There are different reports on the coordination mode 1,3-thiazolidine-2-thione to metals with both N and S as donor atoms.
1Interest in the coordination chemistry of the 1,3-thiazole derivatives arises from the presence of the heterocyclic skeleton in many biomolecules. 2 The crystal structure on the metal complexes of this ligand is scarce.This ligand exhibits a thiol-thione tautomerism, as shown in the following thiol-thione equilibrium (N=C-SH and -NH-C=S) [Scheme 1].3 Deprotonation in a basic media produces the thionate moiety, which is capable of a monodentate, bidentate or bridging coordination behavior utilizing either sulfur or nitrogen atoms, or both of them, in the complexes. 4 Zinc and cadmium complexes with N2S2 ligand cores are of interest as structural and spectroscopic models for metal binding sites in a number of metallothioneins and metalloregulatory proteins. 1,3-Thiazolidine-2-thione and 2,2′-bipyridine were purchased from Across. All of the solvents were used without additional purification. A polymeric complex, [Cd(C3H4NS2)2], was prepared by the method described in the literature.
3The product, [Cd(C3H4NS2)2(bipy)], was synthesized by adding 2,2′-bipyridine (3.12 g, 0.02 mol) in chloroform-dimethylformamide (1:1, 20 mL) to a suspension of a polymeric complex, [Cd(C3H4NS2)2] (1.42 g, 0.005 mol), in chloroform (10 mL) at room temperature. After stirring for two hours, a yellow solution was formed and then filtered to remove traces of solids, and was finally allowed to stand at room temperature. After several days, colorless crystals were collected and washed with toluene under a nitrogen atmosphere. These crystals were sensitive to air and suitable for a crystallographic study. The