Investigation of the mechanism of ozonolysis of (Z)-3-methyl-2-pentene using matrix isolation infrared spectroscopy

被引:10
|
作者
Coleman, Bridgett E. [1 ]
Ault, Bruce S. [1 ]
机构
[1] Univ Cincinnati, Dept Chem, Cincinnati, OH 45221 USA
基金
美国国家科学基金会;
关键词
Matrix isolation; Infrared spectroscopy; Theoretical calculations; Ozonolysis; Photochemistry; GAS-PHASE REACTIONS; SECONDARY OZONIDES; PHOTOCHEMICAL-REACTIONS; ORGANIC-COMPOUNDS; OZONE; SPECTRA; ETHYLENE; KINETICS; ETHENE; ARGON;
D O I
10.1016/j.molstruc.2012.07.046
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
The matrix isolation technique, combined with infrared spectroscopy and twin jet codeposition, has been used to characterize intermediates and stable "late" products formed during the ozonolysis of (Z)-3-methyl-2-pentene (MP). While twin jet deposition led to minimal product formation, annealing to 35 K produced a number of product bands. Based on isotopic labeling and theoretical calculations, product bands have been assigned to the primary ozonide and also tentatively to the secondary ozonide of MP. Indirect evidence for formation of one or both possible Criegee intermediates in this system is presented. While neither possible Criegee intermediate for this system was observed, the evidence overall clearly supports the mechanism first proposed by Criegee for the ozonolysis of alkenes. UV irradiation led to product arising from O atom addition to MP, while merged jet codeposition led to a number of stable products for this system. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 143
页数:6
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