Reaction of the title ligands (HPyTSC and HS(S)PPh2, respectively) with R2S
nO (R = Me, Et, Bu) in ethanol (EtOH) afforded the complexes [SnMe2(PyTSC)
(S2PPh2) . EtOH (1) and [SnR2(PyTSC) (S2PPh2) ] (R = Et (2), Bu (3)). The s
tructures of 1 and 2 were determined by single-crystal X-ray diffractometry
. In both these complexes the tin atom is coordinated to an N,N,S-dentate t
hiosemicarbazonate ligand, an anisobidentate dithiophosphinato ligand and t
he two R groups. The coordination polyhedrons can be described as distorted
pentagonal bipyramids. A comparative study of the IR spectra of 1, 2 and 3
indicates that the butyl complex has a similar structure. Multinuclear (H-
1, C-13, P-31 and Sn-119) NMR data suggest that the structures of 1 and 2 p
robably remain in CDCl3 (or DMSO-d(6)) solution but compound 3 partially de
composes in these media. Preliminary results on the effects of the complexe
s on the proliferation and differentiation of FLC, GEM, U937, K562 and TOM-
1 leukaemia cells, and on the clonogenic activity of K562 cells are also de
scribed. (C) 1999 Elsevier Science Inc. All rights reserved.