A monoanionic, bidentate phosphaalkenyl–phosphido ligand was designed, synthesized, and used for the complexation of a rhodium carbonyl fragment. The characterization of the latter revealed delocalized π electrons on the phosphaalkenyl–phosphide moiety. The catalytic activity of this rhodium carbonyl complex has been demonstrated in a hydrosilylation reaction.
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Matsumoto et al. (2014) studied this question.
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