CN101939352B - 由萘嵌苯(rylene)-(π-受体)共聚物制备的半导体材料 - Google Patents

由萘嵌苯(rylene)-(π-受体)共聚物制备的半导体材料 Download PDF

Info

Publication number
CN101939352B
CN101939352B CN200980104292.0A CN200980104292A CN101939352B CN 101939352 B CN101939352 B CN 101939352B CN 200980104292 A CN200980104292 A CN 200980104292A CN 101939352 B CN101939352 B CN 101939352B
Authority
CN
China
Prior art keywords
alkyl
polymers
groups
group
occurrence
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.)
Active
Application number
CN200980104292.0A
Other languages
English (en)
Chinese (zh)
Other versions
CN101939352A (zh
Inventor
A·法凯蒂
陈志华
颜河
吕少峰
T·J·马克斯
郑焱
M·卡斯特勒
S·瓦伊迪耶纳森
F·多茨
S·克勒
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Feilisi Co Ltd
Original Assignee
POLYERA CORP
BASF SE
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by POLYERA CORP, BASF SE filed Critical POLYERA CORP
Publication of CN101939352A publication Critical patent/CN101939352A/zh
Application granted granted Critical
Publication of CN101939352B publication Critical patent/CN101939352B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • 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
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C—CHEMISTRY; METALLURGY
    • 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
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • 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
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • 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
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • 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
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • 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
    • C—CHEMISTRY; METALLURGY
    • 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
    • C09K11/00—Luminescent materials, e.g. electroluminescent or chemiluminescent
    • C09K11/06—Luminescent materials, e.g. electroluminescent or chemiluminescent containing organic luminescent materials
    • 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
    • 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 [2D] radiating surfaces
    • H05B33/14—Light sources with substantially two-dimensional [2D] 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
    • 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]
    • 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
    • H10K85/10—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
    • 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
    • H10K85/10—Organic polymers or oligomers
    • H10K85/151—Copolymers
    • 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
    • C—CHEMISTRY; METALLURGY
    • 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
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/12—Copolymers
    • C08G2261/124—Copolymers alternating
    • C—CHEMISTRY; METALLURGY
    • 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
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/14—Side-groups
    • C08G2261/143—Side-chains containing nitrogen
    • C08G2261/1432—Side-chains containing nitrogen containing amide groups
    • C—CHEMISTRY; METALLURGY
    • 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
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
    • C08G2261/3223—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
    • C—CHEMISTRY; METALLURGY
    • 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
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/90—Applications
    • C08G2261/92—TFT applications
    • C—CHEMISTRY; METALLURGY
    • 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
    • C—CHEMISTRY; METALLURGY
    • 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
    • C09K2211/1483—Heterocyclic containing nitrogen and sulfur as heteroatoms
    • 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
    • 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
    • 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
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Thin Film Transistor (AREA)
  • Photovoltaic Devices (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Electroluminescent Light Sources (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
CN200980104292.0A 2008-02-05 2009-02-05 由萘嵌苯(rylene)-(π-受体)共聚物制备的半导体材料 Active CN101939352B (zh)

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
US61/026,311 2008-02-05
US61/026,322 2008-02-05
US5001008P 2008-05-02 2008-05-02
US61/050,010 2008-05-02
US8824608P 2008-08-12 2008-08-12
US8821508P 2008-08-12 2008-08-12
US8823608P 2008-08-12 2008-08-12
US61/088,236 2008-08-12
US61/088,246 2008-08-12
US61/088,215 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
CN101939352A CN101939352A (zh) 2011-01-05
CN101939352B true CN101939352B (zh) 2014-04-16

Family

ID=40590011

Family Applications (3)

Application Number Title Priority Date Filing Date
CN200980104292.0A Active CN101939352B (zh) 2008-02-05 2009-02-05 由萘嵌苯(rylene)-(π-受体)共聚物制备的半导体材料
CN200980108214.8A Active CN101965374B (zh) 2008-02-05 2009-02-05 萘-酰亚胺半导体聚合物
CN2009801042916A Pending CN101939351A (zh) 2008-02-05 2009-02-05 苝酰亚胺半导体聚合物

