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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...

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Autores principales: Mato, Mauro, Bruzzese, Paolo Cleto, Takahashi, Fumiya, Leutzsch, Markus, Reijerse, Edward J., Schnegg, Alexander, Cornella, Josep
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
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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.
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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
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