JP2008214307A5 - - Google Patents
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- Publication number
- JP2008214307A5 JP2008214307A5 JP2007057025A JP2007057025A JP2008214307A5 JP 2008214307 A5 JP2008214307 A5 JP 2008214307A5 JP 2007057025 A JP2007057025 A JP 2007057025A JP 2007057025 A JP2007057025 A JP 2007057025A JP 2008214307 A5 JP2008214307 A5 JP 2008214307A5
- Authority
- JP
- Japan
- Prior art keywords
- represented
- formula
- group
- formulas
- naphthyl
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims description 35
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- 239000001257 hydrogen Substances 0.000 claims description 33
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
- 125000001424 substituent group Chemical group 0.000 claims description 14
- -1 phosphoryl groups Chemical group 0.000 claims description 13
- 125000004429 atom Chemical group 0.000 claims description 12
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 10
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000005647 linker group Chemical group 0.000 claims description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims 17
- 125000001624 naphthyl group Chemical group 0.000 claims 6
- 239000001963 growth medium Substances 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- MWVTWFVJZLCBMC-UHFFFAOYSA-N 4,4'-bipyridine Chemical group C1=NC=CC(C=2C=CN=CC=2)=C1 MWVTWFVJZLCBMC-UHFFFAOYSA-N 0.000 claims 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 230000005525 hole transport Effects 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Chemical group 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 0 Cc1cnc(C)[n]1* Chemical compound Cc1cnc(C)[n]1* 0.000 description 3
- AUQXBLORTHZXQD-UHFFFAOYSA-N CC1OC(C)=CN1 Chemical compound CC1OC(C)=CN1 AUQXBLORTHZXQD-UHFFFAOYSA-N 0.000 description 1
- WAPSEVALXZJQLL-UHFFFAOYSA-N Cc(c1c2)cccc1cc1c2c(C)ccc1 Chemical compound Cc(c1c2)cccc1cc1c2c(C)ccc1 WAPSEVALXZJQLL-UHFFFAOYSA-N 0.000 description 1
- QHMBTFDCPDJYOU-UHFFFAOYSA-N Cc(cc1)cc2c1[n](C)c1c2cc(C)cc1 Chemical compound Cc(cc1)cc2c1[n](C)c1c2cc(C)cc1 QHMBTFDCPDJYOU-UHFFFAOYSA-N 0.000 description 1
- ZDCMUYGSDXNSOR-UHFFFAOYSA-N Cc(cc1)cc2c1c1ccccc1c1ccc(C)cc21 Chemical compound Cc(cc1)cc2c1c1ccccc1c1ccc(C)cc21 ZDCMUYGSDXNSOR-UHFFFAOYSA-N 0.000 description 1
- CUWOOCLTSZMQOL-UHFFFAOYSA-N Cc(cc1)ccc1-[n]1c(cc(C)cc2)c2c2c1cc(C)cc2 Chemical compound Cc(cc1)ccc1-[n]1c(cc(C)cc2)c2c2c1cc(C)cc2 CUWOOCLTSZMQOL-UHFFFAOYSA-N 0.000 description 1
- WVUHHPQQQLBMOE-UHFFFAOYSA-N Cc1cnc(C)[s]1 Chemical compound Cc1cnc(C)[s]1 WVUHHPQQQLBMOE-UHFFFAOYSA-N 0.000 description 1
- LCZUOKDVTBMCMX-UHFFFAOYSA-N Cc1ncc(C)nc1 Chemical compound Cc1ncc(C)nc1 LCZUOKDVTBMCMX-UHFFFAOYSA-N 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007057025A JP5176343B2 (ja) | 2007-03-07 | 2007-03-07 | 電子輸送材料およびこれを用いた有機電界発光素子 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007057025A JP5176343B2 (ja) | 2007-03-07 | 2007-03-07 | 電子輸送材料およびこれを用いた有機電界発光素子 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008214307A JP2008214307A (ja) | 2008-09-18 |
| JP2008214307A5 true JP2008214307A5 (enExample) | 2010-04-15 |
| JP5176343B2 JP5176343B2 (ja) | 2013-04-03 |
Family
ID=39834780
