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Effect of random copolymerization on the optical properties of selenophene and thieno[3,4-c]pyrrole-4,6-dione conjugated polymers
Date
2022-07-01
Author
Yasa, Mustafa
UDUM, YASEMİN
Toppare, Levent Kamil
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© 2022For the preparation of conjugated polymers having targeted band gaps, absorption, and optoelectronic properties, the Donor-Acceptor (D-A) approach has been one of the most convenient methods. We synthesized four new conjugated polymers, bearing selenophene and thieno[3,4-c]pyrrole-4,6-dione (TPD) for this study via Suzuki Stille Polycondensation. The effect of selenophene that was inserted as π-bridge and the introduction of a second TPD unit into the polymer backbones through random polymerization were investigated. Optoelectronic properties of the polymers were analyzed via electrochemical and spectroelectrochemical studies. The study reveals the effects of TPD and selenophene moieties on absorption and band gaps of the polymer and provides a concise approach for the preparation of D-A conjugated polymers.
Subject Keywords
Band gap
,
Conjugated polymers
,
Electrochromism
,
Suzuki Polycondensation
,
Thieno[3,4-c]pyrrole-4,6-dione
URI
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85127013311&origin=inward
https://hdl.handle.net/11511/97605
Journal
Microchemical Journal
DOI
https://doi.org/10.1016/j.microc.2022.107395
Collections
Department of Chemistry, Article
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M. Yasa, Y. UDUM, and L. K. Toppare, “Effect of random copolymerization on the optical properties of selenophene and thieno[3,4-c]pyrrole-4,6-dione conjugated polymers,”
Microchemical Journal
, vol. 178, pp. 0–0, 2022, Accessed: 00, 2022. [Online]. Available: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85127013311&origin=inward.