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https://hdl.handle.net/10356/168879
Title: | Non-fullerene electron acceptors based on hybridisation of corannulene and thiophene-S,S-dioxide motifs | Authors: | Báti, Gábor Csókás, Dániel Giurgi, Gavril-Ionel Zhou, Jingsong Szolga, Lorant A. Webster, Richard David Stuparu, Mihaiela Corina |
Keywords: | Science::Chemistry | Issue Date: | 2023 | Source: | Báti, G., Csókás, D., Giurgi, G., Zhou, J., Szolga, L. A., Webster, R. D. & Stuparu, M. C. (2023). Non-fullerene electron acceptors based on hybridisation of corannulene and thiophene-S,S-dioxide motifs. Chemistry (Weinheim An Der Bergstrasse, Germany), 29(18), e202203856-. https://dx.doi.org/10.1002/chem.202203856 | Project: | MOET1 RG11/21 MOE-T2EP10221-0002 |
Journal: | Chemistry (Weinheim an der Bergstrasse, Germany) | Abstract: | Herein we show that hybridisation of buckybowl corannulene and thiophene-S,S-dioxide motifs is a general approach for the preparation of high electron affinity molecular materials. The devised synthesis is modular and relies on thienannulation of corannnulene-based phenylacetylene scaffolds. The final compounds are highly soluble in common organic solvents. These compounds also exhibit interesting optical properties such as absorption and emission in the blue/green regions of the electromagnetic spectrum. Importantly, a bis-S,S-dioxide derivative exhibits three reversible reductions similar in their strength to the prevalent fullerene-based electron acceptor phenyl-C61 -butyric acid methyl ester (PC61 BM). | URI: | https://hdl.handle.net/10356/168879 | ISSN: | 0947-6539 | DOI: | 10.1002/chem.202203856 | Schools: | School of Chemistry, Chemical Engineering and Biotechnology | Rights: | © 2023 Wiley-VCH GmbH. All rights reserved. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | CCEB Journal Articles |
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