Cargando…
Oxidative Addition of Aryl Electrophiles into a Red-Light-Active Bismuthinidene
[Image: see text] The oxidative addition of aryl electrophiles is a fundamental organometallic reaction widely applied in the field of transition metal chemistry and catalysis. However, the analogous version based on main group elements still remains largely underexplored. Here, we report the abilit...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472430/ https://www.ncbi.nlm.nih.gov/pubmed/37603853 http://dx.doi.org/10.1021/jacs.3c06651 |
_version_ | 1785100074679795712 |
---|---|
author | Mato, Mauro Bruzzese, Paolo Cleto Takahashi, Fumiya Leutzsch, Markus Reijerse, Edward J. Schnegg, Alexander Cornella, Josep |
author_facet | Mato, Mauro Bruzzese, Paolo Cleto Takahashi, Fumiya Leutzsch, Markus Reijerse, Edward J. Schnegg, Alexander Cornella, Josep |
author_sort | Mato, Mauro |
collection | PubMed |
description | [Image: see text] The oxidative addition of aryl electrophiles is a fundamental organometallic reaction widely applied in the field of transition metal chemistry and catalysis. However, the analogous version based on main group elements still remains largely underexplored. Here, we report the ability of a well-defined organobismuth(I) complex to undergo formal oxidative addition with a wide range of aryl electrophiles. The process is facilitated by the reactivity of both the ground and excited states of N,C,N-bismuthinidenes upon absorption of low-energy red light. |
format | Online Article Text |
id | pubmed-10472430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104724302023-09-02 Oxidative Addition of Aryl Electrophiles into a Red-Light-Active Bismuthinidene Mato, Mauro Bruzzese, Paolo Cleto Takahashi, Fumiya Leutzsch, Markus Reijerse, Edward J. Schnegg, Alexander Cornella, Josep J Am Chem Soc [Image: see text] The oxidative addition of aryl electrophiles is a fundamental organometallic reaction widely applied in the field of transition metal chemistry and catalysis. However, the analogous version based on main group elements still remains largely underexplored. Here, we report the ability of a well-defined organobismuth(I) complex to undergo formal oxidative addition with a wide range of aryl electrophiles. The process is facilitated by the reactivity of both the ground and excited states of N,C,N-bismuthinidenes upon absorption of low-energy red light. American Chemical Society 2023-08-21 /pmc/articles/PMC10472430/ /pubmed/37603853 http://dx.doi.org/10.1021/jacs.3c06651 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Mato, Mauro Bruzzese, Paolo Cleto Takahashi, Fumiya Leutzsch, Markus Reijerse, Edward J. Schnegg, Alexander Cornella, Josep Oxidative Addition of Aryl Electrophiles into a Red-Light-Active Bismuthinidene |
title | Oxidative
Addition of Aryl Electrophiles into a Red-Light-Active
Bismuthinidene |
title_full | Oxidative
Addition of Aryl Electrophiles into a Red-Light-Active
Bismuthinidene |
title_fullStr | Oxidative
Addition of Aryl Electrophiles into a Red-Light-Active
Bismuthinidene |
title_full_unstemmed | Oxidative
Addition of Aryl Electrophiles into a Red-Light-Active
Bismuthinidene |
title_short | Oxidative
Addition of Aryl Electrophiles into a Red-Light-Active
Bismuthinidene |
title_sort | oxidative
addition of aryl electrophiles into a red-light-active
bismuthinidene |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472430/ https://www.ncbi.nlm.nih.gov/pubmed/37603853 http://dx.doi.org/10.1021/jacs.3c06651 |
work_keys_str_mv | AT matomauro oxidativeadditionofarylelectrophilesintoaredlightactivebismuthinidene AT bruzzesepaolocleto oxidativeadditionofarylelectrophilesintoaredlightactivebismuthinidene AT takahashifumiya oxidativeadditionofarylelectrophilesintoaredlightactivebismuthinidene AT leutzschmarkus oxidativeadditionofarylelectrophilesintoaredlightactivebismuthinidene AT reijerseedwardj oxidativeadditionofarylelectrophilesintoaredlightactivebismuthinidene AT schneggalexander oxidativeadditionofarylelectrophilesintoaredlightactivebismuthinidene AT cornellajosep oxidativeadditionofarylelectrophilesintoaredlightactivebismuthinidene |