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Studies on the Redox Characteristics of Ferrioxamine E

Thermodynamic parameters for the reduction of ferrioxamine E as calculated from redox potentials determined at four different temperatures were found to be ΔH≠=7.1±3.4 kJ mol−1 and ΔS≠=−146 J mol−1 K−1. The negative entropy value is large, because the decrease in the charge at the metal center and a...

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Published in:Chemistry & biodiversity 2010-03, Vol.7 (3), p.656-665
Main Authors: Kazmi, S. Arif, Shorter, A. Lee, McArdle, James V., Ashiq, Uzma, Jamal, Rifat Ara
Format: Article
Language:English
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Summary:Thermodynamic parameters for the reduction of ferrioxamine E as calculated from redox potentials determined at four different temperatures were found to be ΔH≠=7.1±3.4 kJ mol−1 and ΔS≠=−146 J mol−1 K−1. The negative entropy value is large, because the decrease in the charge at the metal center and an increase in its ionic radius force the structure of the complex to become less rigid and resemble the desferrisiderophore. The hydrophilic groups of the system are now (relatively more) available for solvent interaction. Thus, a large negative entropy change accompanies the reduction of the complex. Kinetics of reduction of ferrioxamine by VII, CrII, EuII, and dithionite were measured at different temperatures and by dithionite at different pH values. The CrII and EuII reactions proceed by an inner‐sphere mechanism and have second‐order rate constants at 25° of 1.37×104 and 1.23×105 M−1 s−1, respectively. For the VII reduction, the corresponding rate constant was 1.89×103 M−1 s−1. The activation parameters for the VII reduction were ΔH≠ = 8.3 kJ mol−1; ΔS≠ =−154 J mol−1 K−1. These values are indicative of an outer‐sphere mechanism for VII reduction. The reduction by dithionite is half order in dithionite concentration indicating that SO$\rm{{_{2}^{-}}}$. is the sole reducing species. log of reduction rate constants of different trihydroxamates by this reductant were correlated with their respective redox potentials, and the variation was found to be in approximate correspondence with the expectations of Marcus relationship.
ISSN:1612-1872
1612-1880
DOI:10.1002/cbdv.200900031