Synthesis and electrochromic properties of triphenylamine containing copolymers: Effect of π‐bridge on electrochemical properties |
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Authors: | Serife O. Hacioglu Sinem Toksabay Merve Sendur Levent Toppare |
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Affiliation: | 1. Department of Chemistry, Middle East Technical University, , 06800 Ankara, Turkey;2. Institut für Physikalische und Theoretische Chemie, Universit?t Regensburg, , 93053 Regensburg, Germany;3. Department of Biotechnology, Middle East Technical University, , 06800 Ankara, Turkey;4. Department of Polymer Science and Technology, Middle East Technical University, , 06800 Ankara, Turkey;5. The Center for Solar Energy Research and Application (GüNAM), Middle East Technical University, , 06800 Ankara, Turkey |
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Abstract: | In this study, a series of benzotriazole (BTz) and triphenylamine (TPA)‐based random copolymers; poly4‐(5‐(2‐dodecyl‐7‐methyl‐2H‐benzo[d][1,2,3]triazol‐4‐yl)thiophen‐2‐yl)‐N‐(4‐(5‐methylthiophen‐2‐yl)phenyl)‐N‐phenylaniline ( P1 ), poly4′‐(2‐dodecyl‐7‐methyl‐2H‐benzo[d][1,2,3]triazol‐4‐yl)‐N‐(4′‐methyl‐[1,1′‐biphenyl]‐4‐yl)‐N‐phenyl‐[1,1′‐biphenyl]‐4‐amine ( P2 ), and poly4‐(5′‐(2‐dodecyl‐7‐(5‐methylthiophen‐2‐yl)?2H‐benzo[d][1,2,3]triazol‐4‐yl)‐[2,2′‐bithiophen]‐5‐yl)‐N‐(4‐(5‐methylthiophen‐2‐yl)phenyl)‐N‐phenylaniline ( P3 ) were synthesized to investigate the effect of TPA unit and π‐bridges on electrochemical and spectroelectrochemical properties of corresponding polymers. The synthesis was carried out via Stille coupling for P1 , P3 , and Suzuki coupling for P2 . Electrochemical and spectral results showed that P1 has an ambipolar character, in other words it is both p‐type and n‐type dopable, whereas P2 and P3 have only p‐doping property. Effect of different π‐bridges and TPA unit on the HOMO and LUMO energy levels, switching time, and optical contrast were discussed. All polymers are promising materials for electrochromic devices. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 537–544 |
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Keywords: | conjugated polymers donor– acceptor electrochemistry redox polymers triphenylamine π ‐bridge effect |
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