Issue 13, 2001

A combinatorial-like probe on the reactivity of the {Pt2S2} core of Pt2(PPh3)4(μ-S)2 by electrospray mass spectrometry. Synthesis and structures of novel heterometallic sulfide aggregates of gold(III), mercury(II), and tin(IV) with platinum(II)

Abstract

Electrospray mass spectrometry (ESMS) provides a rapid and convenient technique for probing the nucleophilicity of the {Pt2S2} “butterfly” core. Positive-ion electrospray mass spectra have been recorded for a wide array of aggregates incorporating various metallo-fragments into the Pt2(PPh3)4(μ-S)21 moiety. Such combinatorial-like screening allowed a large number of different metal–sulfur interactions to be studied and the resultant heterometallic aggregates postulated. Such postulations were subsequently confirmed by synthetic studies and single-crystal X-ray crystallographic analyses. This approach helped to minimize the “wastage” by focusing on the synthesis of aggregates that were supported by the ESMS evidence. It has resulted in the isolation of a series of novel aggregates such as {AuIIIPt2S2}, {HgIIPt2S2}, and {SnIVPt2S2} in good lab-scale yields. It also led to the trapping and characterization of the monoprotonated product of 1, which has eluded isolation.

Graphical abstract: A combinatorial-like probe on the reactivity of the {Pt2S2} core of Pt2(PPh3)4(μ-S)2 by electrospray mass spectrometry. Synthesis and structures of novel heterometallic sulfide aggregates of gold(III), mercury(II), and tin(IV) with platinum(II)

Supplementary files

Article information

Article type
Paper
Submitted
23 Jan 2001
Accepted
09 May 2001
First published
18 Jun 2001

J. Chem. Soc., Dalton Trans., 2001, 1986-2002

A combinatorial-like probe on the reactivity of the {Pt2S2} core of Pt2(PPh3)4(μ-S)2 by electrospray mass spectrometry. Synthesis and structures of novel heterometallic sulfide aggregates of gold(III), mercury(II), and tin(IV) with platinum(II)

S.-W. Audi Fong, W. Teck Yap, J. J. Vittal, T. S. A. Hor, W. Henderson, A. G. Oliver and C. E. F. Rickard, J. Chem. Soc., Dalton Trans., 2001, 1986 DOI: 10.1039/B100789K

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