JPWO2007145136A1 - 発光素子材料および発光素子 - Google Patents
発光素子材料および発光素子 Download PDFInfo
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- JPWO2007145136A1 JPWO2007145136A1 JP2007546358A JP2007546358A JPWO2007145136A1 JP WO2007145136 A1 JPWO2007145136 A1 JP WO2007145136A1 JP 2007546358 A JP2007546358 A JP 2007546358A JP 2007546358 A JP2007546358 A JP 2007546358A JP WO2007145136 A1 JPWO2007145136 A1 JP WO2007145136A1
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- light emitting
- emitting device
- aryl
- light
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- 239000000463 material Substances 0.000 title claims abstract description 128
- -1 pyrene compound Chemical class 0.000 claims abstract description 42
- BBEAQIROQSPTKN-UHFFFAOYSA-N antipyrene Natural products C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims abstract description 27
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims abstract description 25
- 150000001875 compounds Chemical class 0.000 claims description 66
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 56
- 239000010410 layer Substances 0.000 claims description 46
- 229910052757 nitrogen Inorganic materials 0.000 claims description 38
- 125000003118 aryl group Chemical group 0.000 claims description 31
- 125000001424 substituent group Chemical group 0.000 claims description 29
- 125000001072 heteroaryl group Chemical group 0.000 claims description 28
- 239000012044 organic layer Substances 0.000 claims description 24
- 239000002019 doping agent Substances 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 15
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 11
- 125000000304 alkynyl group Chemical group 0.000 claims description 11
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 11
- 125000000623 heterocyclic group Chemical group 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 11
- 125000003277 amino group Chemical group 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 125000004414 alkyl thio group Chemical group 0.000 claims description 9
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 9
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000005013 aryl ether group Chemical group 0.000 claims description 7
- 150000004832 aryl thioethers Chemical group 0.000 claims description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 7
- 125000004434 sulfur atom Chemical group 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- 150000008378 aryl ethers Chemical class 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 abstract description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 60
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 39
- 238000000746 purification Methods 0.000 description 36
- 238000000859 sublimation Methods 0.000 description 36
- 230000008022 sublimation Effects 0.000 description 36
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- 239000000243 solution Substances 0.000 description 32
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- 238000000034 method Methods 0.000 description 29
- 230000032258 transport Effects 0.000 description 27
- 239000013078 crystal Substances 0.000 description 26
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 26
