JP2014527030A5 - - Google Patents
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- JP2014527030A5 JP2014527030A5 JP2014517751A JP2014517751A JP2014527030A5 JP 2014527030 A5 JP2014527030 A5 JP 2014527030A5 JP 2014517751 A JP2014517751 A JP 2014517751A JP 2014517751 A JP2014517751 A JP 2014517751A JP 2014527030 A5 JP2014527030 A5 JP 2014527030A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- copper
- atom
- branched
- cyclic
- 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.)
- Pending
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- 125000003118 aryl group Chemical group 0.000 claims 16
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 claims 15
- 125000004122 cyclic group Chemical group 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 10
- 125000001424 substituent group Chemical group 0.000 claims 9
- 229910052799 carbon Inorganic materials 0.000 claims 8
- 150000001721 carbon Chemical group 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- 230000005693 optoelectronics Effects 0.000 claims 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000000304 alkynyl group Chemical group 0.000 claims 5
- 150000001408 amides Chemical group 0.000 claims 5
- 229910052785 arsenic Inorganic materials 0.000 claims 5
- 239000003446 ligand Substances 0.000 claims 5
- KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical group O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 claims 5
- 229910052698 phosphorus Inorganic materials 0.000 claims 5
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 4
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical group [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 150000002466 imines Chemical group 0.000 claims 4
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 claims 4
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims 4
- CQDAMYNQINDRQC-UHFFFAOYSA-N oxatriazole Chemical compound C1=NN=NO1 CQDAMYNQINDRQC-UHFFFAOYSA-N 0.000 claims 4
- 125000004437 phosphorous atom Chemical group 0.000 claims 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims 4
- 150000003536 tetrazoles Chemical class 0.000 claims 4
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 4
- YGNGABUJMXJPIJ-UHFFFAOYSA-N thiatriazole Chemical compound C1=NN=NS1 YGNGABUJMXJPIJ-UHFFFAOYSA-N 0.000 claims 4
- 150000003852 triazoles Chemical class 0.000 claims 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- 229910052710 silicon Inorganic materials 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 230000005669 field effect Effects 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- 230000003287 optical effect Effects 0.000 claims 2
- 125000000061 phosphanyl group Chemical group [H]P([H])* 0.000 claims 2
- 229920000570 polyether Polymers 0.000 claims 2
- CXBDYQVECUFKRK-UHFFFAOYSA-N 1-methoxybutane Chemical compound CCCCOC CXBDYQVECUFKRK-UHFFFAOYSA-N 0.000 claims 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 1
- 239000006096 absorbing agent Substances 0.000 claims 1
- 150000001412 amines Chemical group 0.000 claims 1
- 125000001317 arsoryl group Chemical group *[As](*)(*)=O 0.000 claims 1
- 150000007942 carboxylates Chemical class 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- 150000004699 copper complex Chemical class 0.000 claims 1
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 1
- 229910052805 deuterium Inorganic materials 0.000 claims 1
- 230000002708 enhancing effect Effects 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000011159 matrix material Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 1
- 230000005855 radiation Effects 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 238000000859 sublimation Methods 0.000 claims 1
- 230000008022 sublimation Effects 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 0 CC1=NN=C(*)*1 Chemical compound CC1=NN=C(*)*1 0.000 description 4
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11171921 | 2011-06-29 | ||
| EP11171921.7 | 2011-06-29 | ||
| EP11173369.7 | 2011-07-08 | ||
| EP11173369 | 2011-07-08 | ||
| EP11179099A EP2540730A1 (de) | 2011-06-29 | 2011-08-26 | Kupfer(I)komplexe, insbesondere für optoelektronische Bauelemente |
| EP11179099.4 | 2011-08-26 | ||
| PCT/EP2012/062783 WO2013001086A1 (de) | 2011-06-29 | 2012-06-29 | Kupfer(i)komplexe, insbesondere für optoelektronische bauelemente |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2014527030A JP2014527030A (ja) | 2014-10-09 |
| JP2014527030A5 true JP2014527030A5 (enExample) | 2015-08-13 |
Family
ID=44816995
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014517751A Pending JP2014527030A (ja) | 2011-06-29 | 2012-06-29 | 特に光電子素子用の銅（ｉ）錯体 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9917265B2 (enExample) |
| EP (2) | EP2540730A1 (enExample) |
| JP (1) | JP2014527030A (enExample) |
| KR (1) | KR101942324B1 (enExample) |
| CN (1) | CN103748100B (enExample) |
| WO (1) | WO2013001086A1 (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009030475A1 (de) * | 2009-06-24 | 2011-01-05 | Hartmut Prof. Dr. Yersin | Kupfer-Komplexe für optoelektronische Anwendungen |
| CN103534260A (zh) * | 2011-05-13 | 2014-01-22 | 辛诺拉有限公司 | 铜(i)络合物，尤其用于光电组件 |
| EP2594571A1 (de) | 2011-11-16 | 2013-05-22 | Cynora GmbH | Kupfer-Komplexe für optoelektronische Anwendungen |
| KR102796297B1 (ko) | 2013-12-20 | 2025-04-17 | 유디씨 아일랜드 리미티드 | 매우 짧은 감쇠 시간을 갖는 고효율 ｏｌｅｄ 장치 |
| DE112015001925B4 (de) | 2014-04-24 | 2024-02-01 | Samsung Display Co., Ltd. | Verwendung eines Materials zur fälschungssicheren Markierung von Gegenständen, Stoffen oder Stoffgemischen sowie Verfahren zur fälschungssicheren Markierung |
| DE102015216658A1 (de) | 2014-09-02 | 2016-03-03 | Cynora Gmbh | Strukturell Stabilisierte Kupfer(I)-Komplexe |
| EP2993176A1 (de) | 2014-09-02 | 2016-03-09 | cynora GmbH | Metall(i)-komplexe für verbesserte leitfähigkeit |
| WO2016037963A1 (de) | 2014-09-08 | 2016-03-17 | Cynora Gmbh | Stabilisierte optisch aktive schicht und verfahren zur herstellung |
| WO2016037964A1 (de) | 2014-09-08 | 2016-03-17 | Cynora Gmbh | Verbesserte optisch aktive schicht und verfahren zur herstellung |
| WO2016041802A1 (en) | 2014-09-16 | 2016-03-24 | Cynora Gmbh | Light-emitting layer suitable for bright luminescence |
| CN111668392B (zh) | 2015-06-03 | 2024-01-23 | Udc 爱尔兰有限责任公司 | 具有极短衰减时间的高效oled装置 |
| CN107793438B (zh) * | 2017-08-29 | 2019-11-12 | 中山大学 | 一种铜（i）膦苯杂环配合物及其制备方法和应用 |
| US20220048836A1 (en) | 2018-09-12 | 2022-02-17 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
| TW202030902A (zh) | 2018-09-12 | 2020-08-16 | 德商麥克專利有限公司 | 電致發光裝置 |
| TWI826522B (zh) | 2018-09-12 | 2023-12-21 | 德商麥克專利有限公司 | 電致發光裝置 |
| US20220127286A1 (en) | 2019-03-04 | 2022-04-28 | Merck Patent Gmbh | Ligands for nano-sized materials |
| JP7598873B2 (ja) | 2019-04-11 | 2024-12-12 | 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 | 有機エレクトロルミネッセンス素子のための材料 |
| KR20220092590A (ko) | 2019-11-04 | 2022-07-01 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 재료 |
| TW202134252A (zh) | 2019-11-12 | 2021-09-16 | 德商麥克專利有限公司 | 有機電致發光裝置用材料 |
| TW202136181A (zh) | 2019-12-04 | 2021-10-01 | 德商麥克專利有限公司 | 有機電致發光裝置用的材料 |
| WO2021151922A1 (de) | 2020-01-29 | 2021-08-05 | Merck Patent Gmbh | Benzimidazol-derivate |
| US20230337537A1 (en) | 2020-03-23 | 2023-10-19 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
| KR20250110873A (ko) | 2022-11-17 | 2025-07-21 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4557651B2 (ja) * | 2003-10-01 | 2010-10-06 | キヤノン株式会社 | 発光性銅配位化合物及び有機発光素子 |
| JP4472438B2 (ja) * | 2004-06-15 | 2010-06-02 | 株式会社リコー | 画像形成装置 |
| JP2008063399A (ja) * | 2006-09-06 | 2008-03-21 | Canon Inc | 発光素子 |
| DE102009030475A1 (de) * | 2009-06-24 | 2011-01-05 | Hartmut Prof. Dr. Yersin | Kupfer-Komplexe für optoelektronische Anwendungen |
| CN103534260A (zh) * | 2011-05-13 | 2014-01-22 | 辛诺拉有限公司 | 铜(i)络合物，尤其用于光电组件 |
-
2011
- 2011-08-26 EP EP11179099A patent/EP2540730A1/de not_active Withdrawn
-
2012
- 2012-06-29 CN CN201280031716.7A patent/CN103748100B/zh active Active
- 2012-06-29 WO PCT/EP2012/062783 patent/WO2013001086A1/de not_active Ceased
- 2012-06-29 JP JP2014517751A patent/JP2014527030A/ja active Pending
- 2012-06-29 EP EP12738418.8A patent/EP2726488B1/de active Active
- 2012-06-29 US US14/129,707 patent/US9917265B2/en active Active
- 2012-06-29 KR KR1020137034502A patent/KR101942324B1/ko active Active
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