JP6284531B2 - 有機電子材料のための構成単位としての有利に製造されたナフタレン誘導体およびペリレン誘導体ならびに染料 - Google Patents
有機電子材料のための構成単位としての有利に製造されたナフタレン誘導体およびペリレン誘導体ならびに染料 Download PDFInfo
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- JP6284531B2 JP6284531B2 JP2015529176A JP2015529176A JP6284531B2 JP 6284531 B2 JP6284531 B2 JP 6284531B2 JP 2015529176 A JP2015529176 A JP 2015529176A JP 2015529176 A JP2015529176 A JP 2015529176A JP 6284531 B2 JP6284531 B2 JP 6284531B2
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- alkyl
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- 0 *c(c1c2c(C(O3)=O)ccc1*)ccc2C3=O Chemical compound *c(c1c2c(C(O3)=O)ccc1*)ccc2C3=O 0.000 description 5
- GGWKVZRAOSOSLQ-UHFFFAOYSA-N Brc(c1c(cc2[s]c3c4)Br)cc([s]c(cc5Br)c67)c6c1c2c3c7c5c4Br Chemical compound Brc(c1c(cc2[s]c3c4)Br)cc([s]c(cc5Br)c67)c6c1c2c3c7c5c4Br GGWKVZRAOSOSLQ-UHFFFAOYSA-N 0.000 description 1
- XUTOCVOZQJYXKP-UHFFFAOYSA-N CC(C)(C)CC(C)(C)c(cc1)ccc1Oc(cc(c1c(cc2Oc3ccc(C(C)(C)CC(C)(C)C)cc3)Br)Br)c(-c3c(cc4Br)Oc5ccc(C(C)(C)CC(C)(C)C)cc5)c1c2-c(c(Oc1ccc(C(C)(C)CC(C)(C)C)cc1)c1)c3c4c1Br Chemical compound CC(C)(C)CC(C)(C)c(cc1)ccc1Oc(cc(c1c(cc2Oc3ccc(C(C)(C)CC(C)(C)C)cc3)Br)Br)c(-c3c(cc4Br)Oc5ccc(C(C)(C)CC(C)(C)C)cc5)c1c2-c(c(Oc1ccc(C(C)(C)CC(C)(C)C)cc1)c1)c3c4c1Br XUTOCVOZQJYXKP-UHFFFAOYSA-N 0.000 description 1
- QCLDKZGJEBOAIJ-UHFFFAOYSA-N CC(C)(C)CC(C)(C)c(cc1)ccc1Oc(cc1C(OC2=O)=O)c(-c(c3c(c(C(OC4=O)=O)c5)c4c4)c5Oc5ccc(C(C)(C)CC(C)(C)C)cc5)c5c1c2cc(Oc1ccc(C(C)(C)CC(C)(C)C)cc1)c5-c3c4Oc1ccc(C(C)(C)CC(C)(C)C)cc1 Chemical compound CC(C)(C)CC(C)(C)c(cc1)ccc1Oc(cc1C(OC2=O)=O)c(-c(c3c(c(C(OC4=O)=O)c5)c4c4)c5Oc5ccc(C(C)(C)CC(C)(C)C)cc5)c5c1c2cc(Oc1ccc(C(C)(C)CC(C)(C)C)cc1)c5-c3c4Oc1ccc(C(C)(C)CC(C)(C)C)cc1 QCLDKZGJEBOAIJ-UHFFFAOYSA-N 0.000 description 1
- MQHFIPBNYMCUCD-UHFFFAOYSA-N CC(c(c1c2cc3[s]c4c5)cc([s]c(cc6C(O7)=O)c89)c8c1c3c4c9c6c5C7=O)(O)OC2=O Chemical compound CC(c(c1c2cc3[s]c4c5)cc([s]c(cc6C(O7)=O)c89)c8c1c3c4c9c6c5C7=O)(O)OC2=O MQHFIPBNYMCUCD-UHFFFAOYSA-N 0.000 description 1
- YDENUNAJNDQYOX-UHFFFAOYSA-N Cc1ccc(C)c2c1c(C(O)=O)ccc2C(O)=O Chemical compound Cc1ccc(C)c2c1c(C(O)=O)ccc2C(O)=O YDENUNAJNDQYOX-UHFFFAOYSA-N 0.000 description 1
- NVXPVSGHKVMXRI-UHFFFAOYSA-N Clc(cc(c1c23)SSc1cc(Cl)c2-c(c1c(c(SS2)c4)c2c2)c2Cl)c3-c1c4Cl Chemical compound Clc(cc(c1c23)SSc1cc(Cl)c2-c(c1c(c(SS2)c4)c2c2)c2Cl)c3-c1c4Cl NVXPVSGHKVMXRI-UHFFFAOYSA-N 0.000 description 1
- KLQCSTWNKAOVGZ-UHFFFAOYSA-N Clc(cc1Br)c(-c(c2c(c(Br)c3)c(Br)c4)c3Cl)c3c1c(Br)cc(Cl)c3-c2c4Cl Chemical compound Clc(cc1Br)c(-c(c2c(c(Br)c3)c(Br)c4)c3Cl)c3c1c(Br)cc(Cl)c3-c2c4Cl KLQCSTWNKAOVGZ-UHFFFAOYSA-N 0.000 description 1
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- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
- C07C25/22—Polycyclic aromatic halogenated hydrocarbons with condensed rings
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- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/06—Peri-condensed systems
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- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
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- C07C211/39—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton
- C07C211/41—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton containing condensed ring systems
- C07C211/42—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton containing condensed ring systems with six-membered aromatic rings being part of the condensed ring systems
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- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/52—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of six-membered aromatic rings being part of condensed ring systems
