Self- and cross-reactions of β-hydroxyperoxy radicals of relevance to tropospheric monoterpene oxidation:: structure-activity relationships for rate coefficients

被引:15
作者
Boyd, AA [1 ]
Villenave, E [1 ]
Lesclaux, R [1 ]
机构
[1] Univ Bordeaux 1, CNRS, Lab Phys Chim Mol, F-33405 Talence, France
关键词
peroxy radicals; terpenes; kinetics; structure activity relationships; cyclohexene;
D O I
10.1016/S1352-2310(03)00253-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The laser flash photolysis technique has been used to measure rate coefficients for the self- and cross-reactions of four peroxy radicals, which have been selected as surrogate of those peroxy radicals resulting from the OH addition to monoterpenes: the 2-hydroxycyclohexylperoxy c-C6H10(OH)O-2 (I), 2-hydroxy-1,2-dimethylcyclohexylperoxy c-C6H8(CH3)(2)(OH)O-2 (II), 2-hydroxy-2-methyleyclohexylperoxy c-C6H9(OH)CH3O2 (III) and 2-hydroxy-1-methylcyclohexylperoxy c-C6H9CH3(OH)O-2 (IV) radicals. Those radicals were obtained by addition of OH and O-2 to cyclohexene and 1,2-dimethylcyclohexene for I and II, respectively, and to 1-methylcyclohexene for (III) and (IV). Rate constants for self-reactions of radicals I and II are: k(8) = (1.60 +/- 0.10) x 10(-12) and k(12) = (2.00 +/- 0.05) x 10(-14) (units of cm(3) molecule(-1) s(- 1), errors 2sigma) at 298degreesK and in 1 atm air. Assuming that both the secondary radicals I and III and both the tertiary radicals 11 and IV have similar self-reaction rate constants, the rate constant for cross-reaction (13) between III and IV has been determined: k(13) = (6.15 +/- 0.33) x 10(-13) cm(3) molecule(-1) s(-1). The self-reaction rate constant of the peroxy radical c-C6H8(OH)O-2, formed by OH and O-2 addition to 1,4-cyclohexadiene, was also estimated and found to be of same order of magnitude as k8, thus showing that the non-conjugated double bond in the radical has no significant effect on the rate constant. Structure-activity relationships are discussed, particularly for self- and cross-reactions involving secondary and tertiary peroxy radicals, in view of their relevance to tropospheric oxidation modelling of alkenes and monoterpenes. In particular, emphasis is given to the large increase in reactivity resulting from the beta-OH substitution, compared to non-substituted species. As part of this work, a rate constant of (1.5 +/- 0.5) x 10(-14) cm(3) molecule(-1) s(-1) was measured for the self-reaction of the beta-OH substituted t-butylperoxy radical (CH3)(2)C(O-2)CH2OH. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2751 / 2760
页数:10
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