TRANS-CHLOROMETHYLBIS(DIMETHYL SULFOXIDE)PLATINUM(II) - X-RAY STRUCTURE, MECHANISM OF ISOMERIZATION, AND ITS USE AS A PRECURSOR TO ORGANOAMINE COMPLEXES OF VARIABLE GEOMETRICAL CONFIGURATIONS
R. Romeo et al., TRANS-CHLOROMETHYLBIS(DIMETHYL SULFOXIDE)PLATINUM(II) - X-RAY STRUCTURE, MECHANISM OF ISOMERIZATION, AND ITS USE AS A PRECURSOR TO ORGANOAMINE COMPLEXES OF VARIABLE GEOMETRICAL CONFIGURATIONS, Inorganic chemistry, 35(26), 1996, pp. 7691-7698
An unusual 2:1 aggregate between the complex trans-[PtCl(CH3)(DMSO)(2)
] (1; DMSO = dimethyl sulfoxide) and the organotin compound )bis(mu-di
methyltin(IV))bis(chlorodimethyltin(IV)) [Cl(CH3)(2)-SnOSn(CH3)(2)Cl](
2) has been isolated and characterized by X-ray analysis. The crystals
belong to the triclinic space group <P(1)over bar> with lattic consta
nts a = 9.373(2) Angstrom, b = 9.576(1) Angstrom, c = 14.087(3) Angstr
om, alpha = 70.29(1), beta = 75.50(1)degrees, gamma = 72.21(2)degrees,
and Z = 2. Least-squares refinement of the structure led to an R fact
or of 2.37%. H-1, C-13, and (195)PtNMR measurements revealed that in c
hloroform solution complex 1 gives a mixture of four different species
, which have been unambigously identified as the starting complex 1 in
equilbrium with cis-[PtCl(CH3)-(DMSO)(2)] and the two corresponding i
someric aqua-species cis and trans-[PtCl(CH3)(DMSO)(2)](OH2)]. The Pt-
195 NMR magnetization transfer technique allowed determination of the
rate of interconversion among the various complexes, showing that the
direct trans-cis isomerism between the [PtCl(CH3)DMSO)(2)] species is
negligible and that the geometrical interconversion occurs through a w
ater-catalyzed pathway. The exchange between free and coordinated DMSO
in cis- and trans-[PtCl(CH3)(DMSO)(2)] has been measured by H-1 NMR m
agnetization transfer experiments. The molecule of DMSO in the positio
n trans to a methyl group was found to be 10-fold more labile than tha
t trans to another sulfur bonded dimethyl sulfoxide. The reactivity of
complex 1 in chloroform with a series of monodentate nitrogen ligands
having widely different electronic and steric properties has been inv
estigated by H-1 NMR spectorscopy. The utility of this system as precu
rsor for the synthesis of cis and trans-[PtCl(CH3)(DMSO)(am)] is discu
ssed together with the evidence for the factors promoting the prevalen
ce of a geometrical configuration.