JP2017059808A5 - - Google Patents
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- JP2017059808A5 JP2017059808A5 JP2016055831A JP2016055831A JP2017059808A5 JP 2017059808 A5 JP2017059808 A5 JP 2017059808A5 JP 2016055831 A JP2016055831 A JP 2016055831A JP 2016055831 A JP2016055831 A JP 2016055831A JP 2017059808 A5 JP2017059808 A5 JP 2017059808A5
- Authority
- JP
- Japan
- Prior art keywords
- organic
- substituent
- material according
- group
- general formula
- 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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- 239000000463 material Substances 0.000 claims description 22
- 125000001424 substituent group Chemical group 0.000 claims description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000002019 doping agent Substances 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 6
- 125000003107 substituted aryl group Chemical group 0.000 claims 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 4
- 239000010410 layer Substances 0.000 claims 4
- 125000001769 aryl amino group Chemical group 0.000 claims 2
- 239000012044 organic layer Substances 0.000 claims 2
- 230000003111 delayed effect Effects 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 2
- 229910003437 indium oxide Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- -1 ureido , Sulfinyl group Chemical group 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- MVWPVABZQQJTPL-UHFFFAOYSA-N 2,3-diphenylcyclohexa-2,5-diene-1,4-dione Chemical class O=C1C=CC(=O)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 MVWPVABZQQJTPL-UHFFFAOYSA-N 0.000 description 1
- STTGYIUESPWXOW-UHFFFAOYSA-N 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline Chemical compound C=12C=CC3=C(C=4C=CC=CC=4)C=C(C)N=C3C2=NC(C)=CC=1C1=CC=CC=C1 STTGYIUESPWXOW-UHFFFAOYSA-N 0.000 description 1
- ZYASLTYCYTYKFC-UHFFFAOYSA-N 9-methylidenefluorene Chemical class C1=CC=C2C(=C)C3=CC=CC=C3C2=C1 ZYASLTYCYTYKFC-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical compound [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
- 150000008425 anthrones Chemical class 0.000 description 1
- 229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 description 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 1
- 125000005110 aryl thio group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 150000005041 phenanthrolines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 150000003252 quinoxalines Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- IBBLKSWSCDAPIF-UHFFFAOYSA-N thiopyran Chemical compound S1C=CC=C=C1 IBBLKSWSCDAPIF-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2015125942 | 2015-06-23 | ||
| JP2015125942 | 2015-06-23 | ||
| JP2015182242 | 2015-09-15 | ||
| JP2015182242 | 2015-09-15 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017059808A JP2017059808A (ja) | 2017-03-23 |
| JP2017059808A5 true JP2017059808A5 (enExample) | 2019-02-14 |
| JP6660782B2 JP6660782B2 (ja) | 2020-03-11 |
Family
ID=57584793
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016055831A Active JP6660782B2 (ja) | 2015-06-23 | 2016-03-18 | 有機ｅｌ材料およびそれを用いた有機ｅｌ素子 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20190296246A1 (enExample) |
| EP (1) | EP3316328A4 (enExample) |
| JP (1) | JP6660782B2 (enExample) |
| WO (1) | WO2016208240A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102017102662B4 (de) * | 2017-02-10 | 2020-12-10 | Cynora Gmbh | Organische Moleküle, insbesondere zur Verwendung in organischen optoelektronischen Vorrichtungen |
| JP7267563B2 (ja) * | 2017-06-27 | 2023-05-02 | 株式会社Kyulux | 発光材料、化合物、遅延蛍光体および発光素子 |
| WO2019004254A1 (ja) * | 2017-06-27 | 2019-01-03 | 株式会社Ｋｙｕｌｕｘ | 発光材料、化合物、遅延蛍光体および発光素子 |
| GB201717193D0 (en) * | 2017-10-19 | 2017-12-06 | Univ Durham | Thermally activated delayed fluorescence molecules, materials comprising said molecules, and devices comprising said materials |
| CN109912565A (zh) * | 2017-12-13 | 2019-06-21 | 江苏三月光电科技有限公司 | 一种以氰基氮杂苯为核心的化合物及其在有机电致发光器件中的应用 |
| KR102637108B1 (ko) * | 2018-10-25 | 2024-02-19 | 삼성전자주식회사 | 축합환 화합물, 이를 포함한 조성물 및 이를 포함한 유기 발광 소자 |
| KR102388877B1 (ko) * | 2019-05-21 | 2022-04-21 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
| CN110078754A (zh) * | 2019-05-27 | 2019-08-02 | 上海天马有机发光显示技术有限公司 | 化合物、显示面板以及显示装置 |
| TWI742965B (zh) | 2020-12-18 | 2021-10-11 | 國立清華大學 | 含氰基吡啶化合物以及包含其的電激發光裝置 |
| CN114644617A (zh) * | 2020-12-18 | 2022-06-21 | 郑建鸿 | 含氰基吡啶化合物以及包含其的电激发光装置 |
| CN113224247B (zh) * | 2021-02-19 | 2025-02-14 | 冠能光电材料(深圳)有限责任公司 | 一种基于吡啶-3,5-二腈的电致发光材料及其在有机发光器件应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5624270B2 (ja) * | 2007-09-18 | 2014-11-12 | 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 |
| CN101412907A (zh) * | 2007-10-17 | 2009-04-22 | 中国科学院理化技术研究所 | 有机电致发光材料及其合成方法和用途 |
| US8101290B2 (en) * | 2007-10-17 | 2012-01-24 | Technical Institute Of Physics And Chemistry Of Chinese Academy Of Sciences | Organic compound having electron-transporting and/or hole-blocking performance and its use and OLEDs comprising the compound |
| WO2011002870A2 (en) * | 2009-07-01 | 2011-01-06 | E. I. Du Pont De Nemours And Company | Chrysene compounds for luminescent applications |
| CN102276525B (zh) * | 2010-06-09 | 2015-03-18 | 中国科学院理化技术研究所 | 三苯胺取代的吡啶衍生物及其制备方法和应用 |
| CN105051014B (zh) * | 2013-03-22 | 2017-12-19 | 默克专利有限公司 | 用于电子器件的材料 |
| KR102411748B1 (ko) * | 2014-03-17 | 2022-06-23 | 롬엔드하스전자재료코리아유한회사 | 전자 버퍼 재료 및 유기 전계 발광 소자 |
| JP2017518281A (ja) * | 2014-05-14 | 2017-07-06 | プレジデント アンド フェローズ オブ ハーバード カレッジ | 有機発光ダイオード材料 |
| CN103980193B (zh) * | 2014-05-27 | 2016-05-04 | 北京理工大学 | 2,6-二氨基-3,5-二氰基吡啶化合物的一锅法合成 |
-
2016
- 2016-03-18 EP EP16814011.9A patent/EP3316328A4/en not_active Withdrawn
- 2016-03-18 US US15/735,114 patent/US20190296246A1/en not_active Abandoned
- 2016-03-18 WO PCT/JP2016/058845 patent/WO2016208240A1/ja not_active Ceased
- 2016-03-18 JP JP2016055831A patent/JP6660782B2/ja active Active
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