Complexes of heterocyclic thiones and Group 12 metals Part 5. Reactions of1,3-thiazolidine-2-thione and benzo-1,3-thiazoline-2-thione with mercury(II) halides in a 2 : 1 ratio. Crystal structures of bis(1,3-thiazolidine-2-thione) mercury(II) bromide and bis(benzo-1,3-thiazolinato)mercury(II)
Na. Bell et al., Complexes of heterocyclic thiones and Group 12 metals Part 5. Reactions of1,3-thiazolidine-2-thione and benzo-1,3-thiazoline-2-thione with mercury(II) halides in a 2 : 1 ratio. Crystal structures of bis(1,3-thiazolidine-2-thione) mercury(II) bromide and bis(benzo-1,3-thiazolinato)mercury(II), INORG CHIM, 323(1-2), 2001, pp. 69-77
Reactions of mercury(II) halides with 1,3-thiazolidine-2-thione (tzdSH) and
benzo-1,3-thiazoline-2-thione (bztzSH) in aqueous ethanol produced the 1:2
complexes with the former ligand but, due to steric effects, only the prev
iously described 1: 1 complexes of the latter were isolated. Vibrational an
d C-13 NMR spectral studies indicate eta (1)-thione donation by the heteroc
yclic ligand and this has been confirmed by the crystal structure determina
tion of (tzdSH)(2)HgBr2. The structure consists of pseudotetrahedral mercur
y (II) with longer C-S and shorter C-N bonds than in the free ligand and wi
th the Br-Hg-Br angle being similar to 20 degrees smaller than the largest
angle, S-Hg-S, around mercury due to deformation by inter- and intra-molecu
lar interactions. The heterocyclic ligands are unsymmetrical round mercury
relative to the two bromines. Reaction of the two thiones with mercury(II)
acetate in ethanol in the presence of triethylamine results in deprotonatio
n with the formation of the corresponding thionates. The former produced in
soluble (tzdS)(2)Hg while the latter formed plate-like (bztzS)(2)Hg whose c
rystal structure showed linearity around mercury with digonal coordination
via the thionate sulphur. The small Hg-S-C angle and (HgN)-N-... separation
are indicative of a weak interaction between mercury and the nitrogen of t
he thioamide double bond. (C) 2001 Elsevier Science B.V. All rights reserve
d.