Abstract
A series of dithienothiophene-based electrochromic polymers are synthesized by a Stille coupling reaction of 2,6-bis(trimethylstannyl)dithieno[3,2-b:2′,3′-d]thiophene, 2,5-dibromo-3,4-bis(dodecyloxy)thiophene, and tris(4-bromophenylamine). The resulting polymers have high molecular weights in the range of 59200 to 81300?gmol-1, and good solubility in common organic solvents. The polymer films are purple/red in neutral states and gradually become gray when oxidized to an intermediate state and blue when fully oxidized. Incorporation of triphenylamine into the polymer chains has resulted in a significant increase in the redox stability, which renders this a potential method to create high-performance electrochromic polymers.
Original language | English |
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Pages (from-to) | 1306-1311 |
Number of pages | 6 |
Journal | ChemPlusChem |
Volume | 80 |
Issue number | 8 |
DOIs | |
Publication status | Published - Aug 1 2015 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
ASJC Scopus Subject Areas
- General Chemistry
Keywords
- electrochromism
- heterocycles
- polymers
- structure-activity relationship
- synthesis design