The complexation of Cd2+ by diallyl disulfide (DADS) and diallyl sulfide (DAS) has been studied by differential pulse voltammetry. Stability constants, (log b), of the 1: 1 (PbL) and 1: 2 (PbL2) complexes, where L=ligand, were found to be in the range of ca.5.8 - 6.2 and 9.6 -10.6, respectively. Complex formation is accompanied with a significant decrease in the peak current and the shift of the Cd2+/Cd half-wave potential to a higher one upon the addition of the sulfur containing ligands (L). The formation of 1: 1 and 1: 2 complexes, i.e., CdL2+ and CdL22+ was observed in the case of the two ligands. The consecutive formation constants of labile lead complexes with DADS and DAS were determined at 298K by the method of DeFord and Hume. Apparently due to the large size of the cadmium ion, steric hindrance caused by the greater steric bulk of DADS compared to that of DAS have little or no effects on the formation constants, so that very similar values were obtained in the case of the two ligands. Also, the possible participation of C=C double bonds in coordination with the metal center in the case of DADS appears to compensate for the steric effects caused by the larger size of this ligand. In agreement with the Jorgensen principle of symbiosis, the second formation constants were found to be approximately six orders of magnitude greater than the first ones.