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Facile method towards functionalization of partially fluorinated polyarylethers via sequential post-polymerization modification

机译:通过顺序的后聚合修饰实现部分氟化聚芳基醚官能化的简便方法

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摘要

A novel partially fluorinated arylene vinylene ether (FAVE) polymer containing ester groups was synthesized, which was used to prepare three reactive FAVE polymers containing carboxylic acid groups, alcohol groups, and acid chloride groups, respectively. Post-polymerization modifications of the FAVE polymer's carboxylic acid groups (via a DCC coupling procedure with the desired alcohol), alcohol groups (via DCC coupling or an acid chloride esterification procedure with the desired carboxylic acid or acid chloride), and acid chloride groups (via an optimized nucleophilic substitution reaction with the desired alcohol or amine) were successfully performed. Several examples have been successfully prepared to demonstrate the versatility of these developed modification methods. FAVE polymers have been prepared with NHS active ester groups, Disperse Red 1 chromophores, benzyl bromide groups, aryl trifluorovinyl ether groups, ATRP initiator groups, vinyl groups, propargyl groups, Disperse Orange 3 chromophores, and benzaldehyde groups. In most cases, analytical data are consistent with a quantitative conversion of the reactive or functional groups. It is demonstrated that no degradation of the FAVE polymer matrix occurs after multistep post-polymerization modification reactions. Published by Elsevier B.V.
机译:合成了一种新型的含酯基的部分氟化亚芳基亚乙烯基醚(FAVE)聚合物,该聚合物用于制备三种分别含有羧酸基,醇基和酰氯基的反应性FAVE聚合物。 FAVE聚合物的羧酸基团(通过与所需醇的DCC偶联步骤),醇基团(通过DCC偶联或与所需羧酸或酰氯的酰基氯酯化步骤)的后聚合修饰(通过优化的亲核取代反应,与所需的醇或胺成功进行。已成功准备了几个示例,以证明这些开发的修改方法的多功能性。制备了具有NHS活性酯基团,分散红1发色团,苄基溴化物基团,芳基三氟乙烯基醚基团,ATRP引发剂基团,乙烯基,炔丙基,分散橙3发色团和苯甲醛基团的FAVE聚合物。在大多数情况下,分析数据与反应性或官​​能团的定量转化一致。已经证明,在多步后聚合改性反应之后,FAVE聚合物基质没有降解。由Elsevier B.V.发布

著录项

  • 来源
    《Reactive & Functional Polymers》 |2015年第8期|38-46|共9页
  • 作者单位

    Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA|Univ Texas Dallas, Alan G MacDiarmid NanoTech Inst, Richardson, TX 75080 USA;

    Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA|Univ Texas Dallas, Alan G MacDiarmid NanoTech Inst, Richardson, TX 75080 USA;

    Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA|Univ Texas Dallas, Alan G MacDiarmid NanoTech Inst, Richardson, TX 75080 USA;

    Princeton Univ, Princeton, NJ 08544 USA;

    Greenhill Sch, Addison, TX 75001 USA;

    Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA|Univ Texas Dallas, Alan G MacDiarmid NanoTech Inst, Richardson, TX 75080 USA;

    US Air Force Acad, Dept Chem, Colorado Springs, CO 80840 USA|US Air Force Acad, Chem Res Ctr, Colorado Springs, CO 80840 USA;

    Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA|Univ Texas Dallas, Alan G MacDiarmid NanoTech Inst, Richardson, TX 75080 USA;

    Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA|Univ Texas Dallas, Alan G MacDiarmid NanoTech Inst, Richardson, TX 75080 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Fluoropolymers; Post-functionalization; Polymer synthesis; Thermoplastic; Advanced materials;

    机译:含氟聚合物;后功能化;聚合物合成;热塑性;先进材料;

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