JP2017530969A5 - - Google Patents
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- JP2017530969A5 JP2017530969A5 JP2017514891A JP2017514891A JP2017530969A5 JP 2017530969 A5 JP2017530969 A5 JP 2017530969A5 JP 2017514891 A JP2017514891 A JP 2017514891A JP 2017514891 A JP2017514891 A JP 2017514891A JP 2017530969 A5 JP2017530969 A5 JP 2017530969A5
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- JP
- Japan
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- aromatic
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- 125000003118 aryl group Chemical group 0.000 claims description 123
- 125000004432 carbon atom Chemical group C* 0.000 claims description 77
- 229910052799 carbon Inorganic materials 0.000 claims description 69
- 229910052731 fluorine Inorganic materials 0.000 claims description 67
- 229910052717 sulfur Inorganic materials 0.000 claims description 58
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 53
- 229910052805 deuterium Inorganic materials 0.000 claims description 52
- 125000003342 alkenyl group Chemical group 0.000 claims description 46
- 229910052801 chlorine Inorganic materials 0.000 claims description 46
- 125000003545 alkoxy group Chemical group 0.000 claims description 44
- 125000000304 alkynyl group Chemical group 0.000 claims description 44
- 229910052794 bromium Inorganic materials 0.000 claims description 44
- 229910052740 iodine Inorganic materials 0.000 claims description 44
- 229910052760 oxygen Inorganic materials 0.000 claims description 44
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 44
- 238000004132 cross linking Methods 0.000 claims description 35
- 125000004122 cyclic group Chemical group 0.000 claims description 34
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 33
- 125000002950 monocyclic group Chemical group 0.000 claims description 33
- 125000000732 arylene group Chemical group 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 31
- 125000001424 substituent group Chemical group 0.000 claims description 31
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 125000001931 aliphatic group Chemical group 0.000 claims description 22
- 125000004104 aryloxy group Chemical group 0.000 claims description 22
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 22
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 22
- 125000005240 diheteroarylamino group Chemical group 0.000 claims description 22
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims description 22
- 125000003367 polycyclic group Chemical group 0.000 claims description 22
- 125000004986 diarylamino group Chemical group 0.000 claims description 21
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 11
- 125000001072 heteroaryl group Chemical group 0.000 claims description 11
- 125000006413 ring segment Chemical group 0.000 claims description 10
- 150000001540 azides Chemical class 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 239000000539 dimer Substances 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 description 38
- 125000004450 alkenylene group Chemical group 0.000 description 12
- 125000002947 alkylene group Chemical group 0.000 description 12
- 125000004419 alkynylene group Chemical group 0.000 description 12
- 125000005549 heteroarylene group Chemical group 0.000 description 10
- 229910052698 phosphorus Inorganic materials 0.000 description 5
- 239000003377 acid catalyst Substances 0.000 description 3
- 230000005693 optoelectronics Effects 0.000 description 3
- LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical class C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000004404 heteroalkyl group Chemical group 0.000 description 2
- 125000005241 heteroarylamino group Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000000269 nucleophilic effect Effects 0.000 description 2
- 125000003107 substituted aryl group Chemical group 0.000 description 2
- UXJHQQLYKUVLIE-UHFFFAOYSA-N 1,2-dihydroacridine Chemical class C1=CC=C2N=C(C=CCC3)C3=CC2=C1 UXJHQQLYKUVLIE-UHFFFAOYSA-N 0.000 description 1
- ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 1,2-dihydrophenazine Chemical class C1=CC=C2N=C(C=CCC3)C3=NC2=C1 ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- XKLNOVWDVMWTOB-UHFFFAOYSA-N 2,3,4,9-tetrahydro-1h-carbazole Chemical class N1C2=CC=CC=C2C2=C1CCCC2 XKLNOVWDVMWTOB-UHFFFAOYSA-N 0.000 description 1
- UJOBWOGCFQCDNV-UHFFFAOYSA-N Carbazole Natural products C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241001024304 Mino Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001344 alkene derivatives Chemical class 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N benzopyrrole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- 125000000609 carbazolyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000012650 click reaction Methods 0.000 description 1
- 238000001194 electroluminescence spectrum Methods 0.000 description 1
- 239000011737 fluorine Substances 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
- 150000002475 indoles Chemical class 0.000 description 1
- 125000003387 indolinyl group Chemical class N1(CCC2=CC=CC=C12)* 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 125000001644 phenoxazinyl group Chemical class C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- 125000005543 phthalimide group Chemical group 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14185118.8 | 2014-09-17 | ||
| EP14185118 | 2014-09-17 | ||
| EP14193686.4 | 2014-11-18 | ||
| EP14193686 | 2014-11-18 | ||
| PCT/EP2015/071309 WO2016042070A1 (de) | 2014-09-17 | 2015-09-17 | Organische moleküle zur verwendung als emitter |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017530969A JP2017530969A (ja) | 2017-10-19 |
| JP2017530969A5 true JP2017530969A5 (enExample) | 2019-11-21 |
| JP6954833B2 JP6954833B2 (ja) | 2021-10-27 |
Family
ID=54291250
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017514891A Active JP6954833B2 (ja) | 2014-09-17 | 2015-09-17 | エミッタとして使用するための有機分子 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10651394B2 (enExample) |
| EP (2) | EP3246373B1 (enExample) |
| JP (1) | JP6954833B2 (enExample) |
| KR (1) | KR102251715B1 (enExample) |
| CN (1) | CN106715644B (enExample) |
| TW (1) | TWI688555B (enExample) |
| WO (1) | WO2016042070A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10074805B2 (en) * | 2014-09-22 | 2018-09-11 | Udc Ireland Limited | Fluorescent organic light emitting elements having high efficiency |
| DE102016104929A1 (de) * | 2016-03-16 | 2017-09-21 | Cynora Gmbh | Organische Moleküle zur Verwendung als Emitter |
| KR102545509B1 (ko) * | 2016-06-02 | 2023-06-21 | 삼성디스플레이 주식회사 | 다환 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| JP6942127B2 (ja) * | 2016-07-08 | 2021-09-29 | メルク、パテント、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ ＧｍｂＨ | 有機エレクトロルミネッセンス素子、表示装置、照明装置 |
| WO2018024724A1 (de) * | 2016-08-04 | 2018-02-08 | Cynora Gmbh | Organische moleküle zur verwendung in optoelektronischen vorrichtungen |
| EP3279193B1 (de) * | 2016-08-04 | 2019-05-08 | Cynora Gmbh | Phthalimid und carbazol oder dessen analoge enthaltende verbindungen zur verwendung in organischen optoelektronischen vorrichtungen |
| EP3279194A1 (de) * | 2016-08-04 | 2018-02-07 | Cynora Gmbh | Organische moleküle zur verwendung in organischen optoelektronischen vorrichtungen |
| CN106800526B (zh) * | 2016-12-15 | 2019-01-29 | 中节能万润股份有限公司 | 一种以环状二酮为核心的有机电致发光材料及其应用 |
| CN106831745B (zh) * | 2016-12-30 | 2020-01-14 | 上海天马有机发光显示技术有限公司 | 一种有机电致发光材料以及有机光电装置 |
| DE102017102869A1 (de) | 2017-02-14 | 2018-08-16 | Cynora Gmbh | Organische Elektrolumineszenzvorrichtung |
| DE102017107427B4 (de) * | 2017-04-06 | 2018-12-13 | Cynora Gmbh | Organische Moleküle, insbesondere zur Verwendung in organischen optoelektronischen Vorrichtungen |
| CN106966954A (zh) * | 2017-04-14 | 2017-07-21 | 中国科学院化学研究所 | 一种热激活延迟荧光材料及有机电致发光器件 |
| CN107256927B (zh) * | 2017-06-13 | 2020-01-24 | 上海天马有机发光显示技术有限公司 | 有机发光器件和显示装置 |
| CN109422674B (zh) * | 2017-08-25 | 2024-03-22 | 三星显示有限公司 | 有机分子，特别是用于光电子器件的有机分子 |
