Abstract
Reaction of group 12 metal chlorides with dialkylchalcogeno diamine [{NH2(CH2)nE(CH2)nNH2} (n=2 or 3 and E=Se and Te)] afforded the complexes [M2{NH2(CH2)nE(CH2)nNH2)}2Cl4] (M=Zn, Cd and Hg) and with CdI2 [Cd{NH2(CH2)nE(CH2)nNH2)}2] [Cdl4]. Complexes were characterized by elemental analyses, IR, 1H, 13C NMR, FAB mass and by single crystal X-ray structure determinations. In all the complexes, the ligand acts as a neutral tridentate (N, Se, N or N, Te, N) donor. Thermal analyses for the complexes were also performed by thermogravimetry.