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

Citation
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
Citations number
69
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
35
Issue
26
Year of publication
1996
Pages
7691 - 7698
Database
ISI
SICI code
0020-1669(1996)35:26<7691:TS-XS>2.0.ZU;2-Y
Abstract
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.