Author:
Clare BW,Hefter G,Singh P
Abstract
Equilibrium constants for the formation of ZnCln2-n complexes have been measured in some acetonitrile ( MeCN )-water mixtures ranging from 0 to 100% MeCN at 25°C and I = 0.1 M (Et4NClO4), by potentiometric titration. The equilibria shift strongly in favour of the formation of the higher-order complexes (n = 3, 4) at high MeCN concentrations. This is shown to be due to differences in the magnitude of unfavourable solvation of the Zn2+, Cl - and ZnCln2-n ions in MeCN-H2O solutions. The Gibbs free energies of transfer of all of these ions from water to MeCN-H2O mixtures are strongly positive, but the net change in the transfer function for the formation of the higher-order complexes is favourable. Thus the formation of these complexes is predominant in MeCN -rich aqueous solutions. Approximate measurements in propiononitrile indicate that the ZnCln2-n complexes are even stronger than in acetonitrile.
Cited by
10 articles.
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