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Photochemical reaction intermediates of benzyl chloride in condensed phase

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Reaction intermediates produced upon the photolysis of benzyl chloride have been studied in glassy matrix and in solution. In the steady-state photolysis both benzyl radicals and structural isomers of benzyl chloride were formed in ethanol, while in 3-methylpentane the structural isomers were predominantly formed. The nanosecond laser photolyses of benzyl chloride in ethanol and in cyclohexane also generated benzyl radicals and structural isomers at room temperature. In acetonitrile, in addition to these species, benzyl cations were observed in the early stage after the photolysis.

Affiliations: 1: Department of Chemistry, Gunma University, Kiryu Gunma 376-8515, Japan; 2: Takasaki Radiation Chemistry Research Establishment, Japan Atomic Energy Research Institute, 1233 Watanuki,Takasaki,Gunma 370-1292, Japan; 3: Department of Chemistