JP2013506984A5 - - Google Patents
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- JP2013506984A5 JP2013506984A5 JP2012531434A JP2012531434A JP2013506984A5 JP 2013506984 A5 JP2013506984 A5 JP 2013506984A5 JP 2012531434 A JP2012531434 A JP 2012531434A JP 2012531434 A JP2012531434 A JP 2012531434A JP 2013506984 A5 JP2013506984 A5 JP 2013506984A5
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- JP
- Japan
- Prior art keywords
- electronic device
- matrix material
- organic
- anion
- salt
- 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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- 150000001450 anions Chemical class 0.000 claims description 10
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000002891 organic anions Chemical class 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- HCAUQPZEWLULFJ-UHFFFAOYSA-N benzo[f]quinoline Chemical group C1=CC=C2C3=CC=CC=C3C=CC2=N1 HCAUQPZEWLULFJ-UHFFFAOYSA-N 0.000 claims description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 claims description 2
- WGDRAVMHLDKGGA-UHFFFAOYSA-N prop-2-en-1-imine Chemical group [CH2]C=C[NH] WGDRAVMHLDKGGA-UHFFFAOYSA-N 0.000 claims description 2
- 125000006413 ring segment Chemical group 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 10
- -1 phosphate anion Chemical class 0.000 claims 9
- 150000001768 cations Chemical class 0.000 claims 7
- 229910052751 metal Inorganic materials 0.000 claims 6
- 239000002184 metal Substances 0.000 claims 6
- 229910019142 PO4 Inorganic materials 0.000 claims 3
- 239000002019 doping agent Substances 0.000 claims 3
- 239000010452 phosphate Substances 0.000 claims 3
- 238000000034 method Methods 0.000 claims 2
- 150000003967 siloles Chemical class 0.000 claims 2
- 239000000758 substrate Substances 0.000 claims 2
- XNCMQRWVMWLODV-UHFFFAOYSA-N 1-phenylbenzimidazole Chemical compound C1=NC2=CC=CC=C2N1C1=CC=CC=C1 XNCMQRWVMWLODV-UHFFFAOYSA-N 0.000 claims 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 claims 1
- XESMNQMWRSEIET-UHFFFAOYSA-N 2,9-dinaphthalen-2-yl-4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC(C=2C=C3C=CC=CC3=CC=2)=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=C(C=3C=C4C=CC=CC4=CC=3)N=C21 XESMNQMWRSEIET-UHFFFAOYSA-N 0.000 claims 1
- CELPGKFEUDCZOU-UHFFFAOYSA-N 2-naphthalen-2-yl-4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=C(C=3C=C4C=CC=CC4=CC=3)N=C21 CELPGKFEUDCZOU-UHFFFAOYSA-N 0.000 claims 1
- ZVFQEOPUXVPSLB-UHFFFAOYSA-N 3-(4-tert-butylphenyl)-4-phenyl-5-(4-phenylphenyl)-1,2,4-triazole Chemical compound C1=CC(C(C)(C)C)=CC=C1C(N1C=2C=CC=CC=2)=NN=C1C1=CC=C(C=2C=CC=CC=2)C=C1 ZVFQEOPUXVPSLB-UHFFFAOYSA-N 0.000 claims 1
- BSVILDUORGWESI-UHFFFAOYSA-N 3-methyl-2-(4-naphthalen-2-ylphenyl)imidazo[4,5-f][1,10]phenanthroline Chemical compound C1=CC=CC2=CC(C3=CC=C(C=C3)C=3N(C4=C(C5=CC=CN=C5C5=NC=CC=C54)N=3)C)=CC=C21 BSVILDUORGWESI-UHFFFAOYSA-N 0.000 claims 1
- DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 claims 1
- AOQKGYRILLEVJV-UHFFFAOYSA-N 4-naphthalen-1-yl-3,5-diphenyl-1,2,4-triazole Chemical compound C1=CC=CC=C1C(N1C=2C3=CC=CC=C3C=CC=2)=NN=C1C1=CC=CC=C1 AOQKGYRILLEVJV-UHFFFAOYSA-N 0.000 claims 1