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- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/22—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of halogens; by substitution of halogen atoms by other halogen atoms
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- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/29—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing halogen
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- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/753—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of polycyclic acids
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
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- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/14—Perylene derivatives
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- C09B3/20—Preparation from starting materials already containing the perylene nucleus by halogenation
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- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/022—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position not provided for in one of the sub groups C09B5/04 - C09B5/20
- C09B5/026—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position not provided for in one of the sub groups C09B5/04 - C09B5/20 only S-containing hetero rings
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
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- H10K85/623—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing five rings, e.g. pentacene
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- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
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- C07C2603/52—Ortho- or ortho- and peri-condensed systems containing five condensed rings
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261694783P | 2012-08-30 | 2012-08-30 | |
| EP12182331.4 | 2012-08-30 | ||
| EP12182331 | 2012-08-30 | ||
| US61/694,783 | 2012-08-30 | ||
| PCT/IB2013/058009 WO2014033622A2 (en) | 2012-08-30 | 2013-08-27 | Conveniently prepared naphthalene and perylene derivatives as building blocks for organic electronic materials and dyestuff |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015534542A JP2015534542A (ja) | 2015-12-03 |
| JP2015534542A5 JP2015534542A5 (enExample) | 2016-12-22 |
| JP6284531B2 true JP6284531B2 (ja) | 2018-02-28 |
Family
ID=46939531
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015529176A Expired - Fee Related JP6284531B2 (ja) | 2012-08-30 | 2013-08-27 | 有機電子材料のための構成単位としての有利に製造されたナフタレン誘導体およびペリレン誘導体ならびに染料 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9382264B2 (enExample) |
| EP (1) | EP2890668B1 (enExample) |
| JP (1) | JP6284531B2 (enExample) |
| KR (1) | KR101764512B1 (enExample) |
| CN (1) | CN104583161B (enExample) |
| WO (1) | WO2014033622A2 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9385326B2 (en) | 2013-01-15 | 2016-07-05 | Basf Se | Triangulene oligomers and polymers and their use as hole conducting material |
| KR20150133785A (ko) | 2013-03-18 | 2015-11-30 | 바스프 에스이 | 페릴렌모노이미드 및 나프탈렌모노이미드 유도체 및 염료-감응성 태양 전지에서 이의 용도 |
| RU2016148230A (ru) * | 2014-05-09 | 2018-06-13 | Басф Се | Цианированные периленовые соединения |
| KR101867399B1 (ko) * | 2015-08-26 | 2018-06-21 | 욱성화학주식회사 | 페릴렌계 화합물, 이의 제조 방법, 및 이를 포함하는 형광 염료 |
| KR102403983B1 (ko) * | 2017-03-31 | 2022-05-30 | 도레이첨단소재 주식회사 | 고색재현 필름, 이의 제조방법 및 이를 포함하는 백라이트 유닛 |
| CN112119515A (zh) | 2018-03-07 | 2020-12-22 | Clap有限公司 | 用于制造顶栅底接触有机场效应晶体管的图案化方法 |
