SPIN TRAPPING BY USE OF N-TERT-BUTYLHYDROXYLAMINE - INVOLVEMENT OF FENTON REACTIONS

被引:6
作者
LAGERCRANTZ, C
机构
[1] Department of Medical Physics, University of Göteborg, S-400 33 Göteborg
来源
FREE RADICAL RESEARCH COMMUNICATIONS | 1991年 / 14卷 / 5-6期
关键词
EPR SPECTROSCOPY; SPIN TRAPPING; FENTON REACTIONS; N-TERT-BUTYLHYDROXYLAMINE; 2-METHYL-2-NITROSOPROPANE; HYDROXYL RADICALS; HYDROGEN-PEROXIDE; SUPEROXIDE; NITROXIDE; RESONANCE; ACID; IRON;
D O I
10.3109/10715769109093428
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spin trapping of short-lived R. radicals is done by use of N-tert-butylhydroxylamine (1) and H2O2. The hydroxylamine is oxidized to the radical t-BuN(O)H (2) which is converted into the spin trap 2-methyl-2-nitrosopropane (3). Simultaneously, hydroxyl radicals. OH are formed from H2O2. The latter radical species abstracts hydrogen atoms from suitable molecules HR to give R. radicals, which are trapped with the formation of aminooxyl radicals, i. e., t-BuN(O)R (4) detectable by EPR spectroscopy. The reaction is enhanced by the presence of iron ions. The cleavage of H2O2 into. OH radicals is considered to involve both a radical-driven (t-BuN(O)H 2) and an iron-driven Fenton reaction. © 1991 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.
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页码:395 / 407
页数:13
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