Abstract
The complexation reactions between TI +, Cd 2+, Hg 2+ and Pd 2+ ions and 18-crown-6 (18C6), 1,10-diaza-18-crown-6 (C22) and cryptand C222 were studied in various CH 3CN + H 2O mixtures at 22°C using dc and differential pulse polarographic techniques. The stoichiometry and stability of the complexes were determined by monitoring the shift in half-wave or peak potential of the polarographic waves of metal ions against the ligand concentration. In the cases where irreversible polarograms were observed for M 2+/M(Hg) systems, the reversible Hg 2+/Hg amalgam couple was used as an electrochemical probe for the study of M 2+ - ligand interactions. In all the solvent mixtures used, the stability of the resulting 1:1 complexes was found to vary in the order C222 > C22 > 18C6. The selectivity order for 18C6 complexes is Pb 2+ > Cd 2+ > Hg 2+ > Tl + while for the C22 and C222 complexes it is Hg 2+⪢ Pb 2+ > Cd 2+ > Tl +. There is an inverse relationship between the complex formation constants and the amount of water in the mixed solvent. In all cases, a linear relation was observed between log K f and the mole fraction of acetonitrile.
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