Issue 8, 1981

Reactions and properties of some trimethyleneplatinum(IV) complexes. Part 11. Platinacyclobutanes derived from methylcyclopropane

Abstract

It is shown that platinacyclobutanes derived from methylcyclopropane exist as a mixture of isomers with partial structures [graphic omitted]H2 and [graphic omitted]HMe, and that these isomers interconvert easily. In some cases decomposition of these platinacyclobutanes gives ylide complexes [PtCl2{CH(L)CH2CH2Me}L], e.g. L = 2-methylpyridine, while in other cases but-1-ene complexes [PtCl2(CH2[double bond, length half m-dash]CHCH2Me)L], e.g. L = CD3CN, are formed. In both cases the products are formed selectively from the least stable isomer of the platinacyclobutane. At higher temperatures or on photolysis, platinacyclobutane complexes such as [PtCl2(C3H5Me)(1,10-phenanthroline)] decompose to give but-1-ene, 2-methylpropene, propene, and ethylene and the relative yields depend on the experimental conditions. Possible mechanisms are discussed.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1981, 1738-1745

Reactions and properties of some trimethyleneplatinum(IV) complexes. Part 11. Platinacyclobutanes derived from methylcyclopropane

R. J. Al-Essa, R. J. Puddephatt, D. C. L. Perkins, M. C. Rendle and C. F. H. Tipper, J. Chem. Soc., Dalton Trans., 1981, 1738 DOI: 10.1039/DT9810001738

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