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Issue 14, 2011
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Reactivity of a platinum-substituted borirene

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Abstract

We report on (i) the reactivity of the title compound trans-[Cl(PMe3)2Pt{μ-BN(SiMe3)2C[double bond, length as m-dash]C}Ph] (1), which underwent a photochemical rearrangement reaction to afford the platinum boryl complex trans-[Cl(PMe3)2PtBN(SiMe3)2C[triple bond, length as m-dash]CPh] (2), (ii) a ring-opening reaction by chemoselective boron–carbon bond cleavage resulting in the amino(vinyl)borane trans-[Cl(PMe3)2PtCH[double bond, length as m-dash]C(BClN(SiMe3)2)Ph] (3), and (iii) a Cl–Br ligand exchange on the platinum atom yielding the Br-derivate trans-[Br(PMe3)2Pt{μ-BN(SiMe3)2C[double bond, length as m-dash]C}Ph] (4). All compounds were fully characterized by multinuclear NMR spectroscopy and single crystal X-ray diffraction analysis.

Graphical abstract: Reactivity of a platinum-substituted borirene

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Publication details

The article was received on 03 Dec 2010, accepted on 26 Jan 2011 and first published on 18 Feb 2011


Article type: Paper
DOI: 10.1039/C0DT01694B
Citation: Dalton Trans., 2011,40, 3666-3670
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    Reactivity of a platinum-substituted borirene

    H. Braunschweig, Q. Ye, K. Radacki and T. Kupfer, Dalton Trans., 2011, 40, 3666
    DOI: 10.1039/C0DT01694B

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