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2 Polish Journal of Chemistry

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Termodynamic Study of the Interaction Between Some Recently Synthesized Benzo-Substituted Macrocyclic Diamides with Some Pyridinium Ion Derivatives in Acetonitrile Solution

100%

Ganjali M. , Zargazi M. H. , Mohajeri A.

tom Vol. 75, nr 5

743-749

The formation of pyridinium, 2-methyl pyridinium, 2,4-dimethyl pyridinium and 2,4,6- trimethyl pyridinium complexes with the some recently synthesized benzo-substituted macrocyclic diamides was investigated conductometrically in acetonitrile solution at various temperatures. The formation constants of the resulting 1:1 complexes were determined from the computer fitting of the molar conductance-mole ratio data. In all cases studied, the stability of complexes decreases in the order Py+ > 2m-Py+ > 2,4dim-Py+ > 2,4,6trim-Py+. The enthalpy and entropy of complexation reaction were determined from the temperature dependence of the formation constants. In all cases, the complexes were enthalpy stabilized but entropy destabilized.

Differential Pulse Polarographic Study of Mercury Complexes with Some Substituted Pyrimidines in Binary Acetonitrile-Dimethylformamide Mixtures

88%

Maddah B. , Alizadeh K. , Shamsipur M. , Moghimi A. , Ganjali M.

2006

tom Vol. 80, nr 5

737-744

The complex formation of Hg2+ ion with five synthesized substituted pyrimidines in binary acetonitrile-dimethylformamide (AN-DMF) mixtures was studied by differential pulse polarography at 25 graduate C. The stoichiometry and stability of the complexeswere determined by monitoring the shift in the Hg2+ differential pulse peak potential against the pyrimidines concentration. In all cases studied, itwas found that the stability of the resulting 1:1 complex decreases drastically by increasing the amount of dimethylformamide in the binary mixtures. The observed stability order in a given solvent mixture is discussed in terms of the solvating ability of the solvent, donor site number, and steric hindrance on the pyrimidines.