Comparison of spectral and thermal properties and antibacterial activity of new binary and ternary complexes of Sm(III), Eu(III) and Gd(III) ions with N-phenylanthranilic acid and 1,10-phenanthroline
التفاصيل البيبلوغرافية
العنوان:
Comparison of spectral and thermal properties and antibacterial activity of new binary and ternary complexes of Sm(III), Eu(III) and Gd(III) ions with N-phenylanthranilic acid and 1,10-phenanthroline
New binuclear binary and ternary complexes of Sm(III), Eu(III), and Gd(III) ions with N-phenylanthranilic acid and 1,10-phenanthroline were obtained in solid phase and characterized by chemical and elemental analysis, molar conductance, UV–vis and IR spectroscopies as well as thermoanalytical techniques (TG/DTG–DSC coupled with MS and FT-IR). The dilution method was used to examine the antibacterial activity of the synthesized compounds. The spectroscopic studies indicated that the carboxylate group of N-phenylantranilate ligand is involved in the coordination of metal ion both in binary and ternary complexes. Thermal decomposition of the obtained compounds was carried out in air and nitrogen atmosphere. During heating the complexes decompose via intermediate products to the oxide (Ln2O3) in air atmosphere and to the oxide (Ln2O3) or oxide polluted by carbon (Ln2O3+nC) in nitrogen atmosphere. The dehydration process was discussed in relation to the nature of water present in these compounds. Using coupled TG-FTIR-MS techniques the decomposition pathways of the synthesized compounds were examined. Additionally, gaseous products released during pyrolysis and thermal oxidation of the complexes were identified. All the complexes exhibit marked activity against two Gram-negative (Escherichia coli and Pseudomonas aeruginosa) and one Gram-positive (Staphylococcus aureus) bacterial strains. The ternary complexes, especially Gd(III) complex in comparison with the binary ones, have enhanced activity against Escherichia coli. Moreover, antibacterial activity of the synthesized compounds with respect to Pseudomonas aeruginosa is comparable to tetracycline and greater than for kanamycin, erythromycin, and ampicillin.