-layer systems, the three layers exhibiting blue, green and orange or red emission (for the basic structure see, for example, US Pat
- White emitting devices are useful e.g. as a backlight of LCD displays or for general purpose
- the organic electroluminescent device may also contain further layers, for example one or more hole injection layers, hole transport layers, hole blocking layers, electron transport layers, electron injection layers,
- interlayer can be inserted between two emitting layers.
- Light extraction can be the last organic layer on the
- JQ light exit side in OLEDs for example as nanofoam
- an organic electroluminescent device wherein one or more layers are coated by a sublimation method.
- the materials are stored in vacuum Sublimation plants at a pressure less than 10 "5 mbar, preferably less than 10 " 6 mbar, more preferably less than 10 "7 mbar vapor-deposited.
- an organic electroluminescent device which is characterized in that one or more layers are coated with the OVPD (Organic Vapor Phase Deposition) method or with the aid of a carrier gas sublimation.
- the materials are applied at a pressure between 10 "5 mbar and 1 bar.
- an organic electroluminescent device characterized in that one or more layers of solution, e.g. by spin coating, or by any printing method, e.g. Screen printing, flexographic printing or offset printing, but more preferably LITI (Light Induced Thermal Imaging, thermal transfer printing) or ink-jet printing (ink jet printing) can be produced.
- any printing method e.g. Screen printing, flexographic printing or offset printing, but more preferably LITI (Light Induced Thermal Imaging, thermal transfer printing) or ink-jet printing (ink jet printing) can be produced.
- LITI Light Induced Thermal Imaging, thermal transfer printing
- ink-jet printing ink jet printing
- the device usually includes a cathode and an anode
- the electrodes are selected so that their band energies match those of the adjacent, organic layers as well as possible in order to ensure the most efficient electron or hole injection possible.
- cathode metal complexes low work function metals, metal alloys or multilayer structures of various metals are preferred, such as alkaline earth metals, alkali metals,
- Main group metals or lathanoids eg Ca, Ba, Mg, Al, In, Mg, Yb, Sm, etc.
- other metals which have a relatively high work function such as Ag
- combinations of the metals, for example Ca / Ag or Ba / Ag are generally used.
- alkali metal or alkaline earth metal fluorides for this purpose, for example, alkali metal or alkaline earth metal fluorides, but also the corresponding oxides in question (eg LiF, Ü 2 O, BaF 2 , MgO, NaF, etc.).
- the layer thickness of this layer is preferably between 1 and 10 nm, more preferably between 2 and 8 nm.
- the anode high workfunction materials are preferred.
- the anode has a potential greater than 4.5 eV. Vacuum up.
- metals with a high redox potential such as Ag, Pt or Au, are suitable for this purpose.
- metal / metal oxide electrodes for example Al / Ni / NiO x , Al / PtO x ).
- At least one of the electrodes must be transparent to allow either the irradiation of the organic material (O-SC) or the extraction of light (OLED / PLED, O-LASER).
- O-SC organic material
- O-LASER extraction of light
- a preferred construction uses a transparent anode.
- Preferred anode materials here are conductive, mixed metal oxides. Particularly preferred are indium tin oxide (ITO) or indium zinc oxide (IZO).
- conductive, doped organic materials in particular conductive doped polymers, such as poly (ethylenedioxythiophene) (PEDOT) and polyaniline (PANI).
- PEDOT poly (ethylenedioxythiophene)
- PANI polyaniline
- a method for producing an electronic device in which a formulation of the invention is applied to a substrate and dried, is also an object of the present invention.
- the solvent may be removed at a temperature in the range of -50 ° C to 300 ° C, more preferably in the range of 20 ° C to 250 ° C.
- the drying at a pressure in the range of 10 "3 mbar to 1 bar, more preferably in the range of 10 " 2 mbar to 100 mbar done.
- the device is structured, contacted and finally hermetically sealed in a manner known per se, since the service life of such devices is drastically shortened in the presence of water and / or air.
- the reaction mixture is subsequently stirred at 80 ° C. for 48 hours under a protective gas atmosphere
- the cooled solution is topped up with toluene and washed several times with water, dried and concentrated by evaporation
- the residue is recrystallized from heptane / toluene
- the yield is 21.8 g (26.6 mmol), corresponding to 63.2% of theory.
- the compound 12 is prepared as described in WO 2008/086851 A1.
