JP2007527420A5 - - Google Patents
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- Publication number
- JP2007527420A5 JP2007527420A5 JP2006554292A JP2006554292A JP2007527420A5 JP 2007527420 A5 JP2007527420 A5 JP 2007527420A5 JP 2006554292 A JP2006554292 A JP 2006554292A JP 2006554292 A JP2006554292 A JP 2006554292A JP 2007527420 A5 JP2007527420 A5 JP 2007527420A5
- Authority
- JP
- Japan
- Prior art keywords
- aryl
- fluoroaryl
- substituted
- fluorine atoms
- heteroaryl
- 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 description 85
- 150000001875 compounds Chemical class 0.000 claims description 65
- 125000001153 fluoro group Chemical group F* 0.000 claims description 56
- 125000004407 fluoroaryl group Chemical group 0.000 claims description 52
- 125000001072 heteroaryl group Chemical group 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 35
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 29
- 125000003545 alkoxy group Chemical group 0.000 claims description 19
- 125000004104 aryloxy group Chemical group 0.000 claims description 18
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 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 16
- 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 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- 229910052731 fluorine Inorganic materials 0.000 claims description 14
- 125000006574 non-aromatic ring group Chemical group 0.000 claims description 14
- 125000001424 substituent group Chemical group 0.000 claims description 14
- 125000001769 aryl amino group Chemical group 0.000 claims description 10
- 125000005504 styryl group Chemical group 0.000 claims description 10
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical group [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 229940114081 cinnamate Drugs 0.000 claims description 6
- 235000019000 fluorine Nutrition 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000004429 atom Chemical group 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 2
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical group C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 claims description 2
- -1 fluoroalkyl Compound Chemical class 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 0 CC(*)(*)c1ccccc1 Chemical compound CC(*)(*)c1ccccc1 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- TUXUJVDBDXGHMS-UHFFFAOYSA-N 3-[4-(n-phenylanilino)phenyl]prop-2-enoic acid Chemical compound C1=CC(C=CC(=O)O)=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 TUXUJVDBDXGHMS-UHFFFAOYSA-N 0.000 description 1
- CEHJRVLXQNQKLH-UHFFFAOYSA-N 3-[4-(n-phenylanilino)phenyl]prop-2-enoyl chloride Chemical compound C1=CC(C=CC(=O)Cl)=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 CEHJRVLXQNQKLH-UHFFFAOYSA-N 0.000 description 1
- MCHJEWAZSNQQMN-UHFFFAOYSA-N C1C=CC(c2ccccc2)=CC1 Chemical compound C1C=CC(c2ccccc2)=CC1 MCHJEWAZSNQQMN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/783,304 US7365230B2 (en) | 2004-02-20 | 2004-02-20 | Cross-linkable polymers and electronic devices made with such polymers |
| PCT/US2005/005584 WO2005083034A1 (en) | 2004-02-20 | 2005-02-17 | Aromatic amine compositions comprising and electronic devices made with such compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007527420A JP2007527420A (ja) | 2007-09-27 |
| JP2007527420A5 true JP2007527420A5 (https=) | 2008-04-03 |
Family
ID=34861198
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006554292A Pending JP2007527420A (ja) | 2004-02-20 | 2005-02-17 | 芳香族アミン組成物包含、およびそのような組成物で製造された電子デバイス |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7365230B2 (https=) |
| EP (2) | EP1723214B1 (https=) |
| JP (1) | JP2007527420A (https=) |
| KR (1) | KR101135745B1 (https=) |
| TW (1) | TWI372780B (https=) |
| WO (1) | WO2005083034A1 (https=) |
Families Citing this family (124)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2499364A1 (en) | 2002-09-24 | 2004-04-08 | E. I. Du Pont De Nemours And Company | Water dispersible polyanilines made with polymeric acid colloids for electronics applications |
| JP4464277B2 (ja) * | 2002-09-24 | 2010-05-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性有機ポリマー／ナノ粒子複合材料およびその使用方法 |
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| KR20060133056A (ko) * | 2004-03-31 | 2006-12-22 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 전하 수송 물질용 트리아릴아민 화합물 |
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| US7960587B2 (en) | 2004-02-19 | 2011-06-14 | E.I. Du Pont De Nemours And Company | Compositions comprising novel compounds and electronic devices made with such compositions |
| US7365230B2 (en) | 2004-02-20 | 2008-04-29 | E.I. Du Pont De Nemours And Company | Cross-linkable polymers and electronic devices made with such polymers |
| JP4407536B2 (ja) | 2004-03-01 | 2010-02-03 | 三菱化学株式会社 | アリールアミン系化合物、並びにそれを用いた電子写真感光体及び画像形成装置 |
| JP4956885B2 (ja) | 2004-03-10 | 2012-06-20 | 富士ゼロックス株式会社 | 有機電界発光素子 |
| KR20060133056A (ko) | 2004-03-31 | 2006-12-22 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 전하 수송 물질용 트리아릴아민 화합물 |
-
2004
- 2004-02-20 US US10/783,304 patent/US7365230B2/en not_active Expired - Lifetime
-
2005
- 2005-02-17 WO PCT/US2005/005584 patent/WO2005083034A1/en not_active Ceased
- 2005-02-17 KR KR1020067019221A patent/KR101135745B1/ko not_active Expired - Fee Related
- 2005-02-17 EP EP05723475A patent/EP1723214B1/en not_active Expired - Lifetime
- 2005-02-17 EP EP10010702.8A patent/EP2261299B1/en not_active Expired - Lifetime
- 2005-02-17 JP JP2006554292A patent/JP2007527420A/ja active Pending
- 2005-02-18 TW TW094104928A patent/TWI372780B/zh not_active IP Right Cessation
-
2007
- 2007-12-28 US US11/966,123 patent/US8716697B2/en not_active Expired - Fee Related
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