Free Radicals in Pyrimidines: ESR of γ-Irradiated 5-Cyclohexenyl-1,5-Dimethyl Barbituric Acid

ESR studies have determined that ionizing radiation damage of hexobarbital (5-cyclohexenyl-1,5-dimethylbarbituric acid) causes the formation of a free radical (A) by hydrogen abstraction from the cyclohexenyl group. Hyperfine coupling tensors were determined for coupling of the unpaired electron to...

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Veröffentlicht in:Radiat. Res.; (United States) 1981-06, Vol.86 (3), p.411-418
Hauptverfasser: Benson, Brent, Erich, Lester
Format: Artikel
Sprache:eng
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Zusammenfassung:ESR studies have determined that ionizing radiation damage of hexobarbital (5-cyclohexenyl-1,5-dimethylbarbituric acid) causes the formation of a free radical (A) by hydrogen abstraction from the cyclohexenyl group. Hyperfine coupling tensors were determined for coupling of the unpaired electron to four protons. Visible light of wavelengths near 450 nm reversibly converts this radical to a second free radical (B) which also has the unpaired electron localized in the cyclohexenyl group. The activation energy for a thermally induced reverse conversion (B → A) was determined to be 1.4 eV.
ISSN:0033-7587
1938-5404
DOI:10.2307/3575457