Cargando…
meso-Antracenyl-BODIPY Dyad as a New Photocatalyst in Atom-Transfer Radical Addition Reactions
[Image: see text] We demonstrate that because of the efficient generation of triplet excited state under UV or visible-light irradiation, meso-antracenyl-BODIPY donor–acceptor dyad can catalyze atom-transfer radical addition (ATRA) reactions between bromomalonate and alkenes. This finding paves the...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655941/ https://www.ncbi.nlm.nih.gov/pubmed/34901630 http://dx.doi.org/10.1021/acsomega.1c04724 |
_version_ | 1784612179113148416 |
---|---|
author | Abuhadba, Sara Tsuji, Miu Mani, Tomoyasu Esipova, Tatiana V. |
author_facet | Abuhadba, Sara Tsuji, Miu Mani, Tomoyasu Esipova, Tatiana V. |
author_sort | Abuhadba, Sara |
collection | PubMed |
description | [Image: see text] We demonstrate that because of the efficient generation of triplet excited state under UV or visible-light irradiation, meso-antracenyl-BODIPY donor–acceptor dyad can catalyze atom-transfer radical addition (ATRA) reactions between bromomalonate and alkenes. This finding paves the way for the design and application of the new type of heavy atom-free organic chromophores for photocatalysis. |
format | Online Article Text |
id | pubmed-8655941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-86559412021-12-10 meso-Antracenyl-BODIPY Dyad as a New Photocatalyst in Atom-Transfer Radical Addition Reactions Abuhadba, Sara Tsuji, Miu Mani, Tomoyasu Esipova, Tatiana V. ACS Omega [Image: see text] We demonstrate that because of the efficient generation of triplet excited state under UV or visible-light irradiation, meso-antracenyl-BODIPY donor–acceptor dyad can catalyze atom-transfer radical addition (ATRA) reactions between bromomalonate and alkenes. This finding paves the way for the design and application of the new type of heavy atom-free organic chromophores for photocatalysis. American Chemical Society 2021-11-19 /pmc/articles/PMC8655941/ /pubmed/34901630 http://dx.doi.org/10.1021/acsomega.1c04724 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Abuhadba, Sara Tsuji, Miu Mani, Tomoyasu Esipova, Tatiana V. meso-Antracenyl-BODIPY Dyad as a New Photocatalyst in Atom-Transfer Radical Addition Reactions |
title | meso-Antracenyl-BODIPY Dyad as a
New Photocatalyst in Atom-Transfer Radical Addition Reactions |
title_full | meso-Antracenyl-BODIPY Dyad as a
New Photocatalyst in Atom-Transfer Radical Addition Reactions |
title_fullStr | meso-Antracenyl-BODIPY Dyad as a
New Photocatalyst in Atom-Transfer Radical Addition Reactions |
title_full_unstemmed | meso-Antracenyl-BODIPY Dyad as a
New Photocatalyst in Atom-Transfer Radical Addition Reactions |
title_short | meso-Antracenyl-BODIPY Dyad as a
New Photocatalyst in Atom-Transfer Radical Addition Reactions |
title_sort | meso-antracenyl-bodipy dyad as a
new photocatalyst in atom-transfer radical addition reactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655941/ https://www.ncbi.nlm.nih.gov/pubmed/34901630 http://dx.doi.org/10.1021/acsomega.1c04724 |
work_keys_str_mv | AT abuhadbasara mesoantracenylbodipydyadasanewphotocatalystinatomtransferradicaladditionreactions AT tsujimiu mesoantracenylbodipydyadasanewphotocatalystinatomtransferradicaladditionreactions AT manitomoyasu mesoantracenylbodipydyadasanewphotocatalystinatomtransferradicaladditionreactions AT esipovatatianav mesoantracenylbodipydyadasanewphotocatalystinatomtransferradicaladditionreactions |