1981
DOI: 10.1515/znb-1981-0609
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Lanthanide(III) Complexes of Oxamic Acid

Abstract: Abstract The preparation, for the first time, of the deprotonated complexes of oxamic acid with Ce(III), Pr(III), Nd(III), Sm(III), Eu(III), Dy(III), Ho(III) and Yb(III) is reported. Properties, analytical results, conductometric measurements, magnetic moments and spectral data (IR and diffuse reflectance spectra) are discussed in terms of possible structural types and the nature of the bonding. Oxamic acid acts as a bidentate non-bridging ligand.

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Cited by 20 publications
(2 citation statements)
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“…anticancer or antibacterial activity) and coordination flexibility of carboxylate or oxamate derivatives thus motivated the preparation of the novel zinc(II) mixedligand complex containing N- (2,6-dimethylphenyl)oxamate (Hpma -) and 1,10-phenanthroline, as well as its characterisation by elemental microanalysis, FT-IR, NMR, UV-Vis spectroscopy and single-crystal X-ray diffraction. The oxamate derived ligand can have diverse chelating properties with transition or f-block metals, with potential to coordinate monodentately, bidentately (O,Oor N,O-donor), tridentately (N,O,O-or O,O,O-donor) or by adopting bridging modes in monoanionic or dianionic form [5][6][7][8][9]. The monoanionic or dianionic ligands are due to the ionisability of the carboxylic and amide protons, enabling preparation of dinuclear or polynuclear complexes [9].…”
Section: Introductionmentioning
confidence: 99%
“…anticancer or antibacterial activity) and coordination flexibility of carboxylate or oxamate derivatives thus motivated the preparation of the novel zinc(II) mixedligand complex containing N- (2,6-dimethylphenyl)oxamate (Hpma -) and 1,10-phenanthroline, as well as its characterisation by elemental microanalysis, FT-IR, NMR, UV-Vis spectroscopy and single-crystal X-ray diffraction. The oxamate derived ligand can have diverse chelating properties with transition or f-block metals, with potential to coordinate monodentately, bidentately (O,Oor N,O-donor), tridentately (N,O,O-or O,O,O-donor) or by adopting bridging modes in monoanionic or dianionic form [5][6][7][8][9]. The monoanionic or dianionic ligands are due to the ionisability of the carboxylic and amide protons, enabling preparation of dinuclear or polynuclear complexes [9].…”
Section: Introductionmentioning
confidence: 99%
“…Likewise, the coordination chemistry of oxamic acid received limited attention. It is mostly focused on the coordination modes (through carboxylate or amide groups) and spectroscopic data; for examples of transition metal’s complexes, see refs ; for lanthanide’s complexes, see refs .…”
Section: Introductionmentioning
confidence: 99%