Reaction of hydrogen peroxide with low molecular weight iron complexes

• Published in: International journal of radiation applications and instrumentation. Part C, Radiation physics and chemistry Vol. 32; no. 1; pp. 129 - 135
• Main Authors: Rahhal, Siham, Richter, Helen W.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 1988
• ISSN: 1359-0197; 1878-1020
• DOI: 10.1016/1359-0197(88)90026-4

Fe(II) complexed with trans-1,2-diaminocyclohexane- N,N,N',N'-tetraacetic acid (CDTA) reacts with hydrogen peroxide in neutral aqueous solution at room temperature to yield reactive species which are not scavenged by t-butanol, under conditions where >90% of hydroxyl radical would be scavenged. Further, the ratio of the rate constants for the reaction of the reactive species with Fe(II)CDTA and H 2O 2 is 6.2, in contrast to a ratio of 200 which would result if the species were the hydroxyl radical. Thus, it is concluded that the reactive species produced is not the hydroxyl radical, but an iron-oxo species such as the ferryl ion. The reactive species is formed in an apparent first order reaction, when either hydrogen peroxide or Fe(II)CDTA is in kinetic excess. The bimolecular reaction rate constant is (1.26 ± 0.19) × 10 3 M -1 s -1. In experiments where H 2O 2 was in kinetic excess, a chain decomposition of H 2O 2 was observed in which the initially produced iron-oxo intermediate exhibits hydroperoxidase activity.