JP2004536134A - 複素環基を含む第３級ジアミン及び有機電子冷光放射装置におけるその使用 - Google Patents
複素環基を含む第３級ジアミン及び有機電子冷光放射装置におけるその使用 Download PDFInfo
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- JP2004536134A JP2004536134A JP2003514065A JP2003514065A JP2004536134A JP 2004536134 A JP2004536134 A JP 2004536134A JP 2003514065 A JP2003514065 A JP 2003514065A JP 2003514065 A JP2003514065 A JP 2003514065A JP 2004536134 A JP2004536134 A JP 2004536134A
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- Prior art keywords
- halogen
- alkyl
- cycloalkyl
- nitro
- optionally substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 125000000623 heterocyclic group Chemical group 0.000 title claims abstract description 12
- 150000004985 diamines Chemical group 0.000 title description 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 63
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 58
- 150000002367 halogens Chemical class 0.000 claims abstract description 56
- 150000001875 compounds Chemical class 0.000 claims abstract description 46
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 46
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 41
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 41
- 125000003118 aryl group Chemical group 0.000 claims abstract description 35
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims abstract description 21
- 125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 10
- 125000005843 halogen group Chemical group 0.000 claims abstract description 10
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 9
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 9
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
- 125000002619 bicyclic group Chemical group 0.000 claims abstract description 6
- 125000004999 nitroaryl group Chemical group 0.000 claims abstract 2
- 239000000463 material Substances 0.000 claims description 15
- 230000005525 hole transport Effects 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 8
- -1 6-quinolyl Chemical group 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 229910052740 iodine Inorganic materials 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000003107 substituted aryl group Chemical group 0.000 claims description 3
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 2
- 125000005493 quinolyl group Chemical group 0.000 claims 1
- 239000010410 layer Substances 0.000 description 32
- 238000002347 injection Methods 0.000 description 26
- 239000007924 injection Substances 0.000 description 26
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
- 229910052757 nitrogen Inorganic materials 0.000 description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 230000005855 radiation Effects 0.000 description 11
- 239000000047 product Substances 0.000 description 10
- 101150097195 TLG1 gene Proteins 0.000 description 9
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 9
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 8
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 6
- 229910052739 hydrogen Inorganic materials 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
- 239000011541 reaction mixture Substances 0.000 description 6
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 229910052794 bromium Inorganic materials 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 150000003512 tertiary amines Chemical group 0.000 description 5
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 4
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 0 *N(*)[Al]N(*)* Chemical compound *N(*)[Al]N(*)* 0.000 description 3
- USSDZGUORVTLQJ-UHFFFAOYSA-N 9-ethyl-3-iodocarbazole Chemical compound IC1=CC=C2N(CC)C3=CC=CC=C3C2=C1 USSDZGUORVTLQJ-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000004020 luminiscence type Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 125000001725 pyrenyl group Chemical group 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 150000003335 secondary amines Chemical class 0.000 description 3
- 238000000859 sublimation Methods 0.000 description 3
- 230000008022 sublimation Effects 0.000 description 3
- OHQKUENDBYRKDI-UHFFFAOYSA-N 9-ethyl-n-[4-[4-(n-(9-ethylcarbazol-3-yl)anilino)phenyl]phenyl]-n-phenylcarbazol-3-amine Chemical compound C=1C=C2N(CC)C3=CC=CC=C3C2=CC=1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=C2C3=CC=CC=C3N(CC)C2=CC=1)C1=CC=CC=C1 OHQKUENDBYRKDI-UHFFFAOYSA-N 0.000 description 2
