JP2008539192A5 - - Google Patents
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- Publication number
- JP2008539192A5 JP2008539192A5 JP2008508194A JP2008508194A JP2008539192A5 JP 2008539192 A5 JP2008539192 A5 JP 2008539192A5 JP 2008508194 A JP2008508194 A JP 2008508194A JP 2008508194 A JP2008508194 A JP 2008508194A JP 2008539192 A5 JP2008539192 A5 JP 2008539192A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- aryl
- interrupted
- alkoxy
- 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.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims description 98
- 125000003118 aryl group Chemical group 0.000 claims description 57
- 125000003545 alkoxy group Chemical group 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 14
- 125000001072 heteroaryl group Chemical group 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 13
- 150000002367 halogens Chemical class 0.000 claims description 13
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 11
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 8
- -1 diphenylamino Chemical group 0.000 claims 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 6
- 125000005427 anthranyl group Chemical group 0.000 claims 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 6
- 125000005561 phenanthryl group Chemical group 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- 125000001624 naphthyl group Chemical group 0.000 claims 5
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 4
- 125000002877 alkyl aryl group Chemical group 0.000 claims 4
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 125000001589 carboacyl group Chemical group 0.000 claims 3
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 2
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims 1
- 125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims 1
- OGNSDRMLWYNUED-UHFFFAOYSA-N 1-cyclohexyl-4-[4-[4-(4-cyclohexylcyclohexyl)cyclohexyl]cyclohexyl]cyclohexane Chemical group C1CCCCC1C1CCC(C2CCC(CC2)C2CCC(CC2)C2CCC(CC2)C2CCCCC2)CC1 OGNSDRMLWYNUED-UHFFFAOYSA-N 0.000 claims 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000004054 acenaphthylenyl group Chemical group C1(=CC2=CC=CC3=CC=CC1=C23)* 0.000 claims 1
- 125000003172 aldehyde group Chemical group 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000004419 alkynylene group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000000732 arylene group Chemical group 0.000 claims 1
- 125000002908 as-indacenyl group Chemical group C1(=CC=C2C=CC3=CC=CC3=C12)* 0.000 claims 1
- 125000003828 azulenyl group Chemical group 0.000 claims 1
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 125000002676 chrysenyl group Chemical group C1(=CC=CC=2C3=CC=C4C=CC=CC4=C3C=CC12)* 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005549 heteroarylene group Chemical group 0.000 claims 1
- 125000001633 hexacenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC5=CC6=CC=CC=C6C=C5C=C4C=C3C=C12)* 0.000 claims 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims 1
- 125000000468 ketone group Chemical group 0.000 claims 1
- 125000004957 naphthylene group Chemical group 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000003933 pentacenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C12)* 0.000 claims 1