- 238000005160 1H NMR spectroscopy Methods 0.000 description 25
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 24
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 22
- 239000011259 mixed solution Substances 0.000 description 22
- 239000007787 solid Substances 0.000 description 22
- 239000000758 substrate Substances 0.000 description 22
- 230000005525 hole transport Effects 0.000 description 15
- 239000000843 powder Substances 0.000 description 15
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 14
- 238000003786 synthesis reaction Methods 0.000 description 14
- 239000011521 glass Substances 0.000 description 13
- 238000004128 high performance liquid chromatography Methods 0.000 description 13
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 13
- 235000019798 tripotassium phosphate Nutrition 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 12
- 238000009792 diffusion process Methods 0.000 description 12
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 12
- 235000019341 magnesium sulphate Nutrition 0.000 description 12
- 238000005259 measurement Methods 0.000 description 12
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 8
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- 239000010409 thin film Substances 0.000 description 8
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 7
- 101150003085 Pdcl gene Proteins 0.000 description 7
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 7
- 239000012141 concentrate Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 238000010894 electron beam technology Methods 0.000 description 6
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- 239000007924 injection Substances 0.000 description 6
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 6
- 150000003220 pyrenes Chemical class 0.000 description 6
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 6
- 238000007740 vapor deposition Methods 0.000 description 6
- BIWQNIMLAISTBV-UHFFFAOYSA-N (4-methylphenyl)boronic acid Chemical compound CC1=CC=C(B(O)O)C=C1 BIWQNIMLAISTBV-UHFFFAOYSA-N 0.000 description 5
- HYGLETVERPVXOS-UHFFFAOYSA-N 1-bromopyrene Chemical compound C1=C2C(Br)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 HYGLETVERPVXOS-UHFFFAOYSA-N 0.000 description 5
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- PKRRNTJIHGOMRC-UHFFFAOYSA-N 1-benzofuran-2-ylboronic acid Chemical compound C1=CC=C2OC(B(O)O)=CC2=C1 PKRRNTJIHGOMRC-UHFFFAOYSA-N 0.000 description 4
- MQNDWBDMDCOJJJ-UHFFFAOYSA-N 1-bromo-6-(4-methylphenyl)pyrene Chemical compound C1=CC(C)=CC=C1C1=CC=C(C=C2)C3=C4C2=C(Br)C=CC4=CC=C13 MQNDWBDMDCOJJJ-UHFFFAOYSA-N 0.000 description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-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
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
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- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 4
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- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 4
- BUPCSORIGUDIPX-UHFFFAOYSA-N (2-chloro-4-fluorophenyl) hydrogen carbonate Chemical compound OC(=O)OC1=CC=C(F)C=C1Cl BUPCSORIGUDIPX-UHFFFAOYSA-N 0.000 description 3
