Equilibrium Study of Mixed Complexes of Uranyl Ion with Pyridine Carboxylic Acids as Primary and Some Dicarboxylic Acids as Secondary Ligands
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Description
Department of Chemistry, Marathwada University, Aurangabad-431 004
Department of Chemistry, Georgia State University, University Plaza, Atlanta, Georgia-30302, U. S. A.
Manuscript received 20 February 1979, accepted 6 October 1979
Equlibrium constants of the binary and ternary complexes of UO\(_2^{3+}\) with pyridine carboxylic acids and some dicarboxylic acids have been investigated by \(p\)H titration method at 30° and µ =0.1 M (NaClO4). Pyridine carboxylic acids used are picolinic, quinolinic, dipicolinic and dicarboxylic acids are malic, maleic, chlorosuccinic, dimercapto succinic, methylmalonic and dimethylmaionic, UO\(_2^{2+}\), forms 1 : 1 and 1: 2 binary bis complexes with all the ligand acids except maleic, chlorosuccink and dimercapto succinic.
Ternary chelates of UO\(_2^{2+}\) pyridine carboxylic-secondary acid systems have been studied. Binary stabilities are explained on the ring size effect and nature of substituent in the parent acids. Equilibrium constants of ternary complexes were utilized to discuss the preferential formation of ternary complexes over binary. The values of K2\(YX\) and \(\beta\)\(XY\) depend on the basicities of the secondary ligands and 1 : 1 binary stabilities of the metal chelates respectively.
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