Open-[60]fullerene–aniline conjugates with near-infrared absorption

Two open-[60]fullerene–aniline conjugates were synthesized, in which the two-fold addition of diamine gave a thiazolidine-2-thione ring on the [60]fullerene cage in the presence of CS(2). By increasing the number of N,N-dimethylaniline moieties, the absorption edge was considerably shifted up to 120...

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Detalles Bibliográficos
Autores principales: Sadai, Shumpei, Hashikawa, Yoshifumi, Murata, Yasujiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177950/
https://www.ncbi.nlm.nih.gov/pubmed/37188248
http://dx.doi.org/10.1039/d3ra02113k
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author Sadai, Shumpei
Hashikawa, Yoshifumi
Murata, Yasujiro
author_facet Sadai, Shumpei
Hashikawa, Yoshifumi
Murata, Yasujiro
author_sort Sadai, Shumpei
collection PubMed
description Two open-[60]fullerene–aniline conjugates were synthesized, in which the two-fold addition of diamine gave a thiazolidine-2-thione ring on the [60]fullerene cage in the presence of CS(2). By increasing the number of N,N-dimethylaniline moieties, the absorption edge was considerably shifted up to 1200 nm owing to effective acceptor–donor interactions.
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spelling pubmed-101779502023-05-13 Open-[60]fullerene–aniline conjugates with near-infrared absorption Sadai, Shumpei Hashikawa, Yoshifumi Murata, Yasujiro RSC Adv Chemistry Two open-[60]fullerene–aniline conjugates were synthesized, in which the two-fold addition of diamine gave a thiazolidine-2-thione ring on the [60]fullerene cage in the presence of CS(2). By increasing the number of N,N-dimethylaniline moieties, the absorption edge was considerably shifted up to 1200 nm owing to effective acceptor–donor interactions. The Royal Society of Chemistry 2023-05-12 /pmc/articles/PMC10177950/ /pubmed/37188248 http://dx.doi.org/10.1039/d3ra02113k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Sadai, Shumpei
Hashikawa, Yoshifumi
Murata, Yasujiro
Open-[60]fullerene–aniline conjugates with near-infrared absorption
title Open-[60]fullerene–aniline conjugates with near-infrared absorption
title_full Open-[60]fullerene–aniline conjugates with near-infrared absorption
title_fullStr Open-[60]fullerene–aniline conjugates with near-infrared absorption
title_full_unstemmed Open-[60]fullerene–aniline conjugates with near-infrared absorption
title_short Open-[60]fullerene–aniline conjugates with near-infrared absorption
title_sort open-[60]fullerene–aniline conjugates with near-infrared absorption
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177950/
https://www.ncbi.nlm.nih.gov/pubmed/37188248
http://dx.doi.org/10.1039/d3ra02113k
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AT hashikawayoshifumi open60fullereneanilineconjugateswithnearinfraredabsorption
AT muratayasujiro open60fullereneanilineconjugateswithnearinfraredabsorption

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