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007057025A Active JP5176343B2 (ja) | 2007-03-07 | 2007-03-07 | 電子輸送材料およびこれを用いた有機電界発光素子 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5176343B2 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH1144632A (ja) * | 1997-07-28 | 1999-02-16 | Toa Medical Electronics Co Ltd | 粒子計測装置のデータ異常判定方法 |
| JP5722036B2 (ja) | 2007-08-08 | 2015-05-20 | ユニバーサル ディスプレイ コーポレイション | リン光発光ダイオード中の単一トリフェニレン発色団 |
| US8062771B2 (en) * | 2009-02-03 | 2011-11-22 | Nitto Denko Corporation | Ambipolar host in organic light emitting diode |
| JP5594286B2 (ja) * | 2009-03-26 | 2014-09-24 | 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の製造方法、および有機エレクトロルミネッセンス素子 |
| WO2010132538A1 (en) * | 2009-05-12 | 2010-11-18 | Schering Corporation | Fused tricyclic aryl compounds useful for the treatment of viral diseases |
| TW201134812A (en) | 2010-02-10 | 2011-10-16 | Sensient Imaging Technologies | Bipyridyl substituted derivates of anthracene and their use in organic electroluminescence devices |
| JP5549270B2 (ja) * | 2010-02-19 | 2014-07-16 | Ｊｎｃ株式会社 | アントラセン誘導体およびこれを用いた有機電界発光素子 |
| CN102439004A (zh) | 2010-04-20 | 2012-05-02 | 出光兴产株式会社 | 双咔唑衍生物、有机电致发光元件用材料及使用其的有机电致发光元件 |
| WO2012037269A1 (en) | 2010-09-16 | 2012-03-22 | Nitto Denko Corporation | Substituted bipyridines for use in organic light-emitting devices |
| CN102442938A (zh) * | 2010-10-12 | 2012-05-09 | 清华大学 | 一种并二芴类化合物及其应用 |
| CN102532105A (zh) * | 2010-12-17 | 2012-07-04 | 清华大学 | 一种含有吡啶基团的三亚苯类化合物及其应用 |
| US9705091B2 (en) | 2010-12-20 | 2017-07-11 | Idemitsu Kosan Co., Ltd. | Aromatic heterocycle derivative and organic electroluminescent element using same |
| EP2679581B1 (en) | 2011-02-23 | 2017-08-09 | Hodogaya Chemical Co., Ltd. | Compound containing substituted triphenyle ring structure, and organic electroluminescent element |
| US9328094B2 (en) | 2011-09-19 | 2016-05-03 | Nitto Denko Corporation | Substituted biaryl compounds for light-emitting devices |
| JP6126577B2 (ja) * | 2012-02-28 | 2017-05-10 | 保土谷化学工業株式会社 | 置換基を有するピリジル基とトリフェニレン環構造を有する化合物および有機エレクトロルミネッセンス素子 |
| CN104379572B (zh) * | 2012-06-28 | 2016-09-21 | 捷恩智株式会社 | 苯并[a]咔唑化合物、电子输送材料及使用其的有机电场发光元件 |
| CN103022376B (zh) * | 2012-12-06 | 2015-08-12 | 昆山维信诺显示技术有限公司 | 一种oled器件 |
| JP6448369B2 (ja) | 2014-02-03 | 2019-01-09 | キヤノン株式会社 | 有機発光素子 |
| KR102263057B1 (ko) | 2014-05-07 | 2021-06-09 | 삼성전자주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
| CN109796398A (zh) * | 2019-02-18 | 2019-05-24 | 山西医科大学 | 一种百草枯单吡啶酮碘化物的制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1186605B1 (en) * | 2000-09-07 | 2003-04-16 | Chisso Corporation | Organic electroluminescent device comprising dipyridylthiophene derivative |
| JP4432313B2 (ja) * | 2001-10-10 | 2010-03-17 | 東レ株式会社 | テトラフェニルメタン誘導体、及びこれを含む発光素子 |
| JP4646494B2 (ja) * | 2002-04-11 | 2011-03-09 | 出光興産株式会社 | 新規含窒素複素環誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| EP2385052B1 (en) * | 2004-03-25 | 2013-11-13 | Hodogaya Chemical Co., Ltd. | Compound having oxadiazole ring structure substituted with pyridyl group, and organic electroluminescent device |
| JP2006176491A (ja) * | 2004-11-25 | 2006-07-06 | Kyoto Univ | ピレン系化合物及びこれを用いた発光トランジスタ素子 |
| US20060186797A1 (en) * | 2005-02-15 | 2006-08-24 | Tosoh Corporation | Pi-conjugated compound having cardo structure, process for preparing same and use of same |
-
2007
- 2007-03-07 JP JP2007057025A patent/JP5176343B2/ja active Active
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