BINDING ABILITY OF N-PARA-AMINO-PHENYLSULFONYL DERIVATIVES OF AMINO-ACIDS - POTENTIOMETRIC AND SPECTROSCOPIC STUDIES OF CU(II) COMPLEXES

Citation
T. Kowalikjankowska et al., BINDING ABILITY OF N-PARA-AMINO-PHENYLSULFONYL DERIVATIVES OF AMINO-ACIDS - POTENTIOMETRIC AND SPECTROSCOPIC STUDIES OF CU(II) COMPLEXES, Journal of inorganic biochemistry, 57(3), 1995, pp. 183-190
Citations number
19
Categorie Soggetti
Biology,"Chemistry Inorganic & Nuclear
ISSN journal
01620134
Volume
57
Issue
3
Year of publication
1995
Pages
183 - 190
Database
ISI
SICI code
0162-0134(1995)57:3<183:BAONDO>2.0.ZU;2-8
Abstract
N-Para-amino-phenylsulfonyl derivatives of amino acids are very effect ive ligands for Cu(II) ions. Potentiometric and spectroscopic results have shown that Cu(II) ions are able to deprotonate and bind to sulfon amide nitrogen below pH 5 to form stable mono- and bis-{N-, COO-} chel ates. The basicity of sulfonamide nitrogen is lower than peptide amide nitrogen and no distinct anchoring site is necessary to promote the a mide nitrogen deprotonation.