- NGQSLSMAEVWNPU-YTEMWHBBSA-N 1,2-bis[(e)-2-phenylethenyl]benzene Chemical class C=1C=CC=CC=1/C=C/C1=CC=CC=C1\C=C\C1=CC=CC=C1 NGQSLSMAEVWNPU-YTEMWHBBSA-N 0.000 description 3
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- ZJHMRPBTRSQNPI-UHFFFAOYSA-N benzo[b][1]benzosilole Chemical compound C1=CC=C2[Si]C3=CC=CC=C3C2=C1 ZJHMRPBTRSQNPI-UHFFFAOYSA-N 0.000 description 1
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical class C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- UAPACYXDMGNRMA-UHFFFAOYSA-N c1c(-c(ccc2ccc3c(-c4cc5ccccc5[o]4)c4)c(cc5)c2c3c5c4-c2ccccc2)[o]c2ccccc12 Chemical compound c1c(-c(ccc2ccc3c(-c4cc5ccccc5[o]4)c4)c(cc5)c2c3c5c4-c2ccccc2)[o]c2ccccc12 UAPACYXDMGNRMA-UHFFFAOYSA-N 0.000 description 1
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- 238000010549 co-Evaporation Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
- 150000003950 cyclic amides Chemical class 0.000 description 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical class C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000007946 flavonol Chemical class 0.000 description 1
- HVQAJTFOCKOKIN-UHFFFAOYSA-N flavonol Natural products O1C2=CC=CC=C2C(=O)C(O)=C1C1=CC=CC=C1 HVQAJTFOCKOKIN-UHFFFAOYSA-N 0.000 description 1
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- 125000003983 fluorenyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
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- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
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- 150000002469 indenes Chemical class 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
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- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910000833 kovar Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- BXFYXYKLIORMBI-UHFFFAOYSA-N n,n-diphenyl-4-[2-(2-phenylphenyl)ethenyl]aniline Chemical group C=1C=C(N(C=2C=CC=CC=2)C=2C=CC=CC=2)C=CC=1C=CC1=CC=CC=C1C1=CC=CC=C1 BXFYXYKLIORMBI-UHFFFAOYSA-N 0.000 description 1
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical group C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KPTRDYONBVUWPD-UHFFFAOYSA-N naphthalen-2-ylboronic acid Chemical compound C1=CC=CC2=CC(B(O)O)=CC=C21 KPTRDYONBVUWPD-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 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 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical class [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
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- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 1
- 229920000548 poly(silane) polymer Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 150000004033 porphyrin derivatives Chemical class 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 150000003216 pyrazines Chemical class 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- JOZPEVMCAKXSEY-UHFFFAOYSA-N pyrimido[5,4-d]pyrimidine Chemical group N1=CN=CC2=NC=NC=C21 JOZPEVMCAKXSEY-UHFFFAOYSA-N 0.000 description 1
- RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical class C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 description 1
- 150000005255 pyrrolopyridines Chemical class 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 150000004322 quinolinols Chemical class 0.000 description 1
