Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units

A benzo[ghi]perylenetriimide (BPTI) derivative bearing a terminal azido group on the expanded π-conjugated backbone has been synthesized and characterized. This promising photo- and electroactive BPTI motif has been used to obtain an original penta(organo)fullerene as a promising multi-electron acce...

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Autores principales: Drou, Clément, Merland, Théo, Busseau, Antoine, Dabos-Seignon, Sylvie, Goujon, Antoine, Hudhomme, Piétrick, Benyahia, Lazhar, Chassenieux, Christophe, Legoupy, Stéphanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694833/
https://www.ncbi.nlm.nih.gov/pubmed/35423142
http://dx.doi.org/10.1039/d1ra00287b
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author Drou, Clément
Merland, Théo
Busseau, Antoine
Dabos-Seignon, Sylvie
Goujon, Antoine
Hudhomme, Piétrick
Benyahia, Lazhar
Chassenieux, Christophe
Legoupy, Stéphanie
author_facet Drou, Clément
Merland, Théo
Busseau, Antoine
Dabos-Seignon, Sylvie
Goujon, Antoine
Hudhomme, Piétrick
Benyahia, Lazhar
Chassenieux, Christophe
Legoupy, Stéphanie
author_sort Drou, Clément
collection PubMed
description A benzo[ghi]perylenetriimide (BPTI) derivative bearing a terminal azido group on the expanded π-conjugated backbone has been synthesized and characterized. This promising photo- and electroactive BPTI motif has been used to obtain an original penta(organo)fullerene as a promising multi-electron acceptor system. Our studies show its self-assembly resulting from aggregation via π–π stacking interaction in solution and in the solid state.
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spelling pubmed-86948332022-04-13 Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units Drou, Clément Merland, Théo Busseau, Antoine Dabos-Seignon, Sylvie Goujon, Antoine Hudhomme, Piétrick Benyahia, Lazhar Chassenieux, Christophe Legoupy, Stéphanie RSC Adv Chemistry A benzo[ghi]perylenetriimide (BPTI) derivative bearing a terminal azido group on the expanded π-conjugated backbone has been synthesized and characterized. This promising photo- and electroactive BPTI motif has been used to obtain an original penta(organo)fullerene as a promising multi-electron acceptor system. Our studies show its self-assembly resulting from aggregation via π–π stacking interaction in solution and in the solid state. The Royal Society of Chemistry 2021-02-03 /pmc/articles/PMC8694833/ /pubmed/35423142 http://dx.doi.org/10.1039/d1ra00287b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Drou, Clément
Merland, Théo
Busseau, Antoine
Dabos-Seignon, Sylvie
Goujon, Antoine
Hudhomme, Piétrick
Benyahia, Lazhar
Chassenieux, Christophe
Legoupy, Stéphanie
Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units
title Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units
title_full Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units
title_fullStr Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units
title_full_unstemmed Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units
title_short Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units
title_sort synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694833/
https://www.ncbi.nlm.nih.gov/pubmed/35423142
http://dx.doi.org/10.1039/d1ra00287b
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