- RFVBBELSDAVRHM-UHFFFAOYSA-N 9,10-dinaphthalen-2-yl-2-phenylanthracene Chemical compound C1=CC=CC=C1C1=CC=C(C(C=2C=C3C=CC=CC3=CC=2)=C2C(C=CC=C2)=C2C=3C=C4C=CC=CC4=CC=3)C2=C1 RFVBBELSDAVRHM-UHFFFAOYSA-N 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- XZCJVWCMJYNSQO-UHFFFAOYSA-N butyl pbd Chemical compound C1=CC(C(C)(C)C)=CC=C1C1=NN=C(C=2C=CC(=CC=2)C=2C=CC=CC=2)O1 XZCJVWCMJYNSQO-UHFFFAOYSA-N 0.000 claims 1
- 238000010549 co-Evaporation Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- RFDGVZHLJCKEPT-UHFFFAOYSA-N tris(2,4,6-trimethyl-3-pyridin-3-ylphenyl)borane Chemical compound CC1=C(B(C=2C(=C(C=3C=NC=CC=3)C(C)=CC=2C)C)C=2C(=C(C=3C=NC=CC=3)C(C)=CC=2C)C)C(C)=CC(C)=C1C1=CC=CN=C1 RFDGVZHLJCKEPT-UHFFFAOYSA-N 0.000 claims 1
- 238000007740 vapor deposition Methods 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910004283 SiO 4 Inorganic materials 0.000 description 1
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 1
- NKVMCSDLYHGDMD-UHFFFAOYSA-N methanetetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)(C(O)=O)C(O)=O NKVMCSDLYHGDMD-UHFFFAOYSA-N 0.000 description 1
- RKGQUTNLMXNUME-UHFFFAOYSA-N methanetricarboxylic acid Chemical compound OC(=O)C(C(O)=O)C(O)=O RKGQUTNLMXNUME-UHFFFAOYSA-N 0.000 description 1
- MZYHMUONCNKCHE-UHFFFAOYSA-N naphthalene-1,2,3,4-tetracarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=C(C(O)=O)C(C(O)=O)=C21 MZYHMUONCNKCHE-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009047880A DE102009047880A1 (de) | 2009-09-30 | 2009-09-30 | Organische elektronische Vorrichtung und Verfahren zu dessen Herstellung |
| DE102009047880.9 | 2009-09-30 | ||
| PCT/EP2010/064592 WO2011039323A2 (de) | 2009-09-30 | 2010-09-30 | Organische elektronische vorrichtung und verfahren zu dessen herstellung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013506984A JP2013506984A (ja) | 2013-02-28 |
| JP2013506984A5 true JP2013506984A5 (OSRAM) | 2013-07-25 |
| JP5757951B2 JP5757951B2 (ja) | 2015-08-05 |
Family
ID=43085757
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012531434A Expired - Fee Related JP5757951B2 (ja) | 2009-09-30 | 2010-09-30 | 有機電子装置およびその製造方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9520570B2 (OSRAM) |
| EP (1) | EP2483945B1 (OSRAM) |
| JP (1) | JP5757951B2 (OSRAM) |
| KR (1) | KR101770437B1 (OSRAM) |
| CN (1) | CN102576823B (OSRAM) |
| DE (1) | DE102009047880A1 (OSRAM) |
| WO (1) | WO2011039323A2 (OSRAM) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2524913B1 (en) | 2010-01-15 | 2017-07-26 | Idemitsu Kosan Co., Ltd. | Nitrogenated heterocyclic ring derivative and organic electroluminescent element comprising same |
| DE102012211869A1 (de) | 2012-07-06 | 2014-01-09 | Osram Opto Semiconductors Gmbh | Organisches Licht emittierendes Bauelement |
| DE102012217574A1 (de) * | 2012-09-27 | 2014-03-27 | Siemens Aktiengesellschaft | Phosphoroxo-Salze als n-Dotierstoffe für die organische Elektronik |
| DE102013106949A1 (de) | 2013-07-02 | 2015-01-08 | Osram Opto Semiconductors Gmbh | Optoelektronisches Bauelement, organische funktionelle Schicht und Verfahren zur Herstellung eines optoelektronischen Bauelements |
| EP2960315A1 (de) | 2014-06-27 | 2015-12-30 | cynora GmbH | Organische Elektrolumineszenzvorrichtung |
