Interaction between iron(II) and hydroxamic acids:: oxidation of iron(II) to iron(III) by desferrioxamine B under anaerobic conditions

被引:67
作者
Farkas, E [1 ]
Enyedy, ÉA
Zékány, L
Deák, G
机构
[1] Univ Debrecen, Dept Inorgan & Analyt Chem, H-4010 Debrecen, Hungary
[2] Univ Debrecen, Dept Appl Chem, H-4010 Debrecen, Hungary
基金
匈牙利科学研究基金会;
关键词
desferrioxamine B; hydroxamic acid; Fe(II)/Fe(III); anaerobic oxidation; complex;
D O I
10.1016/S0162-0134(00)00197-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interaction between iron(II) and acetohydroxamic acid (Aha), alpha -alaninehydroxamic acid (alpha -Alaha), beta -alaninehydroxamic acid (beta -Alaha), hexanedioic acid bis(3-hydroxycarbamoyl-methyl)amide (Dha) or desferrioxamine B (DFB) under anaerobic conditions was studied by pH-metric and UV-Visible spectrophotometric methods. The stability constants of complexes formed with Aha, alpha -Alaha, beta -Alaha and Dha were calculated and turned out to be much lower than those of the corresponding iron(III) complexes. Stability constants of the iron(II)-hydroxamate complexes are compared with those of other divalent id-block metal ions and the Irving-Williams series of stabilities was found to be observed. Above pH 4, in the reactions between iron(II) and desferrioxamine B, the oxidation of the metal ion to iron(III) by the ligand was found. The overall reaction that resulted in the formation of the tris-hydroxamato complex [Fe(HDFB)](+) and monoamide derivative of DFB at pH 6 is: 2Fe(2+) + 3H(4)DFB(+) = 2[Fe(HDFB)](+) + H3DFB-monoamide(+) + H2O + 4H(+) Based on these results, the conclusion is that desferrioxamine B can uptake iron in iron(III) form under anaerobic conditions. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:107 / 114
页数:8
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