| KR102567881B1 (ko) | 2017-11-15 | 2023-08-18 | 삼성디스플레이 주식회사 | 함질소 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| CN108117506A (zh) * | 2017-12-19 | 2018-06-05 | 中国科学院化学研究所 | 一种基于手性1,2-环己二胺的光学纯热激活延迟荧光材料及其制备方法与应用 |
| KR102176874B1 (ko) * | 2018-02-23 | 2020-11-10 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함하는 유기 발광 소자 |
| CN110467609B (zh) * | 2019-07-04 | 2023-01-10 | 华南师范大学 | 一种同时具有圆偏振发光和热激活延迟荧光发射的聚集诱导发光材料及其制备方法与应用 |
| CN111303010B (zh) * | 2019-11-07 | 2023-05-09 | 中山大学 | 一种含酰亚胺结构的有机室温磷光材料、制备方法及其应用 |
| CN111039936A (zh) * | 2019-12-30 | 2020-04-21 | 陕西莱特光电材料股份有限公司 | 苯并恶嗪类化合物、有机电致发光器件以及电子装置 |
| KR102776384B1 (ko) | 2020-05-06 | 2025-03-10 | 삼성디스플레이 주식회사 | 발광 소자 및 이를 포함하는 전자 장치 |
| JP2023131962A (ja) * | 2022-03-10 | 2023-09-22 | 株式会社ダイセル | 有機半導体材料 |
| CN114957093A (zh) * | 2022-05-30 | 2022-08-30 | 南京邮电大学 | 一种具有室温磷光的有机物及其制备方法和应用 |
| CN119118905B (zh) * | 2024-09-11 | 2025-07-01 | 香港中文大学（深圳） | 一种基于碳-氮轴手性的圆偏振tadf材料 |
| CN118955357B (zh) * | 2024-10-15 | 2025-01-03 | 香港中文大学（深圳） | 一种红光发光材料及其制备方法与应用 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6867198B2 (en) * | 1999-12-16 | 2005-03-15 | Eli Lilly And Company | Agents and methods for the treatment of proliferative diseases |
| JP4809656B2 (ja) * | 2005-09-29 | 2011-11-09 | 富士フイルム株式会社 | ナフタロシアニン色素およびその製造方法 |
| JP2007191636A (ja) * | 2006-01-20 | 2007-08-02 | Fujifilm Corp | インク組成物、インクジェット記録用インク、インクセットおよびインクジェット記録方法 |
| JP5189077B2 (ja) * | 2006-04-13 | 2013-04-24 | ユニバーシティ オブ サザン カリフォルニア | フタルイミド化合物を用いた有機電子デバイス |
| TWI420722B (zh) | 2008-01-30 | 2013-12-21 | 歐斯朗奧托半導體股份有限公司 | 具有封裝單元之裝置 |
| EP2356372B1 (de) | 2008-12-11 | 2016-08-10 | OSRAM OLED GmbH | Organische leuchtdiode und beleuchtungsmittel |
| US8048541B2 (en) * | 2008-12-17 | 2011-11-01 | City University Of Hong Kong | Organic electroluminescence device |
| DE102009024411A1 (de) | 2009-03-24 | 2010-09-30 | Osram Opto Semiconductors Gmbh | Dünnschichtverkapselung für ein optoelektronisches Bauelement, Verfahren zu dessen Herstellung und optoelektronisches Bauelement |
| DE102009030475A1 (de) | 2009-06-24 | 2011-01-05 | Hartmut Prof. Dr. Yersin | Kupfer-Komplexe für optoelektronische Anwendungen |
| WO2011033023A1 (en) | 2009-09-18 | 2011-03-24 | Osram Opto Semiconductors Gmbh | Organic electronic device and dopant for doping an organic semiconducting matrix material |
| DE102009047880A1 (de) | 2009-09-30 | 2011-03-31 | Osram Opto Semiconductors Gmbh | Organische elektronische Vorrichtung und Verfahren zu dessen Herstellung |
| CN101787129A (zh) * | 2010-03-04 | 2010-07-28 | 南京航空航天大学 | 可溶性耐高温芳香族聚酰亚胺及其制备方法 |
| DE102010013495A1 (de) | 2010-03-31 | 2011-10-06 | Siemens Aktiengesellschaft | Dotierstoff für eine Lochleiterschicht für organische Halbleiterbauelemente und Verwendung dazu |
| CN102086181A (zh) * | 2011-01-21 | 2011-06-08 | 南京航空航天大学 | 2,2'-二芳基-4,4',5,5'-联苯四酸二酐单体合成方法 |
| CN102344404A (zh) * | 2011-07-07 | 2012-02-08 | 南京邮电大学 | 基于邻苯二甲酰亚胺的三聚氰胺荧光传感器材料 |
| JP5594750B2 (ja) | 2012-05-17 | 2014-09-24 | 国立大学法人九州大学 | 化合物、発光材料および有機発光素子 |
| DE102012209523A1 (de) | 2012-06-06 | 2013-12-12 | Osram Opto Semiconductors Gmbh | Hauptgruppenmetallkomplexe als p-Dotanden für organische elektronische Matrixmaterialien |
| DE102012209520A1 (de) | 2012-06-06 | 2013-12-12 | Osram Opto Semiconductors Gmbh | Metallkomplexe als p-Dotanden für organische elektronische Matrixmaterialien |
-
2015
- 2015-09-17 KR KR1020177005332A patent/KR102251715B1/ko active Active
- 2015-09-17 US US15/506,346 patent/US10651394B2/en active Active
- 2015-09-17 EP EP17176049.9A patent/EP3246373B1/de active Active
- 2015-09-17 EP EP15778218.6A patent/EP3137574B1/de active Active
- 2015-09-17 CN CN201580049835.9A patent/CN106715644B/zh active Active
- 2015-09-17 WO PCT/EP2015/071309 patent/WO2016042070A1/de not_active Ceased
- 2015-09-17 JP JP2017514891A patent/JP6954833B2/ja active Active
- 2015-09-17 TW TW104130838A patent/TWI688555B/zh active
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