Family Applications After (2)

Application Number Title Priority Date Filing Date
CN200980108214.8A Active CN101965374B (zh) 2008-02-05 2009-02-05 萘-酰亚胺半导体聚合物
CN2009801042916A Pending CN101939351A (zh) 2008-02-05 2009-02-05 苝酰亚胺半导体聚合物

Country Status (8)

Country Link
US (3) US9219233B2 (2)
EP (3) EP2240528B1 (2)
JP (4) JP5649977B2 (2)
KR (3) KR101535696B1 (2)
CN (3) CN101939352B (2)
CA (3) CA2711764A1 (2)
TW (3) TW200951160A (2)
WO (3) WO2009098250A1 (2)

Families Citing this family (107)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US9219233B2 (en) * 2008-02-05 2015-12-22 Basf Se Semiconductor materials prepared from rylene-(π-acceptor)copolymers
WO2009144205A1 (en) * 2008-05-30 2009-12-03 Basf Se Rylene-based semiconductor materials and methods of preparation and use thereof
US8664339B2 (en) * 2008-11-07 2014-03-04 Polyera Corporation Organic semiconducting polymers
JP5684715B2 (ja) * 2008-11-24 2015-03-18 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ 光硬化性ポリマー性誘電体、及びその製造方法、及びその使用方法
WO2010079064A2 (en) 2008-12-18 2010-07-15 Basf Se Semiconductor materials prepared from dithienylvinylene copolymers
WO2010117449A2 (en) * 2009-04-06 2010-10-14 University Of Kentucky Research Foundation Semiconducting compounds and devices incorporating same
WO2010125011A2 (de) 2009-04-28 2010-11-04 Basf Se Verfahren zur herstellung von halbleitenden schichten
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
WO2011134959A1 (en) 2010-04-27 2011-11-03 University Of Princeton Remote n-doping of organic thin film transistors
CN103025787B (zh) * 2010-06-09 2014-07-23 海洋王照明科技股份有限公司 基于苝四羧酸二酰亚胺和苯并二噻吩的共轭聚合物及其制备方法和应用
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
US8598302B2 (en) * 2010-09-10 2013-12-03 Ocean's King Lighting Science & Technology Co., Ltd. Perylenetetracarboxylic diimide organic semiconductor material and the preparation method and application thereof
US9310050B2 (en) * 2010-09-28 2016-04-12 Koninklijke Philips N.V. Light-emitting arrangement with organic phosphor
WO2012048048A1 (en) * 2010-10-07 2012-04-12 Georgia Tech Research Corporation Field-effect transistor and manufacturing process thereof
JP5734456B2 (ja) * 2010-12-30 2015-06-17 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ ペリレンを基礎とする半導体、並びにそれらの製造及び使用方法
JP2014518551A (ja) 2011-04-15 2014-07-31 ジョージア テック リサーチ コーポレーション 有機半導体としてのナフタレン−ジイミド−複素環−ナフタレンジイミドオリゴマーおよびそれに由来するトランジスタ
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
EP2794609A4 (en) * 2011-12-22 2015-05-20 Chinese Acad Inst Chemistry REACTION PRODUCTS OF STANNYL DERIVATIVES FROM NAPHTHALINDIIMIDES WITH RYLENE COMPOUNDS
