Potentiometric and spectroscopic studies on copper(II) complexes of non-proteinogenic histidine analogues. (Articolo in rivista)

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  • Potentiometric and spectroscopic studies on copper(II) complexes of non-proteinogenic histidine analogues. (Articolo in rivista) (literal)
Anno
  • 2005-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.poly.2005.02.010 (literal)
Alternative label
  • K. Várnagy, E. Garribba, D. Sanna, I. Sóvágó, G. Micera (2005)
    Potentiometric and spectroscopic studies on copper(II) complexes of non-proteinogenic histidine analogues.
    in Polyhedron
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • K. Várnagy, E. Garribba, D. Sanna, I. Sóvágó, G. Micera (literal)
Pagina inizio
  • 799 (literal)
Pagina fine
  • 806 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.sciencedirect.com/science/article/pii/S0277538705000914 (literal)
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  • 24 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Department of Inorganic and Analytical Chemistry, University of Debrecen, P.O. Box 21, H-4010 Debrecen, Hungary Department of Chemistry, University of Sassari, Via Vienna 2, I-07100 Sassari, Italy Istituto C.N.R. di Chimica Biomolecolare, Sezione di Sassari, Trav. La Crucca 3 Reg. Baldinca, I-07040 Sassari, Italy (literal)
Titolo
  • Potentiometric and spectroscopic studies on copper(II) complexes of non-proteinogenic histidine analogues. (literal)
Abstract
  • Copper(II) complexes of the histidine analogues: ?-(2-pyridyl)-dl-alanine, ?-(2-thienyl)-dl-alanine, ?-(1,2,4-triazol-1-yl)-dl-alanine, ?-(2-thiazolyl)-dl-alanine ligands, and for comparison ?-(2-thienyl)glycine and 2-(2-aminoethyl)pyridine, were studied by potentiometric, UV-VIS, EPR and thermogravimetric techniques. The amino acid residues of the ligands were described as the main binding sites forming mono- and bis-(ligand) complexes, but the interaction between aromatic triazolyl and pyridyl nitrogen atoms and the copper(II) ion also was detected in the case of ?-(1,2,4-triazol-1-yl)-dl-alanine and ?-(2-pyridyl)-dl-alanine. The presence of heteroaromatic rings in the amino acid analogues influences the amino acid like coordination mode in the order imidazole > pyridyl ~ triazolyl > thiazolyl ~ thienyl rings. (literal)
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