- JQQSUOJIMKJQHS-UHFFFAOYSA-N pentaphenyl group Chemical group C1=CC=CC2=CC3=CC=C4C=C5C=CC=CC5=CC4=C3C=C12 JQQSUOJIMKJQHS-UHFFFAOYSA-N 0.000 claims 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims 1
- 108091008695 photoreceptors Proteins 0.000 claims 1
- 125000001388 picenyl group Chemical group C1(=CC=CC2=CC=C3C4=CC=C5C=CC=CC5=C4C=CC3=C21)* 0.000 claims 1
- 125000003367 polycyclic group Chemical group 0.000 claims 1
- 125000001725 pyrenyl group Chemical group 0.000 claims 1
- 125000005401 siloxanyl group Chemical group 0.000 claims 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000001935 tetracenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C12)* 0.000 claims 1
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 1
- 125000003960 triphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C3=CC=CC=C3C12)* 0.000 claims 1
- SKXVPBISAIXBHP-UHFFFAOYSA-N C(C1)C(c2nc(-c(cc3)ccc3-c3cc4ccccc4cc3)n[n]2-c2c(cccc3)c3ccc2)=CC=C1c1cc2ccccc2cc1 Chemical compound C(C1)C(c2nc(-c(cc3)ccc3-c3cc4ccccc4cc3)n[n]2-c2c(cccc3)c3ccc2)=CC=C1c1cc2ccccc2cc1 SKXVPBISAIXBHP-UHFFFAOYSA-N 0.000 description 1
- INKRVNOINFRNGR-MHMUNSBRSA-N C(c1ccccc1)=C\c(cc1)ccc1-c1nc(-c2ccc(/C=C\c3ccccc3)cc2)n[n]1-c1ccccc1 Chemical compound C(c1ccccc1)=C\c(cc1)ccc1-c1nc(-c2ccc(/C=C\c3ccccc3)cc2)n[n]1-c1ccccc1 INKRVNOINFRNGR-MHMUNSBRSA-N 0.000 description 1
- IACNLOHVXMOTKV-UHFFFAOYSA-N C1C=C(C=CC(c2cccc(-c3nc(-c(cc4)ccc4-c4ccc(C=CCC5)c5c4)n[n]3-c3ccccc3)c2)=C2)C2=CC1 Chemical compound C1C=C(C=CC(c2cccc(-c3nc(-c(cc4)ccc4-c4ccc(C=CCC5)c5c4)n[n]3-c3ccccc3)c2)=C2)C2=CC1 IACNLOHVXMOTKV-UHFFFAOYSA-N 0.000 description 1
- OOWHQAMRLSZFAY-UHFFFAOYSA-N c(cc1)ccc1-[n]1nc(-c(cc2)ccc2-c2c(ccc3cccc(cc4)c33)c3c4cc2)nc1-c(cc1)ccc1-c1c(ccc2cccc(cc3)c22)c2c3cc1 Chemical compound c(cc1)ccc1-[n]1nc(-c(cc2)ccc2-c2c(ccc3cccc(cc4)c33)c3c4cc2)nc1-c(cc1)ccc1-c1c(ccc2cccc(cc3)c22)c2c3cc1 OOWHQAMRLSZFAY-UHFFFAOYSA-N 0.000 description 1
- BPBSJPKTMWQPKS-UHFFFAOYSA-N c(cc1)ccc1-[n]1nc(-c(cc2)ccc2-c2cc(cccc3)c3cc2)nc1-c1ccc(cc2)c3c1ccc1c3c2ccc1 Chemical compound c(cc1)ccc1-[n]1nc(-c(cc2)ccc2-c2cc(cccc3)c3cc2)nc1-c1ccc(cc2)c3c1ccc1c3c2ccc1 BPBSJPKTMWQPKS-UHFFFAOYSA-N 0.000 description 1
- CVZWJOUQDIYCKH-UHFFFAOYSA-N c(cc1)ccc1-[n]1nc(-c2c(ccc3c4c(cc5)ccc3)c4c5cc2)nc1-c(cc1)ccc1-c1cc(cccc2)c2cc1 Chemical compound c(cc1)ccc1-[n]1nc(-c2c(ccc3c4c(cc5)ccc3)c4c5cc2)nc1-c(cc1)ccc1-c1cc(cccc2)c2cc1 CVZWJOUQDIYCKH-UHFFFAOYSA-N 0.000 description 1
- WZCQFRYAYCWJTD-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c(cc1)ccc1-c(nc1-c2c(cccc3)c3ccc2)n[n]1-c1c(cccc2)c2ccc1 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c(cc1)ccc1-c(nc1-c2c(cccc3)c3ccc2)n[n]1-c1c(cccc2)c2ccc1 WZCQFRYAYCWJTD-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05103497 | 2005-04-28 | ||
| EP05103497.3 | 2005-04-28 | ||
| EP05107906.9 | 2005-08-30 | ||
| EP05107906 | 2005-08-30 | ||
| PCT/EP2006/061670 WO2006114377A1 (en) | 2005-04-28 | 2006-04-19 | Electroluminescent device |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008539192A JP2008539192A (ja) | 2008-11-13 |
| JP2008539192A5 true JP2008539192A5 (enExample) | 2009-06-18 |
| JP5138582B2 JP5138582B2 (ja) | 2013-02-06 |
Family
ID=36443173
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008508194A Active JP5138582B2 (ja) | 2005-04-28 | 2006-04-19 | 電子発光装置 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9113536B2 (enExample) |
