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A comparative study of diaryl carbene insertion reactions at polymer surfaces

机译:聚合物表面二芳基卡宾插入反应的比较研究

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摘要

A detailed investigation of the reactions of diaryldiazo compounds for the surface modification of several polymers has been conducted. This has revealed that the rate of reaction of diaryldiazo compounds is influenced by their substituents, that the reaction is exothermic, and that the polymer itself exerts an influence on the surface modification. The results are consistent with the formation and insertion of a carbene intermediate at the polymer surface. It was further shown that such surface modified polymers, characterized using surface sensitive techniques, display macroscopic behavior consistent with the presence of the newly introduced surface chemical functionality, characterized using a combination of surface sensitive and bulk analytical techniques. This approach is complementary to directed energy deposition approaches, offers an alternative route to functional polymers, and provide a direct link between surface chemistry and observable macroscopic properties.
机译:已经详细研究了二芳基重氮化合物对几种聚合物进行表面改性的反应。这表明二芳基重氮化合物的反应速率受其取代基的影响,该反应是放热的,并且聚合物本身对表面改性产生影响。结果与在聚合物表面上卡宾中间体的形成和插入一致。进一步表明,使用表面敏感技术表征的这种表面改性的聚合物表现出与新引入的表面化学官能度的存在一致的宏观行为,所述表面化学官能度使用表面敏感技术和本体分析技术的组合来表征。该方法是定向能量沉积方法的补充,为功能性聚合物提供了另一种途径,并提供了表面化学和可观察到的宏观性能之间的直接联系。

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  • 来源
    《Applied Surface Science》 |2019年第28期|754-762|共9页
  • 作者单位

    Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England;

    Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England;

    Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England;

    Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England;

    Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England;

    Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England;

    Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England;

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  • 正文语种 eng
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  • 入库时间 2022-08-18 04:09:47

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