- 150000004059 quinone derivatives Chemical class 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound 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 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000012916 structural analysis Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000011593 sulfur Substances 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
- 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
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- NZFNXWQNBYZDAQ-UHFFFAOYSA-N thioridazine hydrochloride Chemical class Cl.C12=CC(SC)=CC=C2SC2=CC=CC=C2N1CCC1CCCCN1C NZFNXWQNBYZDAQ-UHFFFAOYSA-N 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- PWYVVBKROXXHEB-UHFFFAOYSA-M trimethyl-[3-(1-methyl-2,3,4,5-tetraphenylsilol-1-yl)propyl]azanium;iodide Chemical compound [I-].C[N+](C)(C)CCC[Si]1(C)C(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 PWYVVBKROXXHEB-UHFFFAOYSA-M 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000001651 triphenylamine derivatives Chemical class 0.000 description 1
- 125000005580 triphenylene group Chemical group 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000001039 wet etching Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
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- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron compounds
- C07F5/027—Organoboranes and organoborohydrides
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- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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- 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
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- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/322—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising boron
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- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
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- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
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- H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
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- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
Abstract
Description
化合物[1]の合成
1−ブロモピレン1gをジエチルエーテル40mlに溶解し、窒素雰囲気下、0℃でn−ブチルリチウム(1.6M ヘキサン溶液)2.3mlを滴下した。混合溶液を室温で10分撹拌した後、ジメシチルボロンフルオライド965mgをジエチルエーテル12mlに溶解したものを滴下し、さらに10分間加熱還流した。溶液を室温に冷却した後、ろ過した。得られた固体を酢酸エチルから再結晶し、シリカゲルクロマトグラフィーにより精製し、真空乾燥した後、淡黄色結晶0.52gを得た。得られた粉末の1H−NMR分析結果は次の通りであり、上記で得られた淡黄色結晶が化合物〔1〕であることが確認された。
1H−NMR(CDCl3(d=ppm)):1.95(s, 12H), 2.32(s, 6H) , 6.81(s, 4H) , 7.85-8.19(m, 9H)。
化合物[14]の合成
1,6−ジブロモピレン2g、4−メチルフェニルボロン酸1g、リン酸三カリウム2.4g、テトラブチルアンモニウムブロミド0.4g、酢酸パラジウム22mgおよびジメチルホルムアミド60mlの混合溶液を窒素気流下、130℃で6時間加熱撹拌した。溶液を室温に冷却した後、水30mlを注入し、ジクロロメタン100mlで抽出した。有機層を水50mlで2回洗浄し、硫酸マグネシウムで乾燥後、エバポレートした。得られた濃縮物をシリカゲルカラムクロマトグラフィーにより精製し、真空乾燥した後、1−ブロモ−6−(4−メチルフェニル)ピレン0.7gを得た。
1H−NMR(CDCl3(d=ppm)):1.96(s, 12H), 2.33(s, 6H) , 2.50(s, 3H) , 6.82(s, 4H) , 7.36-7.53(m, 4H) , 7.86-8.25(m, 8H)。
化合物[13]の合成
4−メチルフェニルボロン酸の代わりにフェニルボロン酸を用いた以外は実施例2と同様の方法で合成し、淡黄色結晶0.47gを得た。得られた粉末の1H−NMR分析結果は次の通りであり、上記で得られた淡黄色結晶が化合物[13]であることが確認された。