| EP (1) | EP1874740B1 (enExample) |
| JP (1) | JP5138582B2 (enExample) |
| KR (1) | KR101402633B1 (enExample) |
| CN (1) | CN101171239B (enExample) |
| TW (1) | TW200700535A (enExample) |
| WO (1) | WO2006114377A1 (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7651791B2 (en) | 2005-12-15 | 2010-01-26 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescence device and electroluminescence device employing the same |
| CN101331626B (zh) * | 2005-12-15 | 2011-08-17 | 出光兴产株式会社 | 有机电致发光元件用材料及使用其的有机电致发光元件 |
| US20080090834A1 (en) * | 2006-07-06 | 2008-04-17 | Pfizer Inc | Selective azole pde10a inhibitor compounds |
| KR101764599B1 (ko) * | 2009-03-31 | 2017-08-03 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 트리아졸 유도체, 트리아졸 유도체를 사용한 발광 소자, 발광 장치, 조명 장치 및 전자 기기 |
| JP5624784B2 (ja) * | 2009-03-31 | 2014-11-12 | 株式会社半導体エネルギー研究所 | ヘテロ芳香環を有する誘導体、ヘテロ芳香環を有する誘導体を用いた発光素子、発光装置、照明装置、電子機器 |
| US8993125B2 (en) * | 2010-05-21 | 2015-03-31 | Semiconductor Energy Laboratory Co., Ltd. | Triazole derivative, and light-emitting element, light-emitting device, electronic device and lighting device using the triazole derivative |
| WO2012004765A2 (en) * | 2010-07-08 | 2012-01-12 | Basf Se | Use of dibenzofurans and dibenzothiophenes substituted by nitrogen-bonded five-membered heterocyclic rings in organic electronics |
| US9067919B2 (en) | 2010-07-08 | 2015-06-30 | Basf Se | Use of dibenzofurans and dibenzothiophenes substituted by nitrogen-bonded five-membered heterocyclic rings in organic electronics |
| JP5699524B2 (ja) * | 2010-10-21 | 2015-04-15 | コニカミノルタ株式会社 | 有機光電変換素子および太陽電池 |
| TWI520952B (zh) * | 2010-11-18 | 2016-02-11 | 半導體能源研究所股份有限公司 | 二唑衍生物，及使用該二唑衍生物之發光元件，發光裝置，電子裝置，和照明裝置 |
| KR101893624B1 (ko) * | 2010-11-26 | 2018-08-30 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 유기금속 착물, 발광 엘리먼트, 발광 디바이스, 전자 디바이스 및 조명 디바이스 |
| KR101910030B1 (ko) * | 2010-11-30 | 2018-10-19 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 벤조옥사졸 유도체, 발광 소자, 발광 장치, 전자기기 및 조명 장치 |
| WO2012077902A2 (ko) | 2010-12-08 | 2012-06-14 | 제일모직 주식회사 | 유기광전자소자용 화합물, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
| KR20130009619A (ko) * | 2011-07-06 | 2013-01-23 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 표시 장치, 조명 장치 및 전자 기기 |
| CN105143198A (zh) * | 2013-02-26 | 2015-12-09 | 保土谷化学工业株式会社 | 新型萘三唑衍生物和有机电致发光器件 |
| CN103772305A (zh) * | 2014-01-14 | 2014-05-07 | 天津师范大学 | 氧醚三氮唑化合物及其制备方法与应用 |
| CN106687561A (zh) * | 2014-09-26 | 2017-05-17 | Udc爱尔兰有限责任公司 | 具有高效率的荧光有机发光元件 |
| JP2016121288A (ja) * | 2014-12-25 | 2016-07-07 | Jnc株式会社 | 光学的に等方性の液晶媒体及び光素子 |
| JP7016535B2 (ja) | 2015-10-26 | 2022-02-07 | オーティーアイ ルミオニクス インコーポレーテッド | パターン化されたコーティングを含む表面およびデバイス上のコーティングをパターン化する方法 |
| KR102780240B1 (ko) | 2017-04-26 | 2025-03-14 | 오티아이 루미오닉스 인크. | 표면의 코팅을 패턴화하는 방법 및 패턴화된 코팅을 포함하는 장치 |
| CN109912575B (zh) * | 2017-12-12 | 2020-07-28 | 中节能万润股份有限公司 | 一种以含氮五元杂环为核心的化合物及其在有机电致发光器件上的应用 |
| CN109912609A (zh) * | 2017-12-12 | 2019-06-21 | 江苏三月光电科技有限公司 | 一种以含氮五元杂环为母核的化合物及其在有机电致发光器件上的应用 |
| KR102536247B1 (ko) * | 2017-12-22 | 2023-05-25 | 삼성디스플레이 주식회사 | 헤테로고리 화합물 및 이를 포함한 유기 발광 소자 |
