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首页> 外文期刊>ChemPlusChem >Glycolated Thiophene‐Tetrafluorophenylene Copolymers for Bioelectronic Applications: Synthesis by Direct Heteroarylation Polymerisation
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Glycolated Thiophene‐Tetrafluorophenylene Copolymers for Bioelectronic Applications: Synthesis by Direct Heteroarylation Polymerisation

机译:用于生物电子应用的乙二醇噻吩 - 四氟苯基共聚物:通过直接杂芳基化聚合合成

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摘要

Abstract A series of copolymers containing a glycolated 1,4‐dithienyl‐2,3,5,6‐tetrafluorophenylene unit copolymerized with thiophene, bithiophene, thienothiophene and 1,2,4,5‐tetrafluorobenzene comonomer units were designed and synthesised by direct heteroarylation polymerisation. The optical, electrochemical, electrochromic and solid‐state structural properties of the copolymers were investigated. The copolymers exhibit stable redox properties in organic solvents and promising redox properties in thin film configuration with an aqueous electrolyte. Finally, the potential of the copolymers as active materials in organic electrochemical transistors (OECTs) was assessed, and promising performance was shown as an accumulation‐mode OECT material with a peak transconductance of 0.17 mS and a good on/off ratio of 10 5 for the thiophene copolymer.
机译:摘要通过直接杂芳基化设计和合成了含有与噻吩,硫代苯丙基烯,噻吩和1,2,5-四氟苯甲酸二苯甲酸乙二醇烯和1,2,5-四氟苯甲酸乙二醇烯和1,2,5,6-四氟苯基烯烯烯组合的一系列共聚物。 聚合。 研究了共聚物的光学,电化学,电致变色和固态结构性能。 共聚物在有机溶剂中表现出稳定的氧化还原性能,并在具有含水电解质的薄膜构型中有前途的氧化还原性能。 最后,评估作为有机电化学晶体管(OET)中的活性材料的共聚物的电位,并且有希望的性能作为积累 - 模式OET材料,其峰跨导0.17ms,良好的开/关比为10 5 噻吩共聚物。

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  • 来源
    《ChemPlusChem》 |2019年第9期|共7页
  • 作者单位

    Materials Research Institute and School of Biological and Chemical SciencesQueen Mary University of;

    Materials Research Institute and School of Biological and Chemical SciencesQueen Mary University of;

    Materials Research Institute and School of Biological and Chemical SciencesQueen Mary University of;

    Department of Biomedical EngineeringNorthwestern University EvanstonIL 60208 USA;

    Materials Research Centre Faculty of ChemistryBrno University of TechnologyPurkyňova 118 612 00;

    Materials Research Centre Faculty of ChemistryBrno University of TechnologyPurkyňova 118 612 00;

    Department of Biomedical EngineeringNorthwestern University EvanstonIL 60208 USA;

    Materials Research Centre Faculty of ChemistryBrno University of TechnologyPurkyňova 118 612 00;

    Materials Research Institute and School of Biological and Chemical SciencesQueen Mary University of;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

    direct heteroarylation; organic electrochemical transistors; polymerisation; semiconductors; thiophenes;

    机译:直接杂芳基;有机电化学晶体管;聚合;半导体;噻吩;

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