| CN106715644B (zh) | 2014-09-17 | 2020-08-18 | 辛诺拉有限公司 | 用作为发射体的有机分子 |
| DE102015210388A1 (de) | 2015-06-05 | 2016-12-08 | Siemens Aktiengesellschaft | Organische Heterozyklische Alkalimetallsalze als n-Dotierstoffe in der Organischen Elektronik |
| EP3312896B1 (en) * | 2016-10-24 | 2021-03-31 | Novaled GmbH | Organic electroluminescent device comprising a redox-doped electron transport layer and an auxiliary electron transport layer |
| JP2019026619A (ja) * | 2017-08-03 | 2019-02-21 | 国立大学法人山形大学 | ターピリジン誘導体、及びそれを用いた有機電子素子 |
| CN109994651B (zh) * | 2017-12-29 | 2020-12-25 | 昆山国显光电有限公司 | 一种有机电致发光器件及其制备方法 |
| KR102291411B1 (ko) * | 2019-12-09 | 2021-08-23 | 엘티소재주식회사 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
| US20210336151A1 (en) * | 2020-04-28 | 2021-10-28 | Semiconductor Energy Laboratory Co., Ltd. | Light-Emitting Device Material, Electron-Transport Layer Material, Organic Compound, Light-Emitting Device, Light-Emitting Apparatus, Electronic Device, and Lighting Device |
| CN112194614B (zh) * | 2020-10-14 | 2022-04-26 | 新乡医学院 | 一种特异性识别Fe3+的三联吡啶荧光探针及其合成方法和应用 |
| CN114695799A (zh) * | 2020-12-29 | 2022-07-01 | 常州强力昱镭光电材料有限公司 | 一种有机电致发光元件 |
| CN112903331B (zh) * | 2021-02-25 | 2022-07-29 | 北京空间飞行器总体设计部 | 一种水升华器供水压力地面等效模拟装置及方法 |
| CN116982407A (zh) * | 2021-03-26 | 2023-10-31 | 东丽株式会社 | 有机el显示装置及其制造方法 |
| CN115207228B (zh) * | 2021-04-08 | 2025-06-03 | 常州强力电子新材料股份有限公司 | 有机电致发光元件 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6064151A (en) * | 1997-12-08 | 2000-05-16 | Motorola, Inc. | Organic electroluminescent device with enhanced performance |
| JP2004193011A (ja) * | 2002-12-12 | 2004-07-08 | Fuji Photo Film Co Ltd | 有機電界発光素子 |
| JP4366106B2 (ja) * | 2003-04-30 | 2009-11-18 | キヤノン株式会社 | 発光素子 |
| US7608855B2 (en) | 2004-04-02 | 2009-10-27 | Spansion Llc | Polymer dielectrics for memory element array interconnect |
| US7622200B2 (en) * | 2004-05-21 | 2009-11-24 | Semiconductor Energy Laboratory Co., Ltd. | Light emitting element |
| JP4988152B2 (ja) * | 2004-08-03 | 2012-08-01 | 株式会社Ａｄｅｋａ | 蛍光性陰イオンおよび蛍光性陽イオンからなる塩 |
| JP2007226043A (ja) | 2006-02-24 | 2007-09-06 | Mitsubishi Paper Mills Ltd | 酸化亜鉛膜の形成方法及び透明導電性基材 |
| DE102006053644A1 (de) | 2006-11-14 | 2008-06-12 | Siemens Ag | Neuartiges hochleitfähiges organisches Ladungsträgertransportmaterial |
| JP5656338B2 (ja) | 2007-03-12 | 2015-01-21 | ケミプロ化成株式会社 | 新規な１，１０−フェナントロリン誘導体、電子輸送材料、電子注入材料およびそれを含有する有機電界発光素子 |
| JP5008584B2 (ja) * | 2008-02-15 | 2012-08-22 | 富士フイルム株式会社 | 有機電界発光素子及び表示装置 |
| JP5515234B2 (ja) * | 2008-03-31 | 2014-06-11 | 住友化学株式会社 | 中間層形成塗布液、および有機エレクトロルミネッセンス素子の製造方法、並びに有機エレクトロルミネッセンス素子 |
-
2009
- 2009-09-30 DE DE102009047880A patent/DE102009047880A1/de not_active Withdrawn
-
2010
- 2010-09-30 WO PCT/EP2010/064592 patent/WO2011039323A2/de not_active Ceased
- 2010-09-30 EP EP10759683.5A patent/EP2483945B1/de active Active
- 2010-09-30 US US13/499,542 patent/US9520570B2/en active Active
- 2010-09-30 CN CN201080044055.2A patent/CN102576823B/zh active Active
- 2010-09-30 JP JP2012531434A patent/JP5757951B2/ja not_active Expired - Fee Related
- 2010-09-30 KR KR1020127010788A patent/KR101770437B1/ko not_active Expired - Fee Related
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