KR101535696B1 - 릴렌-(π-억셉터) 공중합체로부터 제조된 반도체 재료 - Google Patents
릴렌-(π-억셉터) 공중합체로부터 제조된 반도체 재료 Download PDFInfo
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- KR101535696B1 KR101535696B1 KR1020107018818A KR20107018818A KR101535696B1 KR 101535696 B1 KR101535696 B1 KR 101535696B1 KR 1020107018818 A KR1020107018818 A KR 1020107018818A KR 20107018818 A KR20107018818 A KR 20107018818A KR 101535696 B1 KR101535696 B1 KR 101535696B1
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- 0 CC(CCCC(C)CC1C(N2*)=O)CCC1C2=O Chemical compound CC(CCCC(C)CC1C(N2*)=O)CCC1C2=O 0.000 description 6
- DMDHMKZIUNKSBF-AATRIKPKSA-N C/C(/C#N)=C(/C)\C#N Chemical compound C/C(/C#N)=C(/C)\C#N DMDHMKZIUNKSBF-AATRIKPKSA-N 0.000 description 1
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- H—ELECTRICITY
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/10—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aromatic carbon atoms, e.g. polyphenylenes
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- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
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- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
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- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
- C09B69/101—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds containing an anthracene dye
- C09B69/102—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds containing an anthracene dye containing a perylene dye
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- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
- C09B69/105—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds containing a methine or polymethine dye
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- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
- C09B69/106—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds containing an azo dye
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- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/124—Intrinsically conductive polymers
- H01B1/127—Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
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- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
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- H—ELECTRICITY
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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
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/40—Organosilicon compounds, e.g. TIPS pentacene
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
- C09K2211/1458—Heterocyclic containing sulfur as the only heteroatom
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- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
- C09K2211/1483—Heterocyclic containing nitrogen and sulfur as heteroatoms
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/40—Organic transistors
- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/464—Lateral top-gate IGFETs comprising only a single gate
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/40—Organic transistors
- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/466—Lateral bottom-gate IGFETs comprising only a single gate
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/621—Aromatic anhydride or imide compounds, e.g. perylene tetra-carboxylic dianhydride or perylene tetracarboxylic di-imide
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Thin Film Transistor (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Photovoltaic Devices (AREA)
- Electroluminescent Light Sources (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2631108P | 2008-02-05 | 2008-02-05 | |
| US2632208P | 2008-02-05 | 2008-02-05 | |
| US61/026,322 | 2008-02-05 | ||
| US61/026,311 | 2008-02-05 | ||
| US5001008P | 2008-05-02 | 2008-05-02 | |
| US61/050,010 | 2008-05-02 | ||
| US8823608P | 2008-08-12 | 2008-08-12 | |
| US8821508P | 2008-08-12 | 2008-08-12 | |
| US8824608P | 2008-08-12 | 2008-08-12 | |
| US61/088,246 | 2008-08-12 | ||
| US61/088,215 | 2008-08-12 | ||
| US61/088,236 | 2008-08-12 | ||
| US11247808P | 2008-11-07 | 2008-11-07 | |
| US61/112,478 | 2008-11-07 | ||
| PCT/EP2009/051315 WO2009098254A1 (en) | 2008-02-05 | 2009-02-05 | SEMICONDUCTOR MATERIALS PREPARED FROM RYLENE-(π-ACCEPTOR) COPOLYMERS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20100120168A KR20100120168A (ko) | 2010-11-12 |
| KR101535696B1 true KR101535696B1 (ko) | 2015-07-09 |
Family
ID=40590011
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107018818A Active KR101535696B1 (ko) | 2008-02-05 | 2009-02-05 | 릴렌-(π-억셉터) 공중합체로부터 제조된 반도체 재료 |
| KR1020107018815A Withdrawn KR20100115773A (ko) | 2008-02-05 | 2009-02-05 | 페릴렌-이미드 반도체 중합체 |
| KR1020107019216A Active KR101529358B1 (ko) | 2008-02-05 | 2009-02-05 | 나프탈렌-이미드 반도체 중합체 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107018815A Withdrawn KR20100115773A (ko) | 2008-02-05 | 2009-02-05 | 페릴렌-이미드 반도체 중합체 |
| KR1020107019216A Active KR101529358B1 (ko) | 2008-02-05 | 2009-02-05 | 나프탈렌-이미드 반도체 중합체 |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US8470961B2 (enExample) |
| EP (3) | EP2240528B1 (enExample) |
| JP (4) | JP2011515505A (enExample) |
