JP2013511476A5 - - Google Patents
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- JP2013511476A5 JP2013511476A5 JP2012539209A JP2012539209A JP2013511476A5 JP 2013511476 A5 JP2013511476 A5 JP 2013511476A5 JP 2012539209 A JP2012539209 A JP 2012539209A JP 2012539209 A JP2012539209 A JP 2012539209A JP 2013511476 A5 JP2013511476 A5 JP 2013511476A5
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- 125000003118 aryl group Chemical group 0.000 claims description 35
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 125000001424 substituent group Chemical group 0.000 claims description 13
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 11
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 229910052717 sulfur Inorganic materials 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 229910052805 deuterium Inorganic materials 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000001072 heteroaryl group Chemical group 0.000 claims description 5
- 125000002950 monocyclic group Chemical group 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000001118 alkylidene group Chemical group 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000004437 phosphorous atom Chemical group 0.000 claims description 2
- 239000000463 material Substances 0.000 claims 4
- 230000004888 barrier function Effects 0.000 claims 3
- 230000000903 blocking effect Effects 0.000 claims 2
- 230000005525 hole transport Effects 0.000 claims 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
- HQALDKFFRYFTKP-UHFFFAOYSA-N 2-[4-[4-(2-benzyl-1-benzothiophen-3-yl)phenyl]-2-bromo-6-(3-methoxyphenyl)phenoxy]acetic acid Chemical compound COC1=CC=CC(C=2C(=C(Br)C=C(C=2)C=2C=CC(=CC=2)C=2C3=CC=CC=C3SC=2CC=2C=CC=CC=2)OCC(O)=O)=C1 HQALDKFFRYFTKP-UHFFFAOYSA-N 0.000 claims 1
- BPMFPOGUJAAYHL-UHFFFAOYSA-N 9H-Pyrido[2,3-b]indole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=N1 BPMFPOGUJAAYHL-UHFFFAOYSA-N 0.000 claims 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 125000000609 carbazolyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 150000001907 coumarones Chemical class 0.000 claims 1
- 150000004826 dibenzofurans Chemical class 0.000 claims 1
- IYYZUPMFVPLQIF-ALWQSETLSA-N dibenzothiophene Chemical class C1=CC=CC=2[34S]C3=C(C=21)C=CC=C3 IYYZUPMFVPLQIF-ALWQSETLSA-N 0.000 claims 1
- 230000005684 electric field Effects 0.000 claims 1
- 238000005401 electroluminescence Methods 0.000 claims 1
- 230000005669 field effect Effects 0.000 claims 1
- 150000002240 furans Chemical class 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- WUNJCKOTXFSWBK-UHFFFAOYSA-N indeno[2,1-a]carbazole Chemical class C1=CC=C2C=C3C4=NC5=CC=CC=C5C4=CC=C3C2=C1 WUNJCKOTXFSWBK-UHFFFAOYSA-N 0.000 claims 1
- 150000002475 indoles Chemical class 0.000 claims 1
- VVVPGLRKXQSQSZ-UHFFFAOYSA-N indolo[3,2-c]carbazole Chemical class C1=CC=CC2=NC3=C4C5=CC=CC=C5N=C4C=CC3=C21 VVVPGLRKXQSQSZ-UHFFFAOYSA-N 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000011159 matrix material Substances 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 108091008695 photoreceptors Proteins 0.000 claims 1
- 238000007363 ring formation reaction Methods 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 125000003003 spiro group Chemical group 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 239000010409 thin film Substances 0.000 claims 1
