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Contrasting reactivity of B–Cl and B–H bonds at [Ni(IMes) 2 ] to form unsupported Ni-boryls
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Contrasting reactivity of B–Cl and B–H bonds at [Ni(IMes) 2 ] to form unsupported Ni-boryls

Gabrielle Audsley, Ambre Carpentier, Anne-Frédérique Pécharman, James Wright, Thomas M Roseveare, Ewan R. Clark, Stuart A Macgregor and Ian Riddlestone
Chemical communications (Cambridge, England), Vol.60(7), pp.874-877
Winter 2024
PMID: 38164828

Abstract

Nickel; Boron; Transition Metal; Boryl; Density Functional theory
[Ni(IMes) 2 ] reacts with chloroboranes via oxidative addition to form rare unsupported Ni-boryls. In contrast, the oxidative addition of hydridoboranes is not observed and products from competing reaction pathways are identified. Computational studies relate these differences to the mechanism of oxidative addition: B–Cl activation proceeds via nucleophilic displacement of Cl − , while B–H activation would entail high energy concerted bond cleavage.
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