Energy partitioning in the photodissociation of C3H4O near 200 nm

M. E. Umstead, R. G. Shortridge, Ming-Chang Lin*

*此作品的通信作者

研究成果: Article同行評審

34 引文 斯高帕斯(Scopus)

摘要

The photodissociation of methylketene and acrolein near 200 nm has been investigated using a CO laser probing and conventional gas analysis methods. The dissociation of methylketene in a Vycor tube (λ ≃226 nm) produces CO with a Boltzmann vibrational temperature of about 2300 K and with an average vibrational energy of 2.0 ± 0.2 kcal/mol. These results are consistent with the mechanism proposed by Kistiakowsky and co-workers in which the ethylidene diradical is formed in the first step of the reaction CH3CHCO + hv → CH3CH (→ C2H4 ) + CO and subsequently isomerizes to ethylene. The CO was found to have a vibrational energy distribution similar to that found previously in the O(3P) + CH3C2H reaction which is believed to occur via a methylketene intermediate. The dissociation of both methylketene and acrolein below 220 nm produced CO with similar, but nonstatistical vibrational energy distributions. A mechanism involving H-atom migration in both systems is postulated in which the direct production of C2H4 + CO takes place in addition to the major, but less exothermic CH3CH + CO channel.

原文English
頁(從 - 到)1455-1460
頁數6
期刊Journal of physical chemistry
82
發行號13
DOIs
出版狀態Published - 1 1月 1978

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