1H−NMR(CDCl3(d=ppm)):1.96(s, 12H), 2.33(s, 6H) , 6.82(s, 4H) , 7.45-7.63(m, 5H) , 7.87-8.22(m, 8H)。
化合物[19]の合成
1−ブロモピレン7.0g、2−ナフタレンボロン酸4.7g、リン酸三カリウム11.6g、テトラブチルアンモニウムブロミド1.8g、酢酸パラジウム0.11gおよびジメチルホルムアミド248mlの混合溶液を窒素気流下、130℃で5時間加熱撹拌した。溶液を室温に冷却した後、水300mlを注入し、室温で0.5h撹拌した。析出した固体をろ取し、水100mlで2回洗浄した。得られた固体をジクロロメタン200mlに溶解し、硫酸マグネシウムで乾燥後、セライトを用いてろ過した。ろ液をエバポレートし、残さをメタノール100mlで2回洗浄し、析出した固体をろ取した。真空乾燥した後、1−(2−ナフチル)ピレン7.5gを得た。
1H−NMR(CDCl3(d=ppm)):1.96(s, 12H), 2.33(s, 6H) , 6.82(s, 4H) , 7.54-7.60(m, 2H) , 7.74-7.78(m, 1H) , 7.89-8.26(m, 12H)。
化合物[61]の合成
1−ブロモピレン1.1g、2−ベンゾフランボロン酸0.8g、リン酸三カリウム2.1g、PdCl2(dppf)・CH2Cl298mgと脱気したジメチルホルムアミド15mlとの混合溶液を窒素気流下、130℃で3時間加熱撹拌した。溶液を室温に冷却した後、水30mlを注入し、ジクロロメタン50mlで抽出した。有機層を水50mlで2回洗浄し、硫酸マグネシウムで乾燥後、エバポレートした。得られた濃縮物をシリカゲルカラムクロマトグラフィーにより精製し、真空乾燥した後、黄色結晶0.34gを得た。得られた粉末の1H−NMR分析結果は次の通りであり、上記で得られた黄色結晶が化合物[61]であることが確認された。
1H−NMR(CDCl3(d=ppm)):7.25-7.41(m, 3H), 7.65-7.74(m, 2H), 8.02-8.27(m, 7H), 8.40-8.43(m, 1H), 8.80(d, 1H)。
化合物[156]の合成
1,6−ジブロモピレン0.72g、2−ベンゾフランボロン酸0.8g、リン酸三カリウム2.1g、PdCl2(dppf)・CH2Cl298mgと脱気したジメチルホルムアミド15mlとの混合溶液を窒素気流下、130℃で4時間加熱撹拌した。溶液を室温に冷却した後、水30mlを注入し、ろ過した。得られた固体をエタノール30mlで洗浄した後、ジメチルホルムアミドから再結晶し、真空乾燥した後、黄色結晶0.51gを得た。得られた粉末の1H−NMR分析結果は次の通りであり、上記で得られた黄色結晶が化合物[156]であることが確認された。
1H−NMR(CDCl3(d=ppm)):7.26-7.42(m, 6H), 7.66-7.75(m, 4H), 8.18-8.30(m, 4H), 8.42-8.45(m, 2H), 8.84(d, 2H)。
化合物[79]の合成
1,6−ジブロモピレン2g、4−メチルフェニルボロン酸1.9g、リン酸三カリウム5.9g、テトラブチルアンモニウムブロミド0.9g、酢酸パラジウム15mgおよびジメチルホルムアミド30mlの混合溶液を窒素気流下、130℃で6時間加熱撹拌した。溶液を室温に冷却した後、水30mlを注入し、ろ過した。得られた固体をエタノール30mlで洗浄した後、トルエンから再結晶し、真空乾燥した後、1,6−ビス(4−メチルフェニル)ピレン1.3gを得た。
1H−NMR(CDCl3(d=ppm)):2.51(ss, 6H), 7.24-7.42(m, 7H), 7.55-7.70(m, 6H), 7.99-8.40(m, 6H), 8.74(d, 1H)。
化合物[87]の合成
1,6−ジブロモピレン2g、4−フルオロフェニルボロン酸2.3g、リン酸三カリウム7.0g、テトラブチルアンモニウムブロミド1.1g、酢酸パラジウム74mgおよびジメチルホルムアミド50mlの混合溶液を窒素気流下、130℃で6時間加熱撹拌した。溶液を室温に冷却した後、水50mlを注入し、ジクロロメタン100mlで抽出した。有機層を水50mlで2回洗浄し、硫酸マグネシウムで乾燥後、エバポレートした。得られた固体をメタノール30mlで洗浄し、真空乾燥した後、1,6−ビス(4−フルオロフェニル)ピレン1.8gを得た。
1H−NMR(CDCl3(d=ppm)):7.24-7.39(m, 7H), 7.58-7.71(m, 6H), 7.98-8.38(m, 6H), 8.77(d, 1H)。
化合物[97]の合成
1−ブロモピレン5g、N−ブロモスクシンイミド7.9gおよびジメチルホルムアミド140mlの混合溶液を窒素気流下、80℃で10時間撹拌した。溶液を室温に冷却した後、水400mlを注入し、析出物をろ過した。ろ別した固体を水50ml、メタノール100mlおよびジクロロメタン200mlでそれぞれ洗浄した後、真空乾燥して、1,3,6−トリブロモピレン6.1gを淡黄土色粉末として得た。
1H−NMR(CDCl3(d=ppm)):2.48-2.50(m, 9H), 7.26-7.71(m, 17H), 8.01-8.40(m, 5H), 8.75(d, 1H)。
化合物[137]の合成
1−ブロモピレン45.0g、4−メチルフェニルボロン酸21.7g、リン酸三カリウム34.0g、テトラブチルアンモニウムブロミド10.3g、酢酸パラジウム0.71gおよびジメチルホルムアミド1.6Lの混合溶液を窒素気流下、120℃で5時間加熱撹拌した。溶液を室温に冷却した後、水1.6Lを注入し、室温で0.5h撹拌した。析出した固体をろ取し、水200mlで2回洗浄した。得られた固体をジクロロメタン500mlに溶解し、硫酸マグネシウムで乾燥後、セライトを用いてろ過した。ろ液をエバポレートし、残さをメタノール200mlで2回洗浄し、析出した固体をろ取し、真空乾燥して、1−(4−メチルフェニル)ピレン40.0gを得た。
1H−NMR(CDCl3(d=ppm)):1.44(s, 9H), 2.52(s, 3H), 7.25-7.71(18m, H), 8.27-8.33(m, 2H), 8.43-8.45(m, 2H), 8.79(d, 2H)。
化合物[134]の合成
2−(3−t−ブチルフェニル)−4,4,5,5−テトラメチル1,3,2−ジオキサボロランの代わりに3−メチルフェニルボロン酸を用いた以外は実施例10と同様の方法で合成し、黄色結晶を得た。得られた粉末の1H−NMR分析結果は次の通りであり、上記で得られた黄色結晶が化合物[134]であることが確認された。
1H−NMR(CDCl3(d=ppm)):2.52(ss, 6H), 7.27-7.71(18m, H), 8.28-8.33(m, 2H), 8.44(ss, 2H), 8.80(d, 2H)。
化合物[136]の合成
2−(3−t−ブチルフェニル)−4,4,5,5−テトラメチル1,3,2−ジオキサボロランの代わりに4−t−ブチルフェニルボロン酸を用いた以外は実施例10と同様の方法で合成し、黄色結晶を得た。得られた粉末の1H−NMR分析結果は次の通りであり、上記で得られた黄色結晶が化合物[136]であることが確認された。
