Direct observation of the gas-phase Criegee intermediate (CH2OO)

被引:182
作者
Taatjes, Craig A. [1 ]
Meloni, Giovanni [1 ]
Selby, Talitha M. [1 ]
Trevitt, Adam J. [2 ,3 ]
Osborn, David L. [1 ]
Percival, Carl J. [4 ]
Shallcross, Dudley E. [5 ]
机构
[1] Sandia Natl Labs, Combust Res Facil, Mail Stop 9055, Livermore, CA 94551 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Ernest Orlando Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[4] Univ Manchester, Sch Earth Atmospher & Environm Sci, Manchester M13 9PL, Lancs, England
[5] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
基金
英国自然环境研究理事会; 美国国家航空航天局;
关键词
D O I
10.1021/ja804165q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbonyl oxide species play a key role in tropospheric oxidation of organic molecules and in low-temperature combustion processes. In the late 1940s, Criegee first postulated the participation of carbonyl oxides, now often called "Criegee intermediates," in ozonolysis of alkenes. However, despite decades of effort, no gas phase Criegee intermediate has before been observed. As a result, knowledge of gas phase carbonyl oxide reactions has heretofore been inferred by indirect means, with derived rate coefficients spanning orders of magnitude. We have directly detected the primary Criegee intermediate, formaldehyde oxide (CH2OO), in the chlorine-initiated gas-phase oxidation of dimethyl sulfoxide (DMSO). This work not only establishes that the Criegee intermediate is formed in DMSO oxidation also but opens the possibility for explicit kinetics studies on this critical atmospheric species. Copyright © 2008 American Chemical Society.
引用
收藏
页码:11883 / 11885
页数:3
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