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
WO2013096915A1 (en) 2011-12-22 2013-06-27 Georgia Tech Research Corporation Stannyl derivatives of naphthalene diimides and related compositions and methods
KR101607421B1 (ko) 2012-02-02 2016-03-29 바스프 에스이 유기 반도체 장치의 제조 방법
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
TWI589602B (zh) 2012-02-07 2017-07-01 飛利斯有限公司 可光固化聚合材料及相關電子裝置
JP5859872B2 (ja) * 2012-02-17 2016-02-16 富士フイルム株式会社 有機光電変換素子組成物、これを含む薄膜、光電池、これに用いられる有機半導体ポリマー、化合物およびポリマーの製造方法
US8835598B2 (en) * 2012-03-22 2014-09-16 Polyera Corporation Conjugated polymers and their use in optoelectronic devices
CN104508009B (zh) * 2012-05-28 2016-09-07 宇部兴产株式会社 聚酰亚胺前体和聚酰亚胺
KR20150017718A (ko) 2012-05-31 2015-02-17 미쓰비시 가가꾸 가부시키가이샤 코폴리머, 유기 반도체 재료, 유기 전자 디바이스 및 태양 전지 모듈
EP2858099A4 (en) 2012-06-01 2015-05-20 Mitsubishi Chem Corp METHOD FOR PRODUCING A METAL-OXIDE-CONTAINING SEMICONDUCTOR LAYER AND ELECTRONIC DEVICE
US8901547B2 (en) 2012-08-25 2014-12-02 Polyera Corporation Stacked structure organic light-emitting transistors
CN108103057B (zh) 2012-08-28 2021-09-03 阿科尼生物系统公司 用于纯化核酸的方法和试剂盒
CN105051087A (zh) * 2012-12-18 2015-11-11 巴斯夫欧洲公司 基于萘二酰亚胺-亚乙烯基-低聚噻吩-亚乙烯基聚合物的半导体材料
US20140273339A1 (en) * 2013-03-13 2014-09-18 Saudi Basic Industries Corporation Semiconductor Polymers
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
CN105659310B (zh) 2013-08-13 2021-02-26 飞利斯有限公司 电子显示区域的优化
WO2015031501A1 (en) 2013-08-27 2015-03-05 Polyera Corporation Attachable device having a flexible electronic component
WO2015031426A1 (en) 2013-08-27 2015-03-05 Polyera Corporation Flexible display and detection of flex state
CN103739829A (zh) * 2013-09-06 2014-04-23 中国科学院上海有机化学研究所 受体-受体型交替共轭聚合物及其制备方法和应用
WO2015038684A1 (en) 2013-09-10 2015-03-19 Polyera Corporation Attachable article with signaling, split display and messaging features
CN104674348B (zh) * 2013-12-02 2017-05-10 济南大学 一种制备不同晶相的硫化锌/双亲苝酰亚胺混杂半导体材料的方法
EP3087560B9 (en) 2013-12-24 2021-08-11 Flexterra, Inc. Support structures for a flexible electronic component
WO2015100224A1 (en) 2013-12-24 2015-07-02 Polyera Corporation Flexible electronic display with user interface based on sensed movements
KR20160103083A (ko) 2013-12-24 2016-08-31 폴리에라 코퍼레이션 탈부착형 2차원 플렉서블 전자 기기용 지지 구조물
TWI676880B (zh) 2013-12-24 2019-11-11 美商飛利斯有限公司 動態可撓物品
US20150227245A1 (en) 2014-02-10 2015-08-13 Polyera Corporation Attachable Device with Flexible Electronic Display Orientation Detection
US10261634B2 (en) 2014-03-27 2019-04-16 Flexterra, Inc. Infrared touch system for flexible displays