- WHBVYTHKWHEJJU-UHFFFAOYSA-N 9-ethyl-n-[4-[4-[(9-ethylcarbazol-3-yl)-naphthalen-1-ylamino]phenyl]phenyl]-n-naphthalen-1-ylcarbazol-3-amine Chemical compound C1=CC=C2C(N(C=3C=CC(=CC=3)C=3C=CC(=CC=3)N(C=3C=C4C5=CC=CC=C5N(CC)C4=CC=3)C=3C4=CC=CC=C4C=CC=3)C=3C=C4C5=CC=CC=C5N(C4=CC=3)CC)=CC=CC2=C1 WHBVYTHKWHEJJU-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 2
- UHOVQNZJYSORNB-MZWXYZOWSA-N benzene-d6 Chemical compound [2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1[2H] UHOVQNZJYSORNB-MZWXYZOWSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical compound C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 125000006575 electron-withdrawing group Chemical group 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- RDOWQLZANAYVLL-UHFFFAOYSA-N phenanthridine Chemical compound C1=CC=C2C3=CC=CC=C3C=NC2=C1 RDOWQLZANAYVLL-UHFFFAOYSA-N 0.000 description 2
- 229960005235 piperonyl butoxide Drugs 0.000 description 2
- FDRNXKXKFNHNCA-UHFFFAOYSA-N 4-(4-anilinophenyl)-n-phenylaniline Chemical compound C=1C=C(C=2C=CC(NC=3C=CC=CC=3)=CC=2)C=CC=1NC1=CC=CC=C1 FDRNXKXKFNHNCA-UHFFFAOYSA-N 0.000 description 1
- QVRBGKYLLCLCHL-UHFFFAOYSA-N CC1C=CC=C1 Chemical compound CC1C=CC=C1 QVRBGKYLLCLCHL-UHFFFAOYSA-N 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000001503 aryl iodides Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000005647 linker group Chemical group 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
- SMXKPSLCRALELV-UHFFFAOYSA-N methyl 4-pyridin-3-ylbenzoate Chemical compound C1=CC(C(=O)OC)=CC=C1C1=CC=CN=C1 SMXKPSLCRALELV-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical compound 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
- BWGZFKYCFHATQH-UHFFFAOYSA-N n-[4-[4-(quinolin-6-ylamino)phenyl]phenyl]quinolin-6-amine Chemical compound N1=CC=CC2=CC(NC=3C=CC(=CC=3)C=3C=CC(NC=4C=C5C=CC=NC5=CC=4)=CC=3)=CC=C21 BWGZFKYCFHATQH-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
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 230000001443 photoexcitation Effects 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound 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
- 229920000642 polymer Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 125000001424 substituent group Chemical group 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
- 239000010409 thin film Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000005259 triarylamine group Chemical group 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0117377.2A GB0117377D0 (en) | 2001-07-17 | 2001-07-17 | "Tertiary diamines containing heterocyclic groups and their use in organic electroluminescent devices" |
| PCT/GB2002/003115 WO2003008515A1 (en) | 2001-07-17 | 2002-07-04 | Tertiary diamines containing heterocyclic groups and their use in organic electroluminescent devices |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004536134A true JP2004536134A (ja) | 2004-12-02 |
| JP2004536134A5 JP2004536134A5 (enExample) | 2005-11-17 |
Family
ID=9918637
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003514065A Withdrawn JP2004536134A (ja) | 2001-07-17 | 2002-07-04 | 複素環基を含む第３級ジアミン及び有機電子冷光放射装置におけるその使用 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20040185299A1 (enExample) |
| EP (1) | EP1406983A1 (enExample) |
| JP (1) | JP2004536134A (enExample) |
| GB (1) | GB0117377D0 (enExample) |
| WO (1) | WO2003008515A1 (enExample) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007020804A1 (en) * | 2005-08-12 | 2007-02-22 | Semiconductor Energy Laboratory Co., Ltd. | Arylamine compound and synthetic method thereof |
| JP2007070352A (ja) * | 2005-08-12 | 2007-03-22 | Semiconductor Energy Lab Co Ltd | アリールアミン化合物およびその合成方法、並びにアリールアミン化合物を用いて得られる発光素子用材料、発光素子、電子機器 |
| WO2007043484A1 (ja) * | 2005-10-07 | 2007-04-19 | Toyo Ink Manufacturing Co., Ltd. | カルバゾール含有アミン化合物及びその用途 |
| WO2008001551A1 (en) | 2006-06-27 | 2008-01-03 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescence device using the same |
| JP2009185030A (ja) * | 2008-02-11 | 2009-08-20 | Samsung Mobile Display Co Ltd | 有機発光素子及びそれを備えた平板表示装置 |
| WO2010061824A1 (ja) * | 2008-11-25 | 2010-06-03 | 出光興産株式会社 | 芳香族アミン誘導体及び有機エレクトロルミネッセンス素子 |
