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Addition of dihydrogen to a borylborenium center.

ABSTRACT: The activation of a H-H bond, the simplest covalent bond, is a fundamentally important process. Addition of H2 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 H2 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 H2 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.

SUBMITTER: Zheng J

PROVIDER: S-EPMC5883945 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

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Addition of dihydrogen to a borylborenium center.

Zheng Junhao J Li Zhen Hua ZH Wang Huadong H

Chemical science 20171128 6

The activation of a H-H bond, the simplest covalent bond, is a fundamentally important process. Addition of H<sub>2</sub> 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<sub>2</sub> 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 additio ...[more]

PMID: 29675190

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