STEREOELECTRONIC PROPERTIES OF THE SULFINYL-SUBSTITUTED PHOSPHINE-LIGANDS - SYNTHESIS AND X-RAY STRUCTURE OF THE STABLE COMPLEX [PDCL2(PH(2)PCH(2)S(O)ME)(MEOH)]
Gh. Quek et al., STEREOELECTRONIC PROPERTIES OF THE SULFINYL-SUBSTITUTED PHOSPHINE-LIGANDS - SYNTHESIS AND X-RAY STRUCTURE OF THE STABLE COMPLEX [PDCL2(PH(2)PCH(2)S(O)ME)(MEOH)], Inorganica Chimica Acta, 239(1-2), 1995, pp. 185-188
The square-planar complex trans-[PdCl2{Ph(2)PCH(2)S(O)Me}{MeOH}] has b
een prepared. The compound crystallizes as orange-red prisms in the mo
noclinic space group P2(1)/n, with a = 9.446(2), b = 14.858(3), c = 13
.578(3) Angstrom, beta = 105.08(2)degrees and Z = 4. The structure was
determined by direct methods and refined to R = 0.027 and R(w) = 0.04
1. All atoms including hydrogens were located directly from Fourier di
fference maps. The coordination geometry around palladium is square-pl
anar. The metal is coordinated to the two chlorines, the oxygen of met
hanol and the phosphorus of the sulfinyl-substituted ligand. In soluti
on, a similar structure is assigned to the complex by NMR studies. In
contrast to the previously documented Ph(2)PCH(2)CH(2)S(O)Me analogue,
the sulfoxide function in the Ph(2)PCH(2)S(O)Me ligand is not involve
d in any coordination bondings with palladium, both in the solid state
and in solution.