Please use this identifier to cite or link to this item: 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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