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Diborane heterolysis and P(v) reduction by Ph3P[double bond, length as m-dash]O coordination to magnesium
Anne-Frédérique Pécharman1, Nasir A Rajabi1, Michael S Hill1
1Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK. msh27@bath.ac.uk cm2025@bath.ac.uk.
Abstract:
Reaction of a magnesium diboranate complex with triphenylphosphine oxide provides a terminal magnesium boryl, which is itself a potent reagent for the deoxygenative reduction of Ph3PO. Computational analysis with density functional theory (DFT) indicates that B-B bond activation results from initial coordination of the P[double bond, length as m-dash]O bond of the phosphine oxide to magnesium.
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