| KR101050459B1 (ko) * | 2008-09-03 | 2011-07-20 | 삼성모바일디스플레이주식회사 | 플루오렌 화합물 및 이를 이용한 유기 전계 발광 장치 |
| KR20140134884A (ko) * | 2013-05-15 | 2014-11-25 | 에스에프씨 주식회사 | 유기발광 화합물 및 이를 포함하는 유기전계발광소자 |
| US9142783B2 (en) | 2004-11-30 | 2015-09-22 | Semiconductor Energy Laboratory Co., Ltd. | Light emitting element and light emitting device |
| KR20150144487A (ko) * | 2014-06-17 | 2015-12-28 | 에스에프씨 주식회사 | 방향족 아민기를 포함하는 신규한 아민 화합물 및 이를 포함하는 유기 발광 소자 |
| JP2016065104A (ja) * | 2009-03-31 | 2016-04-28 | 株式会社半導体エネルギー研究所 | キノキサリン誘導体、キノキサリン誘導体を用いた発光素子、発光装置、照明装置及び電子機器 |
| JP2016520253A (ja) * | 2013-04-27 | 2016-07-11 | 広東阿格蕾雅光電材料有限公司 | 有機エレクトロルミネッセンス素子 |
| KR101913462B1 (ko) * | 2008-06-30 | 2018-10-30 | 유니버셜 디스플레이 코포레이션 | 황 함유 그룹을 포함하는 정공 수송 물질 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1836024B (zh) * | 2003-08-19 | 2011-03-16 | 默克专利有限公司 | 含有三苯基膦单元的低聚物和聚合物 |
| WO2005064995A1 (en) * | 2003-12-26 | 2005-07-14 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element |
| KR100787425B1 (ko) | 2004-11-29 | 2007-12-26 | 삼성에스디아이 주식회사 | 페닐카바졸계 화합물 및 이를 이용한 유기 전계 발광 소자 |
| KR100846586B1 (ko) * | 2006-05-29 | 2008-07-16 | 삼성에스디아이 주식회사 | 유기 발광 소자 및 이를 구비한 평판 표시 장치 |
| US8188315B2 (en) | 2004-04-02 | 2012-05-29 | Samsung Mobile Display Co., Ltd. | Organic light emitting device and flat panel display device comprising the same |
| KR101251622B1 (ko) * | 2004-09-24 | 2013-04-08 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광장치 |
| CN100565963C (zh) * | 2004-09-30 | 2009-12-02 | 株式会社半导体能源研究所 | 发光元件 |
| JP5032016B2 (ja) * | 2004-10-19 | 2012-09-26 | 株式会社半導体エネルギー研究所 | カルバゾール誘導体およびカルバゾール誘導体を用いた発光素子、並びに発光装置 |
| WO2006043647A1 (en) | 2004-10-19 | 2006-04-27 | Semiconductor Energy Laboratory Co., Ltd. | Carbazole derivative, and light emitting element and light emitting device using the carbazole derivative |
| US8021765B2 (en) | 2004-11-29 | 2011-09-20 | Samsung Mobile Display Co., Ltd. | Phenylcarbazole-based compound and organic electroluminescent device employing the same |
| KR100846608B1 (ko) | 2007-07-30 | 2008-07-16 | 삼성에스디아이 주식회사 | 유기 발광 소자 및 이를 구비한 평판 표시 장치 |
| JPWO2010098023A1 (ja) * | 2009-02-26 | 2012-08-30 | 出光興産株式会社 | 新規重合性単量体とその重合体、それを用いた有機デバイス用材料、正孔注入輸送材料及び有機エレクトロルミネッセンス素子 |
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| CN107903274A (zh) * | 2017-12-28 | 2018-04-13 | 窦玉玲 | 一种胺类化合物及其在抗肿瘤药物中的应用 |
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| JPH034232A (ja) * | 1989-05-31 | 1991-01-10 | Canon Inc | 電子写真感光体 |
| JP4088985B2 (ja) * | 1997-05-09 | 2008-05-21 | コニカミノルタホールディングス株式会社 | 新規アミノ化合物を使用した有機エレクトロルミネセンス素子 |
| US6517957B1 (en) * | 1997-05-19 | 2003-02-11 | Canon Kabushiki Kaisha | Organic compound and electroluminescent device using the same |
| JPH11329737A (ja) * | 1998-03-13 | 1999-11-30 | Taiho Ind Co Ltd | 有機多層型エレクトロルミネッセンス素子及び有機多層型エレクトロルミネッセンス素子用構造体の合成方法 |
| JP2000007670A (ja) * | 1998-06-16 | 2000-01-11 | Takasago Internatl Corp | 新規ビス（３，４−メチレンジオキシフェニルアミノ）誘導体、及び該誘導体を含有する電子写真感光体 |
| EP1029909A4 (en) * | 1998-09-09 | 2007-01-10 | Idemitsu Kosan Co | ORGANIC ELECTROLUMINESCENT DEVICE AND PHENYLENEDIAMINE DERIVATIVE |
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- 2001-07-17 GB GBGB0117377.2A patent/GB0117377D0/en not_active Ceased
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2002
- 2002-07-04 WO PCT/GB2002/003115 patent/WO2003008515A1/en not_active Ceased
- 2002-07-04 EP EP02743418A patent/EP1406983A1/en not_active Withdrawn
- 2002-07-04 JP JP2003514065A patent/JP2004536134A/ja not_active Withdrawn
- 2002-07-04 US US10/483,802 patent/US20040185299A1/en not_active Abandoned
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| JP2007070352A (ja) * | 2005-08-12 | 2007-03-22 | Semiconductor Energy Lab Co Ltd | アリールアミン化合物およびその合成方法、並びにアリールアミン化合物を用いて得られる発光素子用材料、発光素子、電子機器 |
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| WO2008001551A1 (en) | 2006-06-27 | 2008-01-03 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescence device using the same |
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| WO2010061824A1 (ja) * | 2008-11-25 | 2010-06-03 | 出光興産株式会社 | 芳香族アミン誘導体及び有機エレクトロルミネッセンス素子 |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO2003008515A1 (en) | 2003-01-30 |
| EP1406983A1 (en) | 2004-04-14 |
| GB0117377D0 (en) | 2001-09-05 |
| US20040185299A1 (en) | 2004-09-23 |
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