TY - JOUR
T1 - Reactions of low valent transition metal complexes with hydrogen peroxide. Are they "fenton-like" or not? 4. The case of fe(II)l, l = edta; hedta and tcma
AU - Luzzatto, Esther
AU - Cohen, Haim
AU - Stockheim, Claudia
AU - Wieghardt, Karl
AU - Meyerstein, Dan
N1 - Funding Information:
We wish to thank Y. Nahon, D. Carmi, S. Cohen and Y. Nehemia for technical assistance. This study was supported by the German-Israeli Binational Science Foundation, Jerusalem, and the Israeli Atomic Energy Commission. D.M. wishes to express his thanks to Mrs. Irene Evans for continuous interest and support.
PY - 1995
Y1 - 1995
N2 - The question whether hydroxyl free radicals are formed in the reactions of divalent iron complexes Fe(II)L; L = edta; hedta; tcma (tcma = l-acetato-l,4,7-triazacyclononane) with hydrogen peroxide in neutral and slightly acidic solutions was studied by using the β elimination reaction as an assay for the formation of hydroxyl free radicals, OH. The results show that at pH<5.5 the iron(II)peroxide intermediate complex decomposes rapidly to yield free hydroxyl radicals for L=edta and hedta. This is in contrast to the mechanism of the corresponding Fe(II)nta peroxide complex, which probably decomposes to form Fe(IV)nta which then reacts with organic substrates to yield aliphatic free radicals. Thus, the non-participating ligand L has an appreciable effect on the mechanism of reaction of the metal center with hydrogen peroxide. Blank experiments using ionizing radiation as the source of CH2CR(CH3)OH, R = H or CH3 radicals indicate that when L = tcma intermediates of the type LFeIII-CH2CR(CH3)OHaq are formed, but their major mode of decomposition is not the β elimination reaction. Thus, the present assay for the formation of hydroxyl free radicals by the Fenton Reaction does not fit the latter system.
AB - The question whether hydroxyl free radicals are formed in the reactions of divalent iron complexes Fe(II)L; L = edta; hedta; tcma (tcma = l-acetato-l,4,7-triazacyclononane) with hydrogen peroxide in neutral and slightly acidic solutions was studied by using the β elimination reaction as an assay for the formation of hydroxyl free radicals, OH. The results show that at pH<5.5 the iron(II)peroxide intermediate complex decomposes rapidly to yield free hydroxyl radicals for L=edta and hedta. This is in contrast to the mechanism of the corresponding Fe(II)nta peroxide complex, which probably decomposes to form Fe(IV)nta which then reacts with organic substrates to yield aliphatic free radicals. Thus, the non-participating ligand L has an appreciable effect on the mechanism of reaction of the metal center with hydrogen peroxide. Blank experiments using ionizing radiation as the source of CH2CR(CH3)OH, R = H or CH3 radicals indicate that when L = tcma intermediates of the type LFeIII-CH2CR(CH3)OHaq are formed, but their major mode of decomposition is not the β elimination reaction. Thus, the present assay for the formation of hydroxyl free radicals by the Fenton Reaction does not fit the latter system.
KW - Fe(II)(edta)
KW - Fe(II)(hedta)
KW - Fenton
KW - Hydroxyl free radicals
UR - http://www.scopus.com/inward/record.url?scp=0029411740&partnerID=8YFLogxK
U2 - 10.3109/10715769509065266
DO - 10.3109/10715769509065266
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C2 - 7581828
AN - SCOPUS:0029411740
SN - 1071-5762
VL - 23
SP - 453
EP - 463
JO - Free Radical Research
JF - Free Radical Research
IS - 5
ER -