1H−NMR(CDCl3(d=ppm)):1.46(s, 9H), 2.52(s, 3H), 7.26-7.71(18m, H), 8.28-8.36(m, 2H), 8.43-8.46(m, 2H), 8.77-8.82(m, 2H)。
化合物[14]を用いた発光素子を次のように作製した。30×40mmのガラス基板(旭硝子(株)製、15Ω/□、電子ビーム蒸着品)上にITO導電膜をガラス基板中央部分に150nmの厚さで30×13mmの大きさに形成し、陽極とした。陽極が形成された基板を“セミコクリン(登録商標)56”(フルウチ化学(株)製)で15分間超音波洗浄してから、超純水で洗浄した。続いて、この基板をイソプロピルアルコールで15分間超音波洗浄してから、熱メタノールに15分間浸漬させた後、乾燥させた。素子を作製する直前にこの基板を1時間UV−オゾン処理し、さらに真空蒸着装置内に設置して、装置内の真空度が5×10−5Pa以下になるまで排気した。
ドーパント材料として表1〜2に記載した材料を用いた以外は、実施例13と同様にして発光素子を作製した。各実施例の結果は表1〜2に示した。
ホスト材料として表3に記載した材料を用いた以外は、実施例13と同様にして発光素子を作製した。各実施例の結果は表3に示した。
電子輸送材料として表4に記載した材料を用いた以外は、実施例13と同様にして発光素子を作製した。各実施例の結果は表4に示した。
ドーパント材料として化合物[137]をドープ濃度が2%となるように用いた以外は、実施例13と同様にして発光素子を作製した。この発光素子を10mA/cm2で直流駆動したところ、発光効率5.2lm/Wの高効率発光と、C.I.E色度座標で(0.34,0.66)と高色純度の緑色発光が得られた。
ドーパント材料として化合物[134]をドープ濃度が2%となるように用いた以外は、実施例13と同様にして発光素子を作製した。この発光素子を10mA/cm2で直流駆動したところ、発光効率5.8lm/Wの高効率発光と、C.I.E色度座標で(0.35,0.65)と高色純度の緑色発光が得られた。
ドーパント材料として化合物[136]をドープ濃度が2%となるように用いた以外は、実施例13と同様にして発光素子を作製した。この発光素子を10mA/cm2で直流駆動したところ、発光効率6.0lm/Wの高効率発光と、C.I.E色度座標で(0.34,0.66)と高色純度の緑色発光が得られた。
発光材料として、ホスト材料としてH−1を、ドーパント材料としてD−3をドープ濃度が5%になるように5nmの厚さに蒸着したのち、さらに発光材料として、ホスト材料としてH−1を、ドーパント材料として化合物[14]をドープ濃度が2%になるように30nmの厚さに積層した以外は、実施例13と同様にして発光素子を作製した。この発光素子を10mA/cm2で直流駆動したところ、発光効率6.2lm/Wの高効率白色発光が得られた。この発光素子を10mA/cm2の直流で連続駆動したところ、輝度半減時間は10000時間であった。
30×40mmのガラス基板(旭硝子(株)製、15Ω/□、電子ビーム蒸着品)上にITO導電膜をガラス基板中央部分に150nmの厚さで30×13mmの大きさに形成し、陽極とした。陽極が形成された基板をアセトンおよび“セミコクリン(登録商標)56”(フルウチ化学(株)製)で各々15分間超音波洗浄してから、超純水で洗浄した。続いて、基板をイソプロピルアルコールで15分間超音波洗浄してから、熱メタノールに15分間浸漬させた後、乾燥させた。この基板を素子を作製する直前に1時間UV−オゾン処理し、さらに真空蒸着装置内に設置して、装置内の真空度が5×10−4Pa以下になるまで排気した。
Claims (11)
- 一般式(1)で表されるピレン化合物を含有する発光素子材料;
- R1、R3、R6およびR8のうちいずれか1つが一般式(2)で表される置換基である請求項1記載の発光素子材料。
- R12、R14およびR16がメチル基である請求項1または2記載の発光素子材料。
- R1、R3、R6およびR8のうち少なくとも1つが一般式(3)で表される置換基である請求項1記載の発光素子材料。
- Xが酸素原子である請求項4記載の発光素子材料。
- R1〜R10の少なくとも1つがアルキル基またはアリール基である請求項1〜5のいずれかに記載の発光素子材料。
- R1が一般式(2)または(3)で表される置換基であり、かつ、R6もしくはR8がアリール基またはヘテロアリール基である請求項1記載の発光素子材料。
- R3およびR8がアリール基またはヘテロアリール基である請求項7記載の発光素子材料。
- 陽極、陰極および該陽極と該陰極の間に存在する有機層を有し、該有機層は少なくとも発光層を含み、該発光層が電気エネルギーにより発光する発光素子であって、該有機層が請求項1に記載の発光素子材料を含有する発光素子。
- 発光層がホスト材料とドーパント材料を含み、かつ、ドーパント材料が一般式(1)で表されるピレン化合物である請求項9に記載の発光素子。
- 発光層と陰極の間にさらに電子輸送層が存在し、該電子輸送層が、電子受容性窒素を含み、さらに炭素、水素、窒素、酸素、ケイ素およびリンの中から選ばれる元素で構成されるヘテロアリール環構造を有する化合物を含有する請求項9または10に記載の発光素子。
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- 2007-06-08 KR KR1020087024201A patent/KR101378047B1/ko not_active IP Right Cessation
- 2007-06-08 EP EP07767065.1A patent/EP2028249B1/en not_active Not-in-force
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US11793063B2 (en) * | 2014-12-24 | 2023-10-17 | Samsung Display Co., Ltd. | Condensed-cyclic compound and organic light emitting device including the same |
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TW200811268A (en) | 2008-03-01 |
US20100163852A1 (en) | 2010-07-01 |
US8729530B2 (en) | 2014-05-20 |
TWI444455B (zh) | 2014-07-11 |
EP2028249A1 (en) | 2009-02-25 |
CN101473012A (zh) | 2009-07-01 |
KR20090017475A (ko) | 2009-02-18 |
WO2007145136A1 (ja) | 2007-12-21 |
CN101473012B (zh) | 2013-12-18 |
JP5326280B2 (ja) | 2013-10-30 |
EP2028249B1 (en) | 2013-05-08 |
KR101378047B1 (ko) | 2014-03-27 |
EP2028249A4 (en) | 2010-07-21 |
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