Abstract

The complexes [Pt(ER)2(L–L)[ER = SPri, SPh, C6H4Me-p or SePh; L–L = Ph2P(Ch2)nPPh2(n= 1–3)] have been prepared and their ability to act as bidentate ligands towards other metal species demonstrated. Proton, 31P and 195Pt NMR spectroscopy have been employed to ascertain their structures. A single-crystal X-ray structure determination of [Pt(SePh)2(Ph2PCH2PPh2)] has established the mononuclear nature of the complex. The platinum atom is in a distorted square-planar environment with the selenium atoms and the chelating diphosphine ligand in a cis configuration. The four-membered PtPCP metallacyclic ring is non-planar.

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