US10672988B2 (en) 2014-04-18 2020-06-02 Massachusetts Institute Of Technology Functionalized nanostructures and devices including photovoltaic devices
WO2015184045A2 (en) 2014-05-28 2015-12-03 Polyera Corporation Device with flexible electronic components on multiple surfaces
WO2015183567A1 (en) 2014-05-28 2015-12-03 Polyera Corporation Low power display updates
EP2960280A1 (en) 2014-06-26 2015-12-30 E.T.C. S.r.l. Photocrosslinkable compositions, patterned high k thin film dielectrics and related devices
WO2016100983A1 (en) 2014-12-19 2016-06-23 Polyera Corporation Photocrosslinkable compositions, patterned high k thin film dielectrics and related devices
WO2016138356A1 (en) 2015-02-26 2016-09-01 Polyera Corporation Attachable device having a flexible electronic component
CN107531637B (zh) * 2015-03-31 2021-10-22 索尼公司 用于在有机光电二极管中的有机光电转换层的n和p活性材料
US10254795B2 (en) 2015-05-06 2019-04-09 Flexterra, Inc. Attachable, flexible display device with flexible tail
CN109996757A (zh) * 2015-06-12 2019-07-09 罗地亚经营管理公司 含枝状体的混合纳米粒子、生产此类混合纳米粒子的方法以及它们的用途
CN104974334B (zh) * 2015-06-19 2018-05-25 南京工业大学 一种有机电子传输材料
WO2017006765A1 (ja) 2015-07-07 2017-01-12 富士フイルム株式会社 有機半導体素子、化合物、有機半導体組成物、および、有機半導体膜の製造方法
JP6484724B2 (ja) 2015-11-20 2019-03-13 富士フイルム株式会社 有機半導体組成物、有機半導体膜、有機薄膜トランジスタおよび有機薄膜トランジスタの製造方法
US10818849B2 (en) * 2015-12-29 2020-10-27 The University Of Chicago Electron acceptors based on alpha-position substituted PDI for OPV solar cells
EP3432375B1 (en) 2016-03-16 2021-12-29 FUJIFILM Corporation Organic semiconductor composition, method for manufacturing organic thin film transistor, and organic thin film transistor
JP2017183153A (ja) * 2016-03-31 2017-10-05 株式会社デンソー 有機ｅｌ素子の製造方法
WO2017170279A1 (ja) 2016-04-01 2017-10-05 富士フイルム株式会社 有機半導体素子、重合体、有機半導体組成物及び有機半導体膜
WO2017170280A1 (ja) 2016-04-01 2017-10-05 富士フイルム株式会社 有機半導体素子、重合体、有機半導体組成物及び有機半導体膜
CN105679940A (zh) * 2016-04-19 2016-06-15 中国科学院化学研究所 一种双极性聚合物场效应晶体管及其制备方法与应用
CN109153772B (zh) 2016-05-25 2022-05-03 Clap有限公司 半导体
CN107523290B (zh) * 2016-06-20 2019-10-18 国家纳米科学中心 一种有机分子二维有序结构及其制备方法
US9831434B1 (en) 2016-06-22 2017-11-28 International Business Machines Corporation Functionalized pyranopyran-derived acceptors for donor-acceptor polymers
CN109478595B (zh) 2016-06-27 2023-02-07 富士胶片株式会社 有机薄膜晶体管、有机半导体膜、化合物、有机薄膜晶体管用组合物及有机薄膜晶体管的制造方法
WO2018021970A1 (en) * 2016-07-25 2018-02-01 Agency For Science, Technology And Research Conjugated polyviologen derivatives
