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Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization

Because of the importance of hydrogen atom transfer (HAT) in biology and chemistry, there is increased interest in new strategies to perform HAT in a sustainable manner. Here, we describe a sustainable, net redox-neutral HAT process involving hydrosilanes and alkali metal Lewis base catalysts — elim...

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Autores principales: Asgari, Parham, Hua, Yuanda, Bokka, Apparao, Thiamsiri, Chanachon, Prasitwatcharakorn, Watcharapon, Karedath, Ashif, Chen, Xin, Sardar, Sinjinee, Yum, Kyungsuk, Leem, Gyu, Pierce, Brad S., Nam, Kwangho, Gao, Jiali, Jeon, Junha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711469/
https://www.ncbi.nlm.nih.gov/pubmed/31460492
http://dx.doi.org/10.1038/s41929-018-0217-z
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author Asgari, Parham
Hua, Yuanda
Bokka, Apparao
Thiamsiri, Chanachon
Prasitwatcharakorn, Watcharapon
Karedath, Ashif
Chen, Xin
Sardar, Sinjinee
Yum, Kyungsuk
Leem, Gyu
Pierce, Brad S.
Nam, Kwangho
Gao, Jiali
Jeon, Junha
author_facet Asgari, Parham
Hua, Yuanda
Bokka, Apparao
Thiamsiri, Chanachon
Prasitwatcharakorn, Watcharapon
Karedath, Ashif
Chen, Xin
Sardar, Sinjinee
Yum, Kyungsuk
Leem, Gyu
Pierce, Brad S.
Nam, Kwangho
Gao, Jiali
Jeon, Junha
author_sort Asgari, Parham
collection PubMed
description Because of the importance of hydrogen atom transfer (HAT) in biology and chemistry, there is increased interest in new strategies to perform HAT in a sustainable manner. Here, we describe a sustainable, net redox-neutral HAT process involving hydrosilanes and alkali metal Lewis base catalysts — eliminating the use of transition metal catalysts — and report an associated mechanism concerning Lewis base-catalysed, complexation-induced HAT (LBCI-HAT). The catalytic LBCI-HAT is capable of accessing both branch-specific hydrosilylation and polymerization of vinylarenes in a highly selective fashion, depending on the Lewis base catalyst used. In this process, earth abundant, alkali metal Lewis base catalyst plays a dual role. It first serves as a HAT initiator and subsequently functions as a silyl radical stabilizing group, which is critical to highly selective cross-radical coupling. EPR study identified a potassiated paramagnetic species and multistate density function theory revealed a high HAT character, yet multiconfigurational nature in the transition state of the reaction.
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spelling pubmed-67114692019-08-27 Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization Asgari, Parham Hua, Yuanda Bokka, Apparao Thiamsiri, Chanachon Prasitwatcharakorn, Watcharapon Karedath, Ashif Chen, Xin Sardar, Sinjinee Yum, Kyungsuk Leem, Gyu Pierce, Brad S. Nam, Kwangho Gao, Jiali Jeon, Junha Nat Catal Article Because of the importance of hydrogen atom transfer (HAT) in biology and chemistry, there is increased interest in new strategies to perform HAT in a sustainable manner. Here, we describe a sustainable, net redox-neutral HAT process involving hydrosilanes and alkali metal Lewis base catalysts — eliminating the use of transition metal catalysts — and report an associated mechanism concerning Lewis base-catalysed, complexation-induced HAT (LBCI-HAT). The catalytic LBCI-HAT is capable of accessing both branch-specific hydrosilylation and polymerization of vinylarenes in a highly selective fashion, depending on the Lewis base catalyst used. In this process, earth abundant, alkali metal Lewis base catalyst plays a dual role. It first serves as a HAT initiator and subsequently functions as a silyl radical stabilizing group, which is critical to highly selective cross-radical coupling. EPR study identified a potassiated paramagnetic species and multistate density function theory revealed a high HAT character, yet multiconfigurational nature in the transition state of the reaction. 2019-01-28 2019-02 /pmc/articles/PMC6711469/ /pubmed/31460492 http://dx.doi.org/10.1038/s41929-018-0217-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Asgari, Parham
Hua, Yuanda
Bokka, Apparao
Thiamsiri, Chanachon
Prasitwatcharakorn, Watcharapon
Karedath, Ashif
Chen, Xin
Sardar, Sinjinee
Yum, Kyungsuk
Leem, Gyu
Pierce, Brad S.
Nam, Kwangho
Gao, Jiali
Jeon, Junha
Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization
title Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization
title_full Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization
title_fullStr Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization
title_full_unstemmed Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization
title_short Catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization
title_sort catalytic hydrogen atom transfer from hydrosilanes to vinylarenes for hydrosilylation and polymerization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711469/
https://www.ncbi.nlm.nih.gov/pubmed/31460492
http://dx.doi.org/10.1038/s41929-018-0217-z
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