| US11751415B2 (en) | 2018-02-02 | 2023-09-05 | Oti Lumionics Inc. | Materials for forming a nucleation-inhibiting coating and devices incorporating same |
| KR20250160226A (ko) | 2019-03-07 | 2025-11-11 | 오티아이 루미오닉스 인크. | 핵생성 억제 코팅물 형성용 재료 및 이를 포함하는 디바이스 |
| KR102831863B1 (ko) | 2019-04-18 | 2025-07-10 | 오티아이 루미오닉스 인크. | 핵 생성 억제 코팅 형성용 물질 및 이를 포함하는 디바이스 |
| US12069938B2 (en) | 2019-05-08 | 2024-08-20 | Oti Lumionics Inc. | Materials for forming a nucleation-inhibiting coating and devices incorporating same |
| JP2023553379A (ja) | 2020-12-07 | 2023-12-21 | オーティーアイ ルミオニクス インコーポレーテッド | 核形成抑制被膜及び下地金属被膜を用いた導電性堆積層のパターニング |
| CN115583941B (zh) * | 2022-12-09 | 2023-05-23 | 华南理工大学 | 一类含三氮唑的蒽基蓝光有机半导体材料及其制备方法与应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1132927B (de) | 1961-04-25 | 1962-07-12 | Basf Ag | Verfahren zur Herstellung von 2, 3, 5-trisubstituierten 1, 2, 4-Triazolen |
| CH542212A (de) | 1966-09-23 | 1973-09-30 | Ciba Geigy Ag | Verfahren zur Herstellung heterocyclischer Äthylendoppelbindungen enthaltender Verbindungen |
| US3592656A (en) * | 1968-09-03 | 1971-07-13 | Eastman Kodak Co | Photographic silver halide materials supersensitized with a combination of a triazole and a cyanine dye |
| JPS5235300A (en) | 1975-09-12 | 1977-03-17 | Sakai Chem Ind Co Ltd | Curing agents for epoxy resins |
| DD129908A1 (de) | 1977-02-28 | 1978-02-15 | Juergen Liebscher | Verfahren zur herstellung von 1,3,5-trisubstituierten 1,2,4-triazolen |
| EP0036711B1 (en) * | 1980-03-22 | 1985-12-04 | Fbc Limited | Pesticidal heterocyclic compounds, processes for preparing them, compositions containing them, and their use |
| JPS56164464A (en) | 1980-05-21 | 1981-12-17 | Tatsuo Nogi | Parallel processing computer |
| US4769292A (en) * | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
| JP2000100570A (ja) * | 1998-09-25 | 2000-04-07 | Toray Ind Inc | 発光素子 |
| EP1099695A1 (en) | 1999-11-09 | 2001-05-16 | Laboratoire Theramex S.A. | 5-aryl-1H-1,2,4-triazole compounds as inhibitors of cyclooxygenase-2 and pharmaceutical compositions containing them |
| JP4994564B2 (ja) * | 2001-03-02 | 2012-08-08 | ザ、トラスティーズ オブ プリンストン ユニバーシティ | 二重ドープ層燐光有機発光装置 |
| JP2003005356A (ja) * | 2001-06-20 | 2003-01-08 | Fuji Photo Film Co Ltd | 電子線又はｘ線用ネガ型レジスト組成物 |
| JP2003109765A (ja) * | 2001-09-28 | 2003-04-11 | Canon Inc | 有機発光素子 |
| US6916554B2 (en) * | 2002-11-06 | 2005-07-12 | The University Of Southern California | Organic light emitting materials and devices |
| JP4631259B2 (ja) * | 2002-10-03 | 2011-02-16 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子及び表示装置 |
| JP4590825B2 (ja) * | 2003-02-21 | 2010-12-01 | コニカミノルタホールディングス株式会社 | 白色発光有機エレクトロルミネッセンス素子 |
| JP2005044790A (ja) * | 2003-07-08 | 2005-02-17 | Konica Minolta Holdings Inc | 有機エレクトロルミネッセンス素子、照明装置および表示装置 |
-
2006
- 2006-04-19 CN CN2006800147372A patent/CN101171239B/zh active Active
- 2006-04-19 WO PCT/EP2006/061670 patent/WO2006114377A1/en not_active Ceased
- 2006-04-19 KR KR1020077027653A patent/KR101402633B1/ko active Active
- 2006-04-19 EP EP06743343.3A patent/EP1874740B1/en active Active
- 2006-04-19 JP JP2008508194A patent/JP5138582B2/ja active Active
- 2006-04-19 US US11/919,105 patent/US9113536B2/en active Active
- 2006-04-27 TW TW095115052A patent/TW200700535A/zh unknown
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