| JP7075682B2 (ja) | 2018-03-08 | 2022-05-26 | クラップ カンパニー リミテッド | 半導電性単層カーボンナノチューブ及び有機半導電性材料を含む有機電界効果トランジスタ |
| EP3735430B1 (en) | 2018-06-26 | 2023-09-13 | Clap Co., Ltd. | Vinylether-based polymer as dielectric |
| JP2020083982A (ja) * | 2018-11-21 | 2020-06-04 | 住友化学株式会社 | 着色硬化性樹脂組成物、カラーフィルタ、表示装置及び化合物 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE340091C (de) | 1921-09-02 | Francois Louis Brodu | Aufspannvorrichtung mit Kugellagerung zwischen Ober- und Unterteil | |
| DE66611C (de) | Badische Anilin- und Sodafabrik in Ludwigshafen a. Rh | Verfahren zur Darstellung eines beizenziehenden Farbstoffs aus Perchlornaphtalin | ||
| DE498039C (de) | 1924-12-19 | 1930-05-17 | Felice Bensa | Verfahren zur Herstellung von Halogensubstitutionsprodukten des Perylens und des 3,10-Perylenchinons |
| DE1154799B (de) | 1962-04-19 | 1963-09-26 | Hoechst Ag | Verfahren zur Herstellung von 4, 5-Dichlor- und 4, 5-Dibrom-naphthalin-1, 8-dicarbonsaeureanhydrid |
| US3652637A (en) | 1968-11-22 | 1972-03-28 | Diamond Shamrock Corp | Vapor phase synthesis of chlorinated aromatic nitriles |
| US4505858A (en) | 1982-10-12 | 1985-03-19 | Ciba-Geigy Corporation | Process for producing 3,4,9,10-tetrathioperylene and 3,4,9,10-tetraselenoperylene |
| DE3400991A1 (de) * | 1984-01-13 | 1985-07-18 | Basf Ag, 6700 Ludwigshafen | Verfahren zum flaechenmaessigen konzentrieren von licht und neue farbstoffe |
| DE3413418A1 (de) * | 1984-04-10 | 1985-10-17 | Basf Ag, 6700 Ludwigshafen | Farbstofflaser |
| FR2627179B1 (fr) * | 1988-02-12 | 1990-06-08 | Thomson Csf | Procede d'obtention de perylenes polyalkyles, perylenes obtenus par ce procede et materiaux organiques a proprietes rpe en derivant |
| DE4316378A1 (de) * | 1993-05-17 | 1994-11-24 | Max Planck Gesellschaft | Perylenderivate |
| US5989737A (en) * | 1997-02-27 | 1999-11-23 | Xerox Corporation | Organic electroluminescent devices |
| US6329084B1 (en) * | 1998-06-15 | 2001-12-11 | Toyo Ink Mfg. Co., Ltd. | Compound for organic electro-luminescence device and organic electro-luminescence device using the compound |
| JP2002003833A (ja) | 2000-06-23 | 2002-01-09 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子用発光材料およびそれを使用した有機エレクトロルミネッセンス素子 |
| JP2002012861A (ja) * | 2000-07-03 | 2002-01-15 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子用発光材料およびそれを使用した有機エレクトロルミネッセンス素子 |
| CN1271168C (zh) * | 2000-09-07 | 2006-08-23 | 出光兴产株式会社 | 有机电场发光元件 |
| JP2003012612A (ja) * | 2001-06-29 | 2003-01-15 | Toyo Ink Mfg Co Ltd | ペリレンの製造方法 |
| JP5538941B2 (ja) * | 2010-02-18 | 2014-07-02 | Jsr株式会社 | レジスト下層膜形成方法、パターン形成方法、および組成物、レジスト下層膜形成材料用添加剤、架橋剤並びにレジスト下層膜 |
| US9056822B2 (en) * | 2011-06-10 | 2015-06-16 | National University Corporation Nagoya University | Method for producing polycyclic aromatic compound substituted by aryl group |
-
2013
- 2013-08-27 CN CN201380044965.4A patent/CN104583161B/zh not_active Expired - Fee Related
- 2013-08-27 EP EP13833442.0A patent/EP2890668B1/en not_active Not-in-force
- 2013-08-27 JP JP2015529176A patent/JP6284531B2/ja not_active Expired - Fee Related
- 2013-08-27 KR KR1020157007594A patent/KR101764512B1/ko not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| CN104583161B (zh) | 2016-12-14 |
| WO2014033622A3 (en) | 2014-04-24 |
| EP2890668A2 (en) | 2015-07-08 |
| EP2890668A4 (en) | 2016-09-07 |
| WO2014033622A2 (en) | 2014-03-06 |
| CN104583161A (zh) | 2015-04-29 |
| US9382264B2 (en) | 2016-07-05 |
| KR101764512B1 (ko) | 2017-08-02 |
| EP2890668B1 (en) | 2019-08-21 |
| JP2015534542A (ja) | 2015-12-03 |
| US20150225418A1 (en) | 2015-08-13 |
| KR20150045515A (ko) | 2015-04-28 |
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