- the compound 13 is prepared as described in WO 2009/124627.
- the synthesis is analogous to the synthesis of compound 14.
- the yield is 1.5 g (0.95 mmol), corresponding to 55.6% of theory.
- the synthesis is analogous to the synthesis of compound 14.
- the yield is 6.52 g (3.8 mmol), corresponding to 65.6% of theory.
- Tripotassium phosphate are dissolved in 500 ml of toluene, 600 ml of water and 100 ml
- the compound 23 is prepared as described in WO 2009/100925.
- connection 33 is prepared as described in WO 2008/006449.
- PLEDs polymeric light-emitting diodes
- Chlorobenzene dissolved is 20% by weight of the emitter (compounds 14, 15, 16, 19 and 20) and 80% by weight of the matrix materials (compounds 5 to 13, 17 and 18).
- the typical solids content of such solutions is between 16 and 25 g / l, if, as here, the typical for a device layer thickness of 80 nm is to be achieved by spin coating.
- Fig. 1 shows the typical structure of such a device.
- the jointly dissolved matrix materials and the emitter are in the form of an amorphous layer.
- Structured ITO substrates and the material for the so-called buffer layer PEDOT, actually PEDOT: PSS
- PEDOT PPS as aqueous dispersion Clevios P from HC Starck
- the interlayer used HIL-012 from Merck
- the emission layer is in one Inertgasatmospotrore, in the present case argon, spin-coated and baked at 160 ° C or 180 ° C for 10 minutes.
- a cathode of barium and aluminum is evaporated in vacuo.
- the layers HBL and ETL used in the aforementioned examples can also be applied by vapor deposition, and the interlayer can also be replaced by one or more layers which merely have to fulfill the condition by the downstream processing step of the EML deposition from solution not to be replaced again.
- compositions according to the prior art.
- the materials to be used according to the invention are dissolved in toluene or chlorobenzene as described above.
- concentration used in the examples given here is 5% by weight of the emitter (Vdg. 33) and 95% by weight of the matrix materials.
- the typical solids content of such solutions is between 10 and 15 g / l, if, as here, the typical for a device layer thickness of 50 nm means
- the devices are characterized by default, the mentioned OLED examples are not yet optimized.
- Table 2 summarizes the data obtained.
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Abstract
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US13/695,703 US9159930B2 (en) | 2010-11-26 | 2010-11-26 | Formulations and electronic devices |
KR1020177025255A KR101886595B1 (ko) | 2010-05-03 | 2010-11-26 | 제형물 및 전자 소자 |
KR1020127031417A KR101778825B1 (ko) | 2010-05-03 | 2010-11-26 | 제형물 및 전자 소자 |
JP2013508376A JP5837051B2 (ja) | 2010-05-03 | 2010-11-26 | 配合物および電子デバイス |
EP10788016.3A EP2566875B1 (de) | 2010-05-03 | 2010-11-26 | Formulierungen und elektronische vorrichtungen |
CN201080066572.XA CN102869672B (zh) | 2010-05-03 | 2010-11-26 | 制剂和电子器件 |
US14/837,724 US9882135B2 (en) | 2010-05-03 | 2015-08-27 | Formulations and electronic devices |
US15/846,480 US10490747B2 (en) | 2010-05-03 | 2017-12-19 | Formulations and electronic devices |
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PCT/EP2010/002683 WO2010136109A1 (de) | 2009-05-29 | 2010-05-03 | Materialien für organische elektrolumineszenzvorrichtungen |
EPPCT/EP2010/005056 | 2010-08-18 | ||
PCT/EP2010/005056 WO2011032626A1 (de) | 2009-09-16 | 2010-08-18 | Metallkomplexe |
PCT/EP2010/005648 WO2011032686A1 (de) | 2009-09-16 | 2010-09-15 | Formulierungen zur herstellung von elektronischen vorrichtungen |
EPPCT/EP2010/005648 | 2010-09-15 |
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US10490747B2 (en) | 2019-11-26 |
US20180114912A1 (en) | 2018-04-26 |
KR101778825B1 (ko) | 2017-09-14 |
CN105949177A (zh) | 2016-09-21 |
CN105949177B (zh) | 2019-02-01 |
KR20130099814A (ko) | 2013-09-06 |
US20190207114A9 (en) | 2019-07-04 |
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