Year

2017

Type(s)

Journal Article

Author(s)

Pander, P. and Motyka, R. and Zassowski, P. and Lapkowski, M. and Swist, A. and Data, P.

Source

Journal of Physical Chemistry C, 121(21): 11027—11036, 2017

Url

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85020475820&doi=10.1021%2facs.jpcc.7b00216&partnerID=40&md5=126953938a40c6f1078c23545f5cb5ba

BibTeX

BibTeX

BibTeX

@ARTICLE{Pander201711027, author={Pander, P. and Motyka, R. and Zassowski, P. and Lapkowski, M. and Swist, A. and Data, P.}, title={Electrochromic Properties of Novel Selenophene and Tellurophene Derivatives Based on Carbazole and Triphenylamine Core}, journal={Journal of Physical Chemistry C}, year={2017}, volume={121}, number={21}, pages={11027-11036}, doi={10.1021/acs.jpcc.7b00216}, note={cited By 2}, url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-85020475820&doi=10.1021%2facs.jpcc.7b00216&partnerID=40&md5=126953938a40c6f1078c23545f5cb5ba}, abstract={The 2,7- and 3,6-substituted carbazole and triphenylamine chalcogenophene (Se, Te) derivatives and their electrodeposited polymers are investigated using electrochemical and UV-vis-NIR/ESR spectroelectrochemical methods. Major differences in the case of oxidation and electropolymerization behavior between monomers and related polymers are shown. Se and Te atoms do not conjugate their lone electron pairs with the π-conjugated system and therefore only increase the contribution of the quinoid form of the chalcogenophene unit. The 2,7- substituted carbazole derivatives present stronger carbazole-chalcogenophene conjugation than 3,6-substituted derivatives. One 3,6-substituted carbazole derivative and triphenylamine derived polymers were found to have promising electrochromic properties with black electrochromism. © 2017 American Chemical Society.}, document_type={Article}, source={Scopus},