| KR (3) | KR101535696B1 (enExample) |
| CN (3) | CN101939351A (enExample) |
| CA (3) | CA2711764A1 (enExample) |
| TW (3) | TWI408154B (enExample) |
| WO (3) | WO2009098253A1 (enExample) |
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|---|---|---|---|---|
| GB0618955D0 (en) * | 2006-09-26 | 2006-11-08 | Cryscade Solar Ltd | Organic compound and organic photovoltaic device |
| US9000423B2 (en) * | 2007-10-31 | 2015-04-07 | The Regents Of The University Of California | Processing additive for single-component solution processed organic field-effect transistors |
| EP2240528B1 (en) * | 2008-02-05 | 2017-04-12 | Basf Se | Semiconductor materials prepared from rylene-( -acceptor) copolymers |
| WO2009144205A1 (en) * | 2008-05-30 | 2009-12-03 | Basf Se | Rylene-based semiconductor materials and methods of preparation and use thereof |
| TW201026740A (en) * | 2008-11-07 | 2010-07-16 | Basf Se | Organic semiconducting polymers |
| CN102224611B (zh) | 2008-11-24 | 2014-01-22 | 巴斯夫欧洲公司 | 可光固化聚合物电介质及其制备方法和用途 |
| US9221944B2 (en) | 2008-12-18 | 2015-12-29 | Basf Se | Semiconductor materials prepared from dithienylvinylene copolymers |
| US8927971B2 (en) * | 2009-04-06 | 2015-01-06 | University Of Kentucky Research Foundation | Semiconducting compounds and devices incorporating same |
| KR20120005536A (ko) | 2009-04-28 | 2012-01-16 | 바스프 에스이 | 반전도성 층을 제조하는 방법 |
| US8831073B2 (en) * | 2009-08-31 | 2014-09-09 | Sony Corporation | Wireless transmission system, wireless communication device, and wireless communication method |
| US8164089B2 (en) * | 2009-10-08 | 2012-04-24 | Xerox Corporation | Electronic device |
| US8580384B2 (en) | 2010-01-17 | 2013-11-12 | Polyera Corporation | Dielectric materials and methods of preparation and use thereof |
| CN102146151B (zh) * | 2010-02-04 | 2013-10-16 | 海洋王照明科技股份有限公司 | 苝四羧酸二酰亚胺共轭聚合物及其制备方法和应用 |
| WO2011113195A1 (zh) * | 2010-03-15 | 2011-09-22 | 海洋王照明科技股份有限公司 | 有机太阳能电池及其制备方法 |
| JP5477577B2 (ja) * | 2010-03-31 | 2014-04-23 | 凸版印刷株式会社 | ブロック共重合体、有機薄膜、光電変換素子及び太陽電池 |
| US20110266529A1 (en) | 2010-04-27 | 2011-11-03 | The Trustees Of Princeton University | Remote doping of organic thin film transistors |
| US20130085249A1 (en) * | 2010-06-09 | 2013-04-04 | Ocean's King Lighting Science &Technology Co., Ltd | Conjugated polymer based on perylene tetracarboxylic acid diimide and dibenzothiophene and the preparation method and application thereof |
| CN102372840B (zh) * | 2010-08-11 | 2013-04-17 | 海洋王照明科技股份有限公司 | 一类苝四羧酸二酰亚胺共聚物及其制备方法和应用 |
| EP2615097B1 (en) * | 2010-09-10 | 2015-03-04 | Ocean's King Lighting Science&Technology Co., Ltd. | Perylenetetracarboxylic acid diimide organic semiconductive material, preparation method and use thereof |
| RU2595698C2 (ru) * | 2010-09-28 | 2016-08-27 | Конинклейке Филипс Электроникс, Н.В. | Светоизлучающее устройство с органическим люминофором |
| CN103403903B (zh) * | 2010-10-07 | 2017-02-15 | 乔治亚州技术研究公司 | 场效应晶体管及其制造方法 |
| WO2012090110A1 (en) * | 2010-12-30 | 2012-07-05 | Basf Se | Perylene-based semiconductors and methods of preparation and use thereof |
| EP2697236A1 (en) | 2011-04-15 | 2014-02-19 | Georgia Tech Research Corporation | Stannyl derivatives of naphthalene diimides and related compositions and methods |
| US8986842B2 (en) | 2011-05-24 | 2015-03-24 | Ecole Polytechnique Federale De Lausanne (Epfl) | Color conversion films comprising polymer-substituted organic fluorescent dyes |
| JP2014525949A (ja) * | 2011-07-05 | 2014-10-02 | ビーエーエスエフ ソシエタス・ヨーロピア | ジチエノフタルイミド半導体ポリマー |
| FR2980040B1 (fr) * | 2011-09-14 | 2016-02-05 | Commissariat Energie Atomique | Transistor organique a effet de champ |
| CN103044660A (zh) * | 2011-10-11 | 2013-04-17 | 中国科学院化学研究所 | 芳酰亚胺共轭聚合物、其制备方法及其在有机光电子器件中的应用 |
| CN103044661A (zh) * | 2011-10-11 | 2013-04-17 | 中国科学院化学研究所 | 芳酰亚胺共轭聚合物、其制备方法及其在有机光电子器件中的应用 |
| WO2013096924A1 (en) | 2011-12-22 | 2013-06-27 | Georgia Tech Research Corporation | Oligomers and polymers and polymers and methods derived from stannyl derivatives of naphthalene diimides |
| EP2794609A4 (en) * | 2011-12-22 | 2015-05-20 | Chinese Acad Inst Chemistry | REACTION PRODUCTS OF STANNYL DERIVATIVES FROM NAPHTHALINDIIMIDES WITH RYLENE COMPOUNDS |
| WO2013096915A1 (en) | 2011-12-22 | 2013-06-27 | Georgia Tech Research Corporation | Stannyl derivatives of naphthalene diimides and related compositions and methods |
| JP5875709B2 (ja) * | 2012-02-02 | 2016-03-02 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 有機半導体デバイスの製造方法 |
| US10005879B2 (en) * | 2012-02-03 | 2018-06-26 | Basf Se | Method for producing an organic semiconductor device |
| TWI561611B (en) * | 2012-02-04 | 2016-12-11 | Basf Se | Method for producing an organic semiconductor device |
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| US8835598B2 (en) * | 2012-03-22 | 2014-09-16 | Polyera Corporation | Conjugated polymers and their use in optoelectronic devices |
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| EP2808373A1 (en) * | 2013-05-29 | 2014-12-03 | Solvay SA | Semiconductor materials on the basis of rylene diimide derivatives or napththalene derivatives, and polymers and semiconductor devices comprising said materials |
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