Temperature dependences of the rate constants and branching ratios for the reactions of OH-(H2O)(0-4)+CH3Br

被引:59
作者
Viggiano, AA
Arnold, ST
Morris, RA
Ahrens, AF
Hierl, PM
机构
[1] Phillips Laboratory, Geophysics Directorate, Ionospheric Effects Division (GPID), Hanscom AFB, MA 01731-3010
[2] House Office Building, Washington, DC 20515
[3] Topeka High School, Topeka
[4] Department of Chemistry, University of Kansas, Lawrence
关键词
D O I
10.1021/jp961250y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Various effects of solvation, isotopic substitution, and temperature on the reactions of OH-(H2O)(n=0-4) with CH3Br are reported. Increasing solvation is found to decrease reactivity dramatically as has been observed previously. For n = 0 the rate constant is large, and the temperature dependence is small, T--0.58; Br- is the only product. For n = 1 the rate constant is about a factor of 1.5 smaller than that for the n = 0 reaction, and the temperature dependence is T--1.6. This reaction produces about 90% Br- and 10% Br-(H2O), with this ratio roughly independent of temperature. The rate constant for the n = 2 reaction is almost 2 orders of magnitude lower than that fur n = 1. The n = 2 reaction is complicated in that the low-temperature behavior depends on the identity of the buffer gas. In a He buffer at all temperatures, only Br- and Br-(H2O) products are observed, while in a H-2 buffer another product, OH(H2O)(2)CH3Br-, is observed at low temperatures in addition to the above products. The temperature dependence of this reaction is flat in a He buffer over the entire experimental temperature range and in a H-2 buffer in the range 300 K and above. The temperature dependence in a H-2 buffer is about T-4 for temperatures below 300 K. The n = 3 reaction is about a factor of 10 slower than the n = 2 reaction at 163 K and proceeds entirely by association. For n = 4 an upper limit for the rate constant of k less than or equal to 2 x 10(-13) cm(3) s(-1) is found at 163 K. For the reaction of OH-(H2O) with CH3Br eight isotopic variants were studied: OH-(H2O) with 0-3 deuterium atoms and both CH3Br and CD3Br. No isotopic effect was found between CD3Br and CH3Br. For OH-(H2O) isotopic substitution, the reactivity order was H2DO2- greater than or equal to HD2O2- > H3O2- greater than or equal to D3O2-. The ions group into two categories: those incorporating both hydrogen and deuterium and those with only hydrogen or deuterium. The former group was found to react about 10% more rapidly than the latter group.
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页码:14397 / 14402
页数:6
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