skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Reactions of iron porphyrins with methyl radicals

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00400a036· OSTI ID:6255298

The reactions of methyl radicals with ferric, ferrous, and iron-free-deuteroporphyrin have been investigated in neutral and alkaline water-2-propanol mixtures. Steady-state radiolysis of methyl chloride saturated solutions of ferric deuteroporphyrin, or chemical reduction of ferric deuteroporphyrin solutions containing methyl iodide, led to a new species which is spectrophotometrically characterized. The yield (G approx. = 3) and the redox titration (2 reducing equivalents) strongly suggest the structure DPFe/sup III/CH/sub 3/. This product is found to be stable under anaerobic conditions but is oxidized to the initial ferric form in the presence of air. Pulse radiolysis experiments show that methyl radicals react with both ferric and ferrous deuteroporphyrin with reaction rate constants of 2.3 x 10/sup 9/ and 3.9 x 10/sup 9/ M/sup -1/ s/sup -1/, respectively. The reaction with iron-free deuteroporphyrin is much slower, demonstrating that methyl radicals react with iron porphyrin at the iron center. The transient species resulting from the scavenging of a methyl radical by ferric porphyrin DPFe/sup IV/CH/sub 3/ undergoes a further slow reaction leading to ferrous deuteroporphyrin (t/sub 1/2/ approx. = 200 ..mu..s). Electron (or methyl) transfer between DPFe/sup IV/CHTnumber and ferrous deuteroporphyrin leading to DPFe/sup III/CH/sub 3/ and ferric deuteroporphyrin is shown to occur with a second-order rate constant k = 4 x 10/sup 8/ M/sup -1/ s/sup -1/. The reactions of ..cap alpha..-hydroxyisopropyl radicals with ferric, ferrous, and iron-free deuteroporphyrin and with methyl iodide were also studied. The reactions of methyl radicals are discussed in relation to the hypothesis of radical-mediated toxicity of halogenated compounds.

Research Organization:
Univ. of Notre Dame, IN
OSTI ID:
6255298
Journal Information:
J. Am. Chem. Soc.; (United States), Vol. 103:10
Country of Publication:
United States
Language:
English

Similar Records

One-electron reduction of ferriporphyrins and reactions of ferric and ferrous porphyrins with a halothane-derived radical. [Gamma Radiation]
Journal Article · Thu Aug 19 00:00:00 EDT 1982 · J. Phys. Chem.; (United States) · OSTI ID:6255298

One-electron reduction of iron(II) porphyrin and characterization of iron(I) porphyrin in aqueous medium. Steady-state and pulse radiolysis studies. [Gamma radiation]
Journal Article · Thu Nov 22 00:00:00 EST 1984 · J. Phys. Chem.; (United States) · OSTI ID:6255298

Reactions of iron porphyrins with CF/sub 3/, CF/sub 3/O/sub 2/, and CBr/sub 3/O/sub 2/ radicals
Journal Article · Thu Jul 16 00:00:00 EDT 1987 · J. Phys. Chem.; (United States) · OSTI ID:6255298