WO2018076247A1 (en) * 2016-10-27 2018-05-03 South University Of Science And Technology Of China A weak electron-donating building block, copolymers thereof and their preparation methods as well as their applications
JP6752466B2 (ja) 2017-03-31 2020-09-09 富士フイルム株式会社 有機半導体素子、有機半導体組成物、有機半導体膜の製造方法、有機半導体膜、並びに、これらに用いる化合物及びポリマー
JP6814448B2 (ja) 2017-03-31 2021-01-20 富士フイルム株式会社 有機半導体素子、有機半導体組成物、有機半導体膜の製造方法、有機半導体膜、並びに、これらに用いる化合物及びポリマー
WO2018181055A1 (ja) 2017-03-31 2018-10-04 富士フイルム株式会社 有機半導体素子、有機半導体組成物、有機半導体膜の製造方法、有機半導体膜、並びに、これらに用いる化合物及びポリマー
CN107286157B (zh) * 2017-06-06 2019-07-23 武汉工程大学 一种苝二酰亚胺类化合物及其制备方法、应用
US10647851B2 (en) * 2017-07-28 2020-05-12 Phillips 66 Company 1,2,5,6-Naphthalenediimide co-polymer
CN107501527A (zh) * 2017-08-01 2017-12-22 南昌大学 一类基于1,8‑萘酰亚胺的高迁移率半导体聚合物及合成方法
CN111032567B (zh) 2017-08-31 2023-05-09 松下知识产权经营株式会社 杂富勒烯以及使用了其的n型半导体膜和电子设备
CN107556461B (zh) * 2017-08-31 2019-12-06 京东方科技集团股份有限公司 聚合物及其制备方法和太阳能电池
JP6547140B1 (ja) 2017-08-31 2019-07-24 パナソニックＩｐマネジメント株式会社 ｐ型半導体膜および電子デバイス
JP6892076B2 (ja) * 2017-08-31 2021-06-18 東洋紡株式会社 ｎ型半導体として使用可能な化合物
CN109749060B (zh) * 2017-11-03 2024-02-20 东莞伏安光电科技有限公司 一种侧链支化点可调的萘酰亚胺n型共轭聚合物及其应用
CN109651631B (zh) * 2018-01-18 2020-09-25 深圳瑞华泰薄膜科技股份有限公司 一种低介质损耗的聚酰亚胺薄膜
US11345778B2 (en) 2018-01-19 2022-05-31 Flexterra, Inc. Organic dielectric materials and devices including them
JP6927504B2 (ja) 2018-01-23 2021-09-01 富士フイルム株式会社 有機半導体素子、有機半導体組成物、有機半導体膜、有機半導体膜の製造方法、及び、これらに用いるポリマー
KR102130593B1 (ko) * 2018-06-07 2020-07-06 한국과학기술연구원 자가치유 광활성층 형성용 조성물 및 이를 포함하는 유기태양전지
CN108727568B (zh) * 2018-06-08 2020-10-16 福建师范大学 可交联的基于萘二酰亚胺的全聚物太阳能电池受体材料、制备方法及其应用
CN108658993B (zh) * 2018-06-25 2020-07-10 兰州大学 一种芘酰亚胺衍生物及其合成方法和应用
KR102338209B1 (ko) * 2019-05-15 2021-12-10 주식회사 엘지화학 유기발광소자용 재료의 선별방법
CN112430239B (zh) * 2019-08-26 2022-03-22 广州华睿光电材料有限公司 基于七元环结构的化合物、高聚物、混合物、组合物及有机电子器件
CN111748342A (zh) * 2020-07-13 2020-10-09 常熟涤纶有限公司 一种可荧光识别的聚丙烯酸高荧光微球及其制备方法
DE102020126207A1 (de) 2020-10-07 2022-04-07 ZF Automotive Safety Germany GmbH Gassackmodulbaugruppe, verfahren zu deren herstellung und qualitätsprüfung sowie fahrzeuglenkrad mit einer solchen gassackmodulbaugruppe
CN113416201B (zh) * 2021-05-10 2022-08-19 复旦大学 p掺杂有机小分子及其制备方法和应用
CN113956447B (zh) * 2021-10-17 2024-04-02 徐州工程学院 基于稠环酰亚胺结构的电子型聚合物及其制备方法和器件应用
JP7565564B2 (ja) * 2021-12-09 2024-10-11 国立大学法人大阪大学 化合物、有機半導体材料、および有機電子デバイス
CN115020625A (zh) * 2022-07-12 2022-09-06 青岛科技大学 一种有机半导体分子纳米层状结构及其制备方法
PL446287A1 (pl) * 2023-10-02 2025-04-07 Politechnika Śląska Polimer perinonowy z rdzeniem perylenowym oraz sposób otrzymywania polimeru perinonowego z rdzeniem perylenowym w procesie polimeryzacji elektrochemicznej

