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The synthesis of mesogenic polymers provoked by molecular mobility. Polysiloxanarylenes

机译:分子流动性引起的介晶聚合物的合成。聚硅氧烷

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摘要

An approach to the synthesis of potentially thermotropic liquid crystalline polymers based on parallel investigation of their molecular mobility was realized. The initial idea was provoked by the observation that there exists some correspondence of molecular mobility data and the ability of a polymer to form a liquid crystalline phase. Previously this phenomenon was demonstrated on the example of a series of thermotropic main chain polymers with flexible dimethylsiloxane spacers of variable length. The relation between the structure of the main chain and local molecular mobility of different fragments was investigated in a series of regular polysiloxanesilarylenes containing rigid aromatic sequences. Molecular mobility was studied by dielectric spectroscopy in solution and in solid state. The structure of the main chain has been changed by variation of the repeated fragments' length, substituents and joint groups, The data of molecular mobility and their conformity with the chain structure were used for directed synthetic search of desired mesogenic polymers. [References: 12]
机译:基于对分子迁移率的平行研究,实现了一种潜在的热致液晶聚合物的合成方法。最初的想法是由于观察到分子迁移率数据与聚合物形成液晶相的能力存在某种对应关系而引起的。以前,这种现象在一系列具有可变长度的柔性二甲基硅氧烷间隔基的热主链聚合物的例子中得到了证明。在一系列含有刚性芳族序列的常规聚硅氧烷亚芳基中,研究了主链结构与不同片段的局部分子迁移率之间的关系。通过介电谱在溶液和固态中研究了分子迁移率。通过改变重复片段的长度,取代基和连接基团来改变主链的结构。分子迁移率数据及其与链结构的一致性被用于定向合成所需的介晶聚合物。 [参考:12]

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