Investigating the impact of substitution on the optoelectronic properties of benzothiophenone <i>S,S</i> -dioxide

Dyes were synthesized from 3,5,6-tribromobenzothiophene S,S -dioxide via a versatile intermediate enabling couplings, condensations, and conjugation, yielding IR-absorbing dyes tunable as donors or acceptors with LUMO ≈ −4 eV for solar cells.

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Journal
New Journal of Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5nj02518d
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Investigating the impact of substitution on the optoelectronic properties of benzothiophenone S,S -dioxide

Frédéric Gohier, E. Levillain, Hayley Melville, Charles Cougnon et al.
New Journal of Chemistry
Organic Chemistry Cycloaddition Reactions
article

Investigating the impact of substitution on the optoelectronic properties of benzothiophenone S,S -dioxide

Frédéric Gohier, E. Levillain, Hayley Melville, Charles Cougnon, Lionel Sanguinet, Magali Allain, Khaled Youssef
article en

Abstract

Dyes were synthesized from 3,5,6-tribromobenzothiophene S,S -dioxide via a versatile intermediate enabling couplings, condensations, and conjugation, yielding IR-absorbing dyes tunable as donors or acceptors with LUMO ≈ −4 eV for solar cells.

New Journal of ChemistryVol. 49(35)
Centre National de la Recherche Scientifique (FR), Institut des Sciences et Technologies Moléculaires d'Angers (FR)
Angers Loire Métropole
Openalex Percentile: Top 85%
Organic Chemistry Cycloaddition Reactions
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