Investigation of the Thermal and Photochemical Reactions of Ozone with 2,3-Dimethyl-2-butene

被引:12
|
作者
Coleman, Bridgett E. [1 ]
Ault, Bruce S. [1 ]
机构
[1] Univ Cincinnati, Dept Chem, Cincinnati, OH 45221 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2010年 / 114卷 / 48期
基金
美国国家科学基金会;
关键词
GAS-PHASE REACTION; INFRARED MATRIX-ISOLATION; SECONDARY OZONIDES; SOLID ARGON; SPECTRA; ETHYLENE; OZONOLYSIS; KINETICS; MECHANISM; PRODUCTS;
D O I
10.1021/jp108457w
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 formed during the ozonolysis of 2,3-dimethy1-2-butene (DMB). Absorptions of early intermediates in the twin jet experiments grew up to 200% upon annealing to 35 K. A number of these absorptions have been assigned to the elusive Criegee intermediate (CI) and secondary ozonide (SOZ) of DMB, transient species not previously observed for this system. Also observed was the primary ozonide (POZ), in agreement with earlier studies. The wavelength dependence of the photodestruction of these product bands was explored with irradiation from lambda >= 220 to >= 580 nm. Merged jet (flow reactor) experiments generated "late" stable oxidation products of DMB. A recently developed concentric jet method was also utilized to increase yields and monitor the concentration of intermediates and products formed at different times by varying the length of mixing distance (d = 0 to -11 cm) before reaching the cold cell for spectroscopic detection. Identification of intermediates formed during the ozonolysis of DMB was further supported by O-18 and scrambled O-6,O-18 isotopic labeling experiments as well as theoretical density functional calculations at the B3LYP/6-31++G(d,2p) level.
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页码:12667 / 12674
页数:8
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