Abstract
Platinum(II) acetylides of the type trans-[Pt(CCR) 2(PMe 2Ph) 2] (R = CH 2OMe, CMe 2OH, Ph) are reduced by hydrazine hydrate to dialkenylplatinum(II) complexes of the type trans-[Pt(CHCHR) 2(PMe 2Ph) 2] in which the hydrogens are mutually cis on the alkenyl double bonds. Some of the complexes exist as rotational isomers in solution due to restricted rotation about the PtC single bonds. Mono-alkenyl complexes [PtCl(CHCHR)(PMe 2Ph) 2] (R = Ph or CMe 2OH) were prepared by the hydrogen chloride fission of the dialkenyl complexes. trans-[PtCl(CClCHCH 2OMe)(PMe 2Ph) 2] is formed when trans- [Pt(CCCH 2OMe) 2(PMe 2Ph) 2] is treated with hydrogen chloride whereas similar treatment of [Pt(CCCMe 2OH)(PMe 2Ph) 2] gives [PtCl(CClCHCMeCH 2)(PMe 2Ph) 2]. 1H, 13C and 31P NMR data are given and discussed.
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