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Synthesis and Electrochromism of Highly Organosoluble Polyamides and Polyimides with Bulky Trityl-Substituted Triphenylamine Units

机译:带有三苯甲基取代的三苯胺单元的高度有机溶解性聚酰胺和聚酰亚胺的合成和电致变色

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摘要

Two series of polyamides and polyimides containing bulky trityl-substituted triphenylamine units were synthesized from condensation reactions of 4,4′-diamino-4′′-trityltriphenylamine with various dicarboxylic acids and tetracarboxylic dianhydrides, respectively. The polymers showed good solubility and film-forming ability. Flexible or robust films could be readily obtained via solution-casting. The use of aliphatic diacid or dianhydride reduces interchain charge transfer complexing and leads to colorless polyamide and polyimide films. These polymers showed glass-transition temperatures in the range of 206–336 °C. Cyclic voltammograms of the polyamide and polyimide films displayed reversible electrochemical oxidation processes in the range of 0–1.0 or 0–1.3 V. Upon oxidation, the color of polymer films changes from colorless to blue-green or blue. As compared to the polyimide counterparts, the polyamides showed lower oxidation potentials and thus a higher electrochromic stability and coloration efficiency. Simple electrochromic devices were also fabricated as a preliminary investigation for electrochromic applications of the prepared polymers.
机译:分别由4,4'-二氨基-4''-三苯甲基三苯胺与各种二羧酸和四羧酸二酐的缩合反应合成了两个含有大量三苯甲基取代的三苯胺单元的聚酰胺和聚酰亚胺。该聚合物显示出良好的溶解性和成膜能力。通过溶液流延可以容易地获得柔性或坚固的膜。脂族二酸或二酐的使用减少了链间电荷转移的络合并导致无色的聚酰胺和聚酰亚胺膜。这些聚合物的玻璃化转变温度为206–336°C。聚酰胺和聚酰亚胺薄膜的循环伏安图显示了在0–1.0或0–1.3 V范围内可逆的电化学氧化过程。氧化后,聚合物薄膜的颜色从无色变为蓝绿色或蓝色。与聚酰亚胺对应物相比,聚酰胺显示出较低的氧化电位,因此具有较高的电致变色稳定性和着色效率。还制备了简单的电致变色器件,作为对制备的聚合物进行电致变色应用的初步研究。

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