Synthesis and electrochromism of highly organosoluble polyamides and polyimides with bulky trityl-substituted triphenylamine units

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Abstract

© 2017 by the authors. 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.

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Hsiao, S. H., Liao, W. K., & Liou, G. S. (2017). Synthesis and electrochromism of highly organosoluble polyamides and polyimides with bulky trityl-substituted triphenylamine units. Polymers, 9(10). https://doi.org/10.3390/polym9100511

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