BR112015031519A2 - método para preparação de polímeros electrocrômicos baseados em dióxi-heterociclos - Google Patents

método para preparação de polímeros electrocrômicos baseados em dióxi-heterociclos

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Publication number
BR112015031519A2
BR112015031519A2 BR112015031519A BR112015031519A BR112015031519A2 BR 112015031519 A2 BR112015031519 A2 BR 112015031519A2 BR 112015031519 A BR112015031519 A BR 112015031519A BR 112015031519 A BR112015031519 A BR 112015031519A BR 112015031519 A2 BR112015031519 A2 BR 112015031519A2
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Brazil
Prior art keywords
polymerization
preparing
dhap
monomers
substituted
Prior art date
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BR112015031519A
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English (en)
Inventor
Antonio Arroyave-Mondragon Frank
Deininger James
R Reynolds John
ESTRADA Leandro
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Georgia Tech Res Inst
Univ Florida
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Application filed by Georgia Tech Res Inst, Univ Florida filed Critical Georgia Tech Res Inst
Publication of BR112015031519A2 publication Critical patent/BR112015031519A2/pt

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    • C08G75/00Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/02Polythioethers
    • C08G75/06Polythioethers from cyclic thioethers
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    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123Macromolecular 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
    • C08G61/126Macromolecular 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/32Polythiazoles; Polythiadiazoles
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K9/00Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
    • C09K9/02Organic tenebrescent materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
    • H01B1/124Intrinsically conductive polymers
    • H01B1/127Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
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    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10Definition of the polymer structure
    • C08G2261/14Side-groups
    • C08G2261/141Side-chains having aliphatic units
    • C08G2261/1412Saturated aliphatic units
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    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10Definition of the polymer structure
    • C08G2261/14Side-groups
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    • C08G2261/1424Side-chains containing oxygen containing ether groups, including alkoxy
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    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/322Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
    • C08G2261/3223Monomer 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
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    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/324Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain condensed
    • C08G2261/3243Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain condensed containing one or more sulfur atoms as the only heteroatom, e.g. benzothiophene
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    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/40Polymerisation processes
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    • C08G2261/50Physical properties
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    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
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    • C09K2211/1441Heterocyclic
    • C09K2211/1491Heterocyclic containing other combinations of heteroatoms
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

a presente invenção refere-se a um método para preparação de um polímero conjugado que envolve a polimerização de dhap de um 3,4-dioxitiofeno, 3,4-dioxifurano, ou 3,4-dioxipirrola e, opcionalmente, pelo menos um segundo monômero conjugado na presença de um catalisador incluindo pd ou ni, um solvente aprótico, e um ácido carboxílico a uma temperatura em excesso de 120ºc. pelo menos um dos monômeros é substituído com funcionalidades reativas com hidrogênio e pelo menos um dos monômeros é substituído com um cl, br e/ou i. a polimerização pode ser realizada a uma temperatura de 140ºc ou mais, e a polimerização de dhap pode ser realizada sem um ligante de fosfina ou um agente de transferência de fase. o polímero resultante pode apresentar uma dispersividade menor que 2 e possuir um grau de polimerização em excesso de 10.
BR112015031519A 2013-06-18 2014-06-18 método para preparação de polímeros electrocrômicos baseados em dióxi-heterociclos BR112015031519A2 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361836206P 2013-06-18 2013-06-18
PCT/US2014/042844 WO2014205024A1 (en) 2013-06-18 2014-06-18 Method for preparing dioxyheterocycle-based electrochromic polymers

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BR112015031519A2 true BR112015031519A2 (pt) 2017-07-25

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US (1) US9790326B2 (pt)
EP (1) EP3010959B1 (pt)
JP (1) JP6449865B2 (pt)
KR (1) KR20160023788A (pt)
CN (1) CN105473641A (pt)
AU (1) AU2014281580A1 (pt)
BR (1) BR112015031519A2 (pt)
CA (1) CA2915381C (pt)
IL (1) IL243062B (pt)
MX (1) MX2015017659A (pt)
RU (1) RU2016101074A (pt)
SG (1) SG11201510277YA (pt)
WO (1) WO2014205024A1 (pt)

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US10294326B2 (en) 2014-05-23 2019-05-21 University Of Florida Research Foundation, Incorporated Broadly absorbing electrochromic polymers
TWI516520B (zh) * 2014-10-31 2016-01-11 財團法人工業技術研究院 波長轉換聚合物、其製法及包含其之波長轉換裝置
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CN105576125B (zh) * 2016-02-04 2018-06-29 南京邮电大学 一种用于离子检测的有机场效应晶体管及其检测方法
CN105679939A (zh) * 2016-03-15 2016-06-15 南京邮电大学 一种基于掺杂噻吩异靛的有机薄膜场效应晶体管及其制备方法
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CN111158167A (zh) * 2020-02-14 2020-05-15 南京宜凯瑞新材料有限公司 可调光变色眼镜
CN111349216B (zh) * 2020-02-14 2023-02-03 南京宜凯瑞新材料有限公司 一种电致变色聚合物及用于大规模纯化电致变色聚合物的方法
CN111171293A (zh) * 2020-02-15 2020-05-19 南京宜凯瑞新材料有限公司 绿色至透明电致变色聚合物及其制备方法
CN111187397B (zh) * 2020-02-15 2023-02-24 南京宜凯瑞新材料有限公司 紫色至透明电致变色聚合物及其制备方法
CN112574397A (zh) * 2021-01-12 2021-03-30 长春工业大学 一类可绿色溶剂加工电致变色共轭聚合物制备及应用
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CN105473641A (zh) 2016-04-06
KR20160023788A (ko) 2016-03-03
IL243062B (en) 2019-09-26
CA2915381C (en) 2021-04-27
JP6449865B2 (ja) 2019-01-09
EP3010959A1 (en) 2016-04-27
WO2014205024A1 (en) 2014-12-24
SG11201510277YA (en) 2016-01-28
AU2014281580A1 (en) 2016-01-21
JP2016523298A (ja) 2016-08-08
US20160122476A1 (en) 2016-05-05
MX2015017659A (es) 2016-08-08
AU2014281580A8 (en) 2016-02-11
CA2915381A1 (en) 2014-12-24
US9790326B2 (en) 2017-10-17
EP3010959B1 (en) 2021-04-21
EP3010959A4 (en) 2017-03-08
RU2016101074A (ru) 2017-07-21

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