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006117383A1 (de) * 2005-05-04 2006-11-09 Basf Aktiengesellschaft Terrylen- und quaterrylenderivate
WO2007006717A1 (de) * 2005-07-11 2007-01-18 Basf Aktiengesellschaft Substituierte rylenderivate
WO2007093643A1 (de) * 2006-02-17 2007-08-23 Basf Se Fluorierte rylentetracarbonsäurederivate und deren verwendung
EP1843407A1 (de) * 2006-04-07 2007-10-10 Basf Aktiengesellschaft Flüssig-kristalline Rylentetracarbonsäurederivate und deren Verwendung
CN101068790A (zh) * 2004-11-29 2007-11-07 巴斯福股份公司 环氨基取代的萘嵌苯四羧酸二酰亚胺

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05291598A (ja) * 1991-10-30 1993-11-05 Ricoh Co Ltd 有機光起電力素子
DE19848555A1 (de) * 1998-10-21 2000-04-27 Heinz Langhals Neue Fluoreszenzfarbstoffe durch Kern-Erweiterung von Perylen-3,4:9,10-tetracarbonsäurebisimiden
US6585914B2 (en) * 2000-07-24 2003-07-01 Northwestern University N-type thiophene semiconductors
AU2001281343A1 (en) * 2000-07-24 2002-02-05 Northwestern University N-type thiophene semiconductors
JP4053289B2 (ja) * 2001-12-12 2008-02-27 本田技研工業株式会社 蓄電池の温度制御装置、及びそれを用いた車両装置
CN1554726A (zh) * 2003-12-27 2004-12-15 复旦大学 一种电致发光器件用聚合物材料及其制备方法
WO2005076815A2 (en) * 2004-01-26 2005-08-25 Northwestern University PERYLENE n-TYPE SEMICONDUCTORS AND RELATED DEVICES
US7528176B2 (en) * 2004-09-14 2009-05-05 Northwestern University Carbonyl-functionalized thiophene compounds and related device structures
US7198977B2 (en) * 2004-12-21 2007-04-03 Eastman Kodak Company N,N′-di(phenylalky)-substituted perylene-based tetracarboxylic diimide compounds as n-type semiconductor materials for thin film transistors
US7605394B2 (en) * 2004-12-23 2009-10-20 Northwestern University Siloxane-polymer dielectric compositions and related organic field-effect transistors
US7422777B2 (en) * 2005-11-22 2008-09-09 Eastman Kodak Company N,N′-dicycloalkyl-substituted naphthalene-based tetracarboxylic diimide compounds as n-type semiconductor materials for thin film transistors
US7678463B2 (en) * 2005-12-20 2010-03-16 Northwestern University Intercalated superlattice compositions and related methods for modulating dielectric property
EP1997219A4 (en) * 2006-03-09 2009-07-22 Konarka Technologies Inc PHOTOVOLTAIC CELLS
WO2007146250A2 (en) * 2006-06-12 2007-12-21 Northwestern University Naphthalene-based semiconductor materials and methods of preparing and use thereof
WO2008063609A2 (en) 2006-11-17 2008-05-29 Polyera Corporation Diimide-based semiconductor materials and methods of preparing and using the same
US7892454B2 (en) * 2006-11-17 2011-02-22 Polyera Corporation Acene-based organic semiconductor materials and methods of preparing and using the same
KR20090117730A (ko) * 2007-01-08 2009-11-12 폴리에라 코퍼레이션 아렌-비스(디카르복스이미드)-기재 반도체 물질, 및 이를 제조하기 위한 관련된 중간체의 제조 방법
WO2008091670A2 (en) * 2007-01-24 2008-07-31 Polyera Corporation Organic semiconductor materials and precursors thereof
US9219233B2 (en) * 2008-02-05 2015-12-22 Basf Se Semiconductor materials prepared from rylene-(π-acceptor)copolymers

