Abstract
Stability constants of nickel(II) glycylglycinate complexes in aqueous solutions of dimethylsulfoxide of variable composition (from 0.00 to 0.60 mole fractions DMSO) are determined according to potentiometry at 298.15 K and an ionic strength of 0.1 M (NaClO4). It is determined that with a rise in the concentration of an organic cosolvent in solution, the stability of nickel(II) complexes with glycylglycinate ion on the whole increases, but the logK stability = f(X DMSO) dependences are of a critical character with a maximum of 0.3 mole fractions DMSO. It is demonstrated that the rise in the stability of complexes is related to the destabilization of ligands in the low concentration range of the organic component, while the presence of a maximum is due to the different dynamics of the solvation contributions from reagents during changes in the Gibbs energy of reaction.
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Original Russian Text © V.V. Naumov, V.A. Isaeva, Yu.A. Kovaleva, V.A. Sharnin, 2013, published in Zhurnal Fizicheskoi Khimii, 2013, Vol. 87, No. 7, pp. 1160–1163.
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Naumov, V.V., Isaeva, V.A., Kovaleva, Y.A. et al. Stability of nickel(II) glycylglycinate complexes in aqueous solutions of dimethylsulfoxide at 298.15 K. Russ. J. Phys. Chem. 87, 1135–1137 (2013). https://doi.org/10.1134/S0036024413070224
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DOI: https://doi.org/10.1134/S0036024413070224