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High Pressure Photochemistry of Alkenes. 6. the Case of 1-Methylcyclopentene At 184.9 and 147.0 nm

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The degradation of the 184.9 nm photoexcited 1-methyl-1-cyclopentene molecule shows the involvement of various excited isomers. The most important fragmentation products are 1- and 2-methyl-1,9-cyclopentadiene. These products are probably the result of a one-step elimination process of a hydrogen molecule. This process has also been observed in the case of the 184.9 nm photochemistry of cyclopentene. On the other hand, the involvement of isomers, although possible, is not so obvious at 147.0 nm. Moreover, in this case, the 1- and 2-methyl-1,9-cyclopentadiene formation is the result of hydrogen atom elimination in a two-step process. Cyclopentadiene, ethylene, and various C3 and C4 compounds are formed as well as methyl radicals and hydrogen atoms. These products are probably formed in successive elimination reactions as this is also observed in acyclic alkenes.

Affiliations: 1: Département des sciences fondamentales Université du Québec à Chicoutimi Chicoutimi, Québec G7H 2B1

10.1163/156856789X00140
/content/journals/10.1163/156856789x00140
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/content/journals/10.1163/156856789x00140
1989-01-01
2016-12-08

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