- 150000003577 thiophenes Chemical class 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000005309 thioalkoxy group Chemical group 0.000 description 4
- 125000005529 alkyleneoxy group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- 125000004475 heteroaralkyl group Chemical group 0.000 description 2
- 125000005553 heteroaryloxy group Chemical group 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000004419 alkynylene group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 210000002816 gill Anatomy 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009053836A DE102009053836A1 (de) | 2009-11-18 | 2009-11-18 | Materialien für organische Elektrolumineszenzvorrichtungen |
| DE102009053836.4 | 2009-11-18 | ||
| PCT/EP2010/006414 WO2011060867A1 (de) | 2009-11-18 | 2010-10-20 | Stickstoffhaltige kondensierte heterozyklen für oleds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013511476A JP2013511476A (ja) | 2013-04-04 |
| JP2013511476A5 true JP2013511476A5 (https=) | 2016-02-12 |
| JP6009356B2 JP6009356B2 (ja) | 2016-10-19 |
Family
ID=43560745
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012539209A Expired - Fee Related JP6009356B2 (ja) | 2009-11-18 | 2010-10-20 | Ｏｌｅｄのための窒素含有縮合ヘテロ環化合物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9012599B2 (https=) |
| JP (1) | JP6009356B2 (https=) |
| KR (1) | KR101781235B1 (https=) |
| CN (1) | CN102612518A (https=) |
| DE (2) | DE102009053836A1 (https=) |
| TW (1) | TW201134819A (https=) |
| WO (1) | WO2011060867A1 (https=) |
Families Citing this family (171)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009041289A1 (de) * | 2009-09-16 | 2011-03-17 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
| DE102010010481A1 (de) | 2010-03-06 | 2011-09-08 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
| DE102010012738A1 (de) | 2010-03-25 | 2011-09-29 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
| DE102010019306B4 (de) | 2010-05-04 | 2021-05-20 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
| JP2012082344A (ja) * | 2010-10-13 | 2012-04-26 | Sumitomo Chemical Co Ltd | 縮合芳香族化合物、有機半導体材料及び有機トランジスタ |
| DE102010048608A1 (de) | 2010-10-15 | 2012-04-19 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
| WO2012069121A1 (de) | 2010-11-24 | 2012-05-31 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
| DE102012000064B4 (de) | 2011-01-21 | 2026-01-22 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
| JP5845599B2 (ja) * | 2011-03-11 | 2016-01-20 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
| CN103477462B (zh) | 2011-04-05 | 2016-05-25 | 默克专利有限公司 | 有机电致发光器件 |
| JP6215192B2 (ja) | 2011-04-18 | 2017-10-18 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネッセンス素子用材料 |
| KR20140036279A (ko) * | 2011-06-01 | 2014-03-25 | 메르크 파텐트 게엠베하 | 하이브리드 양극성 ｔｆｔ들 |
| CN103619986B (zh) * | 2011-06-03 | 2017-02-08 | 默克专利有限公司 | 有机电致发光器件 |
| KR101887003B1 (ko) * | 2011-07-21 | 2018-08-13 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
| KR102051790B1 (ko) | 2011-08-22 | 2019-12-04 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스 |
| KR20130053846A (ko) * | 2011-11-16 | 2013-05-24 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
| US10305040B2 (en) | 2011-11-17 | 2019-05-28 | Merck Patent Gmbh | Spiro dihydroacridine derivatives and the use thereof as materials for organic electroluminescence devices |
