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Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air

The photoreactivity of anthracene has been previously verified for a range of its derivatives. 9,10-Dibutoxyanthracene is commonly used as an electron transfer sensitizer for photopolymerization because of its favorable optical properties. This study experimentally demonstrated that 9,10-dibutoxyant...

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Autores principales: Seto, Ryotaro, Sato, Arisa, Iuchi, Keita, Himori, Shunichi, Gotoh, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916649/
https://www.ncbi.nlm.nih.gov/pubmed/35275906
http://dx.doi.org/10.1371/journal.pone.0263526
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author Seto, Ryotaro
Sato, Arisa
Iuchi, Keita
Himori, Shunichi
Gotoh, Hiroaki
author_facet Seto, Ryotaro
Sato, Arisa
Iuchi, Keita
Himori, Shunichi
Gotoh, Hiroaki
author_sort Seto, Ryotaro
collection PubMed
description The photoreactivity of anthracene has been previously verified for a range of its derivatives. 9,10-Dibutoxyanthracene is commonly used as an electron transfer sensitizer for photopolymerization because of its favorable optical properties. This study experimentally demonstrated that 9,10-dibutoxyanthracene produces an endoperoxide species upon reaction with the oxygen present in air. A secondary decomposition product formed during the photodecomposition of the endoperoxide species was also isolated and identified. The proposed reaction pathway is supported by singlet oxygen scavenger studies and calculations of the singlet–triplet transition energies. Our findings suggest that 9,10-dibutoxyanthracene can be used as a photo-induced oxygen scavenger.
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spelling pubmed-89166492022-03-12 Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air Seto, Ryotaro Sato, Arisa Iuchi, Keita Himori, Shunichi Gotoh, Hiroaki PLoS One Research Article The photoreactivity of anthracene has been previously verified for a range of its derivatives. 9,10-Dibutoxyanthracene is commonly used as an electron transfer sensitizer for photopolymerization because of its favorable optical properties. This study experimentally demonstrated that 9,10-dibutoxyanthracene produces an endoperoxide species upon reaction with the oxygen present in air. A secondary decomposition product formed during the photodecomposition of the endoperoxide species was also isolated and identified. The proposed reaction pathway is supported by singlet oxygen scavenger studies and calculations of the singlet–triplet transition energies. Our findings suggest that 9,10-dibutoxyanthracene can be used as a photo-induced oxygen scavenger. Public Library of Science 2022-03-11 /pmc/articles/PMC8916649/ /pubmed/35275906 http://dx.doi.org/10.1371/journal.pone.0263526 Text en © 2022 Seto et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Seto, Ryotaro
Sato, Arisa
Iuchi, Keita
Himori, Shunichi
Gotoh, Hiroaki
Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air
title Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air
title_full Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air
title_fullStr Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air
title_full_unstemmed Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air
title_short Mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air
title_sort mechanism for the photodegradation of 9,10-dibutoxyanthracene in the presence of air
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916649/
https://www.ncbi.nlm.nih.gov/pubmed/35275906
http://dx.doi.org/10.1371/journal.pone.0263526
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