A B-C double bond unit coordinated to platinum: an alkylideneboryl ligand that is isoelectronic to neutral aminoborylene Ligands.

Angew Chem Int Ed Engl

Institut für Anorganische Chemie, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg (Germany) http://www-anorganik.chemie.uni-wuerzburg.de/Braunschweig/

Published: February 2014

The reaction of [Pt(PCy3)2] with Br2B-CH(SiMe3)2 resulted in generation of the first alkylideneboryl complex, trans-[Br(Cy3P)2Pt{B=CH(SiMe3)}], with concomitant elimination of Me3 SiBr. The trans bromide ligand of the alkylideneboryl complex was readily substituted by a methyl group upon treatment with methyllithium, leading to another alkylideneboryl complex, trans-[Me(Cy3P)2Pt{B=CH(SiMe3)}]. Various spectrochemical techniques, single-crystal X-ray crystallography, and quantum chemical calculations confirmed the formulation of a double bond between the boron and the carbon atom. The theoretical studies also provided evidence for the stronger trans influence of the alkylideneboryl ligand over iminoboryl and oxoboryl ligands.

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http://dx.doi.org/10.1002/anie.201310557DOI Listing

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