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101068790A (zh) * 2004-11-29 2007-11-07 巴斯福股份公司 环氨基取代的萘嵌苯四羧酸二酰亚胺
WO2006117383A1 (de) * 2005-05-04 2006-11-09 Basf Aktiengesellschaft Terrylen- und quaterrylenderivate
WO2007006717A1 (de) * 2005-07-11 2007-01-18 Basf Aktiengesellschaft Substituierte rylenderivate
WO2007093643A1 (de) * 2006-02-17 2007-08-23 Basf Se Fluorierte rylentetracarbonsäurederivate und deren verwendung
EP1843407A1 (de) * 2006-04-07 2007-10-10 Basf Aktiengesellschaft Flüssig-kristalline Rylentetracarbonsäurederivate und deren Verwendung

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"A hight-mobility electron-transport polymer with broad absorption and its use in field-effect transistors and all-polymer solar cells";ZHAN等;《JOURNAL OF THE AMERICAN CHEMICAL SOCIETY》;20070518;第129卷(第18期);7246-7247 *
"Tuning orbital Energetics in Arylene Diimide Semiconductors,Materials Design for Ambient Stability of n-Typer Charge Trsanport";EBOOKS JONES等;《JOURNAL OF THE AMERICAN CHEMICAL SOCIETY》;20070101;第129卷(第49期);15259-15278 *

Also Published As

Publication number Publication date
WO2009098253A1 (en) 2009-08-13
JP2014237844A (ja) 2014-12-18
JP5649977B2 (ja) 2015-01-07
JP2011514399A (ja) 2011-05-06
TW200951159A (en) 2009-12-16
EP2240529A1 (en) 2010-10-20
CN101965374A (zh) 2011-02-02
CA2711764A1 (en) 2009-08-13
EP2240530A1 (en) 2010-10-20
KR20100120168A (ko) 2010-11-12
JP2011515505A (ja) 2011-05-19
CN101939352A (zh) 2011-01-05
EP2240530B1 (en) 2015-05-20
US20100283047A1 (en) 2010-11-11
CA2713083A1 (en) 2009-08-13
WO2009098253A9 (en) 2009-10-15
WO2009098254A1 (en) 2009-08-13
US9219233B2 (en) 2015-12-22
CN101965374B (zh) 2014-04-16
JP5683274B2 (ja) 2015-03-11
EP2240528B1 (en) 2017-04-12
WO2009098250A1 (en) 2009-08-13
US20100326527A1 (en) 2010-12-30
TW201000512A (en) 2010-01-01
JP2011514913A (ja) 2011-05-12
CA2713852A1 (en) 2009-08-13
EP2240528A1 (en) 2010-10-20
CN101939351A (zh) 2011-01-05
TWI408154B (zh) 2013-09-11
EP2240529B1 (en) 2017-07-19
US8470961B2 (en) 2013-06-25
KR20100115773A (ko) 2010-10-28
US20110120558A1 (en) 2011-05-26
US8796672B2 (en) 2014-08-05
KR101535696B1 (ko) 2015-07-09
KR101529358B1 (ko) 2015-06-16
TW200951160A (en) 2009-12-16
TWI427098B (zh) 2014-02-21
KR20100115786A (ko) 2010-10-28

Similar Documents

Publication Publication Date Title
CN101939352B (zh) 由萘嵌苯(rylene)-(π-受体)共聚物制备的半导体材料
CN102460758B (zh) 半导体化合物和包含该半导体化合物的设备
TWI511997B (zh) 共軛聚合物及其於光電子裝置的用途
CN102893422B (zh) 吡咯并[3,2-b]吡咯半导体化合物及采用该化合物的器件
CN102317345B (zh) 由二噻吩基亚乙烯基共聚物制备的半导体材料
JP5728003B2 (ja) 縮合ビチオフェンビニレンコポリマー
CN103635505B (zh) 二噻吩并邻苯二甲酰亚胺半导体聚合物
CN102906892B (zh) 共轭聚合物及采用该聚合物的器件
CN106795318B (zh) 分子半导体和聚合物半导体及相关器件
US20150194608A1 (en) Building block for low bandgap conjugated polymers
Domínguez Martín et al. Cyclopentadithiophene-based Co-oligomers for Solution-processed Organic Solar Cells

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20170612

Address after: Ludwigshafen, Germany

Co-patentee after: Feilisi Co. Ltd.

Patentee after: BASF SE

Address before: Ludwigshafen, Germany

Co-patentee before: Polyera Corp.

Patentee before: BASF SE

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20190424

Address after: Illinois State

Patentee after: Feilisi Co. Ltd.

Address before: Ludwigshafen, Germany

Co-patentee before: Feilisi Co. Ltd.

Patentee before: BASF SE

TR01 Transfer of patent right