CN102084436B - 聚(5，5′-二(噻吩-2-基)苯并[2，1-b；3，4-b′]二噻吩)及其作为高性能可溶液加工半导体聚合物的用途 - Google Patents

聚(5，5′-二(噻吩-2-基)苯并[2，1-b；3，4-b′]二噻吩)及其作为高性能可溶液加工半导体聚合物的用途 Download PDF

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CN102084436B
CN102084436B CN2009801259716A CN200980125971A CN102084436B CN 102084436 B CN102084436 B CN 102084436B CN 2009801259716 A CN2009801259716 A CN 2009801259716A CN 200980125971 A CN200980125971 A CN 200980125971A CN 102084436 B CN102084436 B CN 102084436B
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alkyl
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thin film
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CN102084436A (zh
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M·卡斯特勒
S·克勒
K·米伦
M·刘
D·贝克曼
R·里格尔
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Max Planck Gesellschaft zur Foerderung der Wissenschaften eV
Clap Co Ltd
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BASF SE
Max Planck Gesellschaft zur Foerderung der Wissenschaften eV
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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
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • 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
    • C07D495/04—Ortho-condensed systems
    • 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
    • C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
    • C08G61/126—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one sulfur atom in the ring
    • 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
    • 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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    • H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
    • 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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    • 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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    • 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
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    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
    • 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
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    • Y02E10/549—Organic PV cells

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  • Chemical & Material Sciences (AREA)
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  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Thin Film Transistor (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Photovoltaic Devices (AREA)
CN2009801259716A 2008-07-02 2009-06-25 聚(5，5′-二(噻吩-2-基)苯并[2，1-b；3，4-b′]二噻吩)及其作为高性能可溶液加工半导体聚合物的用途 Expired - Fee Related CN102084436B (zh)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
EP08159524.1 2008-07-02
EP08159524 2008-07-02
EP09153369 2009-02-20
EP09153369.5 2009-02-20
PCT/EP2009/057984 WO2010000669A1 (en) 2008-07-02 2009-06-25 Poly(5,5'bis(thiophen-2-yl)-benzo[2,1-b;3,4-b']dithiophene) and its use as high performance solution processable semiconducting polymer

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CN102084436A CN102084436A (zh) 2011-06-01
CN102084436B true CN102084436B (zh) 2012-10-17

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US (1) US8598304B2 (https=)
EP (1) EP2297748B1 (https=)
JP (1) JP5735418B2 (https=)
KR (1) KR101561323B1 (https=)
CN (1) CN102084436B (https=)
TW (1) TWI476225B (https=)
WO (1) WO2010000669A1 (https=)

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WO2010149451A1 (en) 2009-06-05 2010-12-29 Basf Se Fused bithiophene-vinylene polymers
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US9573158B2 (en) 2014-01-03 2017-02-21 The Regents Of The University Of California High mobility polymer thin-film transistors with capillarity-mediated self-assembly
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US9881712B2 (en) * 2012-07-20 2018-01-30 Rohm And Haas Electronic Materials Llc Highly crystalline electrically conducting polymers, methods of manufacture thereof and articles comprising the same
CN103664994A (zh) * 2012-08-31 2014-03-26 昆山维信诺显示技术有限公司 苯并二噻吩类衍生物有机电致发光材料及其应用
US10128441B2 (en) 2012-09-07 2018-11-13 The Regents Of The University Of California Field-effect transistors based on macroscopically oriented polymers
US9559306B2 (en) 2012-09-07 2017-01-31 The Regents Of The University Of California Field-effect transistors based on macroscopically oriented polymers with high saturation mobility
CN103848969B (zh) * 2012-11-28 2016-03-30 海洋王照明科技股份有限公司 一种含噻唑并噻唑-二苯并噻吩苯并二噻吩聚合物及其制备与应用
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EP2297748A1 (en) 2011-03-23
CN102084436A (zh) 2011-06-01
JP2011526631A (ja) 2011-10-13
EP2297748B1 (en) 2017-01-04
KR101561323B1 (ko) 2015-10-16
TW201008978A (en) 2010-03-01
JP5735418B2 (ja) 2015-06-17
TWI476225B (zh) 2015-03-11
US8598304B2 (en) 2013-12-03
US20110168264A1 (en) 2011-07-14
KR20110043631A (ko) 2011-04-27
WO2010000669A1 (en) 2010-01-07

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