This work presents a detailed study of the coordination of Eu(III) with tartrate and oxalate ligands in aqueous solutions. The following techniques were employed: potentiometric titrations, 1D 1H, 13C multinuclear NMR spectroscopy, 2D NMR experiments (COSY, HMQC, HMBC), and UV-Vis spectroscopy. Overall (cumulative) formation constants (logβ) were determined at ionic strengths of 0.1, 0.5, and 1.0, M KNO3 over the temperature range 298–318 K. At 298 K, the oxalate complexes are significantly more stable (logβ = 7.63→15.70 as the ionic strength increases from 0.1 to 1.0 M) than the corresponding tartrate species (logβ = 5.11→8.87). Analysis of the temperature dependence of logβ shows that the Gibbs free energy change comprises both temperature-dependent terms and an approximately temperature-independent covalent contribution, the latter becoming strongly negative values in the tartrate system. The NMR data support a bidentate coordination mode involving deprotonated hydroxyl and carboxylate groups, whereas 17O NMR monitors the mechanism of water exchange within the Eu(III) hydration sphere. In the UV-Vis domain, a distinct blue shift in the absorption band is observed at 0.1 M KNO3, while at 1.0 M KNO3, the band shows a pronounced decrease in intensity, a hypochromic effect. This behavior can be attributed to increased structural distortion and a partial loss of coplanarity within the tartrate coordination environment. By contrast, the oxalate system behaves differently: the spectra, together with the thermodynamic data, support a more covalent Eu–O interaction, consistent with stabilization of Eu(III) by two dicarboxylate ligands adopting distinct coordination modes.
Issabekova et al. (Mon,) studied this question.