| TWI606051B (zh) * | 2011-11-22 | 2017-11-21 | Ｕｄｃ愛爾蘭有限公司 | 有機電場發光元件、有機電場發光元件用材料以及使用該元件之發光裝置、顯示裝置、照明裝置及用於該元件之化合物 |
| JP5981770B2 (ja) * | 2012-01-23 | 2016-08-31 | ユー・ディー・シー アイルランド リミテッド | 有機電界発光素子、有機電界発光素子用電荷輸送材料、並びに、該素子を用いた発光装置、表示装置及び照明装置 |
| JP5926580B2 (ja) | 2012-03-01 | 2016-05-25 | ユー・ディー・シー アイルランド リミテッド | 有機電界発光素子、有機電界発光素子用材料、並びに、該素子を用いた発光装置、表示装置、照明装置及び該素子に用いられる化合物 |
| EP2828266B1 (de) | 2012-03-23 | 2017-10-18 | Merck Patent GmbH | 9,9'-spirobixanthenderivate für elektrolumineszenzvorrichtungen |
| CN104203920A (zh) * | 2012-04-10 | 2014-12-10 | 保土谷化学工业株式会社 | 具有9,10-二氢吖啶环结构的化合物以及有机电致发光器件 |
| JP6009817B2 (ja) * | 2012-05-22 | 2016-10-19 | ユー・ディー・シー アイルランド リミテッド | 電荷輸送材料、有機電界発光素子、発光装置、表示装置および照明装置 |
| KR101640285B1 (ko) * | 2012-05-31 | 2016-07-15 | 주식회사 엘지화학 | 신규한 화합물 및 이를 이용한 유기 발광 소자 |
| KR102058262B1 (ko) * | 2012-09-03 | 2019-12-20 | 호도가야 가가쿠 고교 가부시키가이샤 | 인데노 아크리단 환 구조를 가지는 화합물 및 유기 일렉트로루미네선스 소자 |
| WO2014046495A1 (ko) * | 2012-09-21 | 2014-03-27 | 주식회사 엘엠에스 | 신규 구조의 발광 소자 및 이를 포함하는 전자 장치 |
| KR101390362B1 (ko) * | 2012-09-21 | 2014-04-30 | 주식회사 엘엠에스 | 신규한 화합물, 이를 포함하는 발광 소자 및 전자 장치 |
| CN102945928A (zh) * | 2012-12-06 | 2013-02-27 | 吉林大学 | 一种光谱可调且色坐标稳定的白光有机电致发光器件 |
| CN103130812B (zh) * | 2013-03-05 | 2014-12-24 | 华东师范大学 | 一种吲哚并[3,2,1-jk]咔唑衍生物及其制备方法和应用 |
| JP6576929B2 (ja) * | 2013-09-11 | 2019-09-18 | メルク パテント ゲーエムベーハー | ヘテロ環化合物 |
| KR102372950B1 (ko) * | 2014-05-02 | 2022-03-14 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| KR102419246B1 (ko) | 2014-06-25 | 2022-07-08 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
| KR102420202B1 (ko) | 2014-06-27 | 2022-07-14 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 전계 발광 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| KR102419711B1 (ko) | 2014-07-09 | 2022-07-13 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| JP6065933B2 (ja) * | 2015-04-01 | 2017-01-25 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子の製造方法、表示装置、並びに照明装置 |
| JP6651712B2 (ja) * | 2015-05-15 | 2020-02-19 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、その製造方法、表示装置、照明装置、有機エレクトロルミネッセンス素子材料及び新規化合物 |
| JP2018525331A (ja) | 2015-06-10 | 2018-09-06 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネッセンス素子のための材料 |
| CN107922359A (zh) | 2015-07-30 | 2018-04-17 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
| US10211411B2 (en) | 2015-08-25 | 2019-02-19 | Arizona Board Of Regents On Behalf Of Arizona State University | Thermally activated delayed fluorescent material based on 9,10-dihydro-9,9-dimethylacridine analogues for prolonging device longevity |
| KR102678422B1 (ko) | 2015-10-27 | 2024-06-25 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
| CN105348300B (zh) * | 2015-11-10 | 2018-04-10 | 中节能万润股份有限公司 | 一种有机光电材料及其制备方法和用途 |
| CN105693749A (zh) * | 2016-03-09 | 2016-06-22 | 中节能万润股份有限公司 | 一种含有吩噻嗪结构的有机光电材料及其应用 |
| KR101834433B1 (ko) | 2016-06-08 | 2018-03-05 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함하는 유기발광 소자 |
| KR102477259B1 (ko) * | 2016-07-18 | 2022-12-14 | 삼성디스플레이 주식회사 | 유기 전계 발광 표시 장치 |
| TW201833118A (zh) * | 2016-11-22 | 2018-09-16 | 德商麥克專利有限公司 | 用於電子裝置之材料 |
| WO2018095393A1 (zh) * | 2016-11-23 | 2018-05-31 | 广州华睿光电材料有限公司 | 有机化合物、有机混合物、有机电子器件 |
| WO2018104194A1 (de) | 2016-12-05 | 2018-06-14 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
| KR20190086028A (ko) | 2016-12-05 | 2019-07-19 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
