A Di-Substituted Boron Dication and Its Hydride-Induced Transformation to an NHC-Stabilized Borabenzene

A Di-Substituted Boron Dication and Its Hydride-Induced Transformation to an NHC-Stabilized Borabenzene

Give me a B: A stepwise chloride ion of [Cp*BCl2(IMes)] resulted in the linear di‐substituted boron dication [Cp*B(IMes)]2+. The hypercoordinated boron dication, stabilized in the pentagonal pyramidal [C5B]2+ cluster, reacts with superhydride to yield the N‐heterocyclic carbene‐stabilized borabenzen...

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Veröffentlicht in:Angewandte Chemie International Edition 2013-12, Vol.52 (50), p.13293-13297
Hauptverfasser: Shen, Chao-Tang, Liu, Yi-Hung, Peng, Shie-Ming, Chiu, Ching-Wen
Format: Artikel
Sprache:eng
Schlagworte:
Boron
cations
Chlorides
Clusters
heterocycles
N-heterocyclic carbenes
Transformations
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container_issue 50
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container_title Angewandte Chemie International Edition
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creator Shen, Chao-Tang
Liu, Yi-Hung
Peng, Shie-Ming
Chiu, Ching-Wen
description Give me a B: A stepwise chloride ion of [Cp*BCl2(IMes)] resulted in the linear di‐substituted boron dication [Cp*B(IMes)]2+. The hypercoordinated boron dication, stabilized in the pentagonal pyramidal [C5B]2+ cluster, reacts with superhydride to yield the N‐heterocyclic carbene‐stabilized borabenzene, [C5Me5B(IMes)] (see scheme).
doi_str_mv 10.1002/anie.201308385
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subjects Boron
cations
Chlorides
Clusters
heterocycles
N-heterocyclic carbenes
Transformations
title A Di-Substituted Boron Dication and Its Hydride-Induced Transformation to an NHC-Stabilized Borabenzene
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