The synthesis and characterisation of [Pd(S2CNEt2) {Ph2P(CH2)(n) PPh2}](+)salts of some chlorometallate anions (n = 1, 3, 4): X-ray crystal structures of the salts [Pd(S2CNEt2){Ph2P(CH2)(n) PPh2}](2)[MCl4] (n = 1, 4; M = Cd; n = 3; M = Hg)
G. Exarchos et al., The synthesis and characterisation of [Pd(S2CNEt2) {Ph2P(CH2)(n) PPh2}](+)salts of some chlorometallate anions (n = 1, 3, 4): X-ray crystal structures of the salts [Pd(S2CNEt2){Ph2P(CH2)(n) PPh2}](2)[MCl4] (n = 1, 4; M = Cd; n = 3; M = Hg), POLYHEDRON, 19(12), 2000, pp. 1511-1517
The palladium complexes [PdCl2{Ph2P(CH2)(n)PPh2}] (n = 1, 3, 4) react with
the bi- and tri-valent metal diethyldithiocarbamates [M(S2CNEt2)(2)] (M = Z
n, Cd, Hg, Ph) and [Mn(S2CNEt2)(3)] in cold dichloromethane solution to aff
ord salts of the general form [Pd(S2CNEt2){Ph2P(CH2)(n)PPh2}](2)[MCl4] in a
lmost quantitative yield. X-ray crystal structures are reported for the sal
ts [Pd(S2CNEt2){Ph2P(CH2)(n)PPh2}](2)[MCl4] (n = 1, 4; M = Cd: n = 3, M = H
g). Structural parameters, IR and NMR spectroscopic data for these salts ar
e compared with similar data previously reported for salts of the related c
ation [Pd(S2CNEt2){Ph2P(CH2)(2)PPh2}](+). (C) 2000 Elsevier Science Ltd. Al
l rights reserved.