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Addition of dihydrogen to a borylborenium center

The activation of a H–H bond, the simplest covalent bond, is a fundamentally important process. Addition of H(2) to an elemental center typically occurs on low valent transition metal or main group complexes through oxidative addition to afford metal dihydride complexes. In contrast, activation of H...

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Detalles Bibliográficos
Autores principales: Zheng, Junhao, Li, Zhen Hua, Wang, Huadong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883945/
https://www.ncbi.nlm.nih.gov/pubmed/29675190
http://dx.doi.org/10.1039/c7sc04987k
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author Zheng, Junhao
Li, Zhen Hua
Wang, Huadong
author_facet Zheng, Junhao
Li, Zhen Hua
Wang, Huadong
author_sort Zheng, Junhao
collection PubMed
description The activation of a H–H bond, the simplest covalent bond, is a fundamentally important process. Addition of H(2) to an elemental center typically occurs on low valent transition metal or main group complexes through oxidative addition to afford metal dihydride complexes. In contrast, activation of H(2) on a high valent center generally results in heterolytic cleavage of the H–H bond to a proton and hydride. Here, we report experimental and computational evidence for the addition of H(2) to a borenium center in an N-heterocyclic carbene (NHC) coordinated borylborenium cation, which leads to the formation of a dihydroborenium complex accompanied by the elimination of two σ-bonded substituents, namely mesityl (Mes) and pinacolboryl (Bpin) groups, as mesitylboronic ester.
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spelling pubmed-58839452018-04-19 Addition of dihydrogen to a borylborenium center Zheng, Junhao Li, Zhen Hua Wang, Huadong Chem Sci Chemistry The activation of a H–H bond, the simplest covalent bond, is a fundamentally important process. Addition of H(2) to an elemental center typically occurs on low valent transition metal or main group complexes through oxidative addition to afford metal dihydride complexes. In contrast, activation of H(2) on a high valent center generally results in heterolytic cleavage of the H–H bond to a proton and hydride. Here, we report experimental and computational evidence for the addition of H(2) to a borenium center in an N-heterocyclic carbene (NHC) coordinated borylborenium cation, which leads to the formation of a dihydroborenium complex accompanied by the elimination of two σ-bonded substituents, namely mesityl (Mes) and pinacolboryl (Bpin) groups, as mesitylboronic ester. Royal Society of Chemistry 2017-11-28 /pmc/articles/PMC5883945/ /pubmed/29675190 http://dx.doi.org/10.1039/c7sc04987k Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Zheng, Junhao
Li, Zhen Hua
Wang, Huadong
Addition of dihydrogen to a borylborenium center
title Addition of dihydrogen to a borylborenium center
title_full Addition of dihydrogen to a borylborenium center
title_fullStr Addition of dihydrogen to a borylborenium center
title_full_unstemmed Addition of dihydrogen to a borylborenium center
title_short Addition of dihydrogen to a borylborenium center
title_sort addition of dihydrogen to a borylborenium center
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883945/
https://www.ncbi.nlm.nih.gov/pubmed/29675190
http://dx.doi.org/10.1039/c7sc04987k
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