| CN110049986A (zh) | 2017-01-04 | 2019-07-23 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
| KR102559144B1 (ko) | 2017-01-30 | 2023-07-24 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
| TW201835075A (zh) | 2017-02-14 | 2018-10-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
| US10312455B2 (en) | 2017-03-26 | 2019-06-04 | Feng-wen Yen | Delayed fluorescence material for organic electroluminescence device |
| US10615349B2 (en) | 2017-05-19 | 2020-04-07 | Arizona Board Of Regents On Behalf Of Arizona State University | Donor-acceptor type thermally activated delayed fluorescent materials based on imidazo[1,2-F]phenanthridine and analogues |
| US10392387B2 (en) | 2017-05-19 | 2019-08-27 | Arizona Board Of Regents On Behalf Of Arizona State University | Substituted benzo[4,5]imidazo[1,2-a]phenanthro[9,10-c][1,8]naphthyridines, benzo[4,5]imidazo[1,2-a]phenanthro[9,10-c][1,5]naphthyridines and dibenzo[f,h]benzo[4,5]imidazo[2,1-a]pyrazino[2,3-c]isoquinolines as thermally assisted delayed fluorescent materials |
| WO2019081391A1 (de) | 2017-10-24 | 2019-05-02 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
| WO2019111971A1 (ja) | 2017-12-06 | 2019-06-13 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子及び新規化合物 |
| US10249832B1 (en) | 2017-12-06 | 2019-04-02 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and novel compound |
| TWI811290B (zh) | 2018-01-25 | 2023-08-11 | 德商麥克專利有限公司 | 用於有機電致發光裝置的材料 |
| US12419192B2 (en) | 2018-06-07 | 2025-09-16 | Merck Patent Gmbh | Organic electroluminescence devices |
| WO2020011686A1 (de) | 2018-07-09 | 2020-01-16 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
| CN108997345B (zh) * | 2018-08-20 | 2024-08-02 | 上海弗屈尔光电科技有限公司 | 一种氮杂螺环化合物及含有该化合物的有机光电器件 |
| US10593889B1 (en) | 2018-09-26 | 2020-03-17 | Idemitsu Kosan Co., Ltd. | Compound and organic electroluminescence device |
| CN112867709A (zh) | 2018-11-06 | 2021-05-28 | 默克专利有限公司 | 作为用于oled的有机电致发光材料的5,6-二苯基-5,6-二氢-二苯并[c,e][1,2]氮杂磷杂苯和6-苯基-6h-二苯并[c,e][1,2]噻嗪-5,5-二氧化物衍生物及类似化合物 |
| KR102845628B1 (ko) | 2018-11-15 | 2025-08-13 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
| CN110759910A (zh) * | 2018-12-06 | 2020-02-07 | 广州华睿光电材料有限公司 | 吡啶化合物及其用途 |
| KR20200075193A (ko) | 2018-12-17 | 2020-06-26 | 삼성디스플레이 주식회사 | 축합환 화합물, 이를 포함하는 유기 발광 소자 및 이를 포함하는 표시 장치 |
| TW202039493A (zh) | 2018-12-19 | 2020-11-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
| EP3938367A1 (de) | 2019-03-12 | 2022-01-19 | Merck Patent GmbH | Materialien für organische elektrolumineszenzvorrichtungen |
| KR20210141593A (ko) | 2019-03-20 | 2021-11-23 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 재료 |
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-
2009
- 2009-11-18 DE DE102009053836A patent/DE102009053836A1/de not_active Withdrawn
-
2010
- 2010-10-20 US US13/510,425 patent/US9012599B2/en active Active
- 2010-10-20 CN CN2010800523644A patent/CN102612518A/zh active Pending
- 2010-10-20 DE DE112010004482T patent/DE112010004482A5/de not_active Withdrawn
- 2010-10-20 JP JP2012539209A patent/JP6009356B2/ja not_active Expired - Fee Related
- 2010-10-20 WO PCT/EP2010/006414 patent/WO2011060867A1/de not_active Ceased
- 2010-10-20 KR KR1020127015799A patent/KR101781235B1/ko active Active
- 2010-11-15 TW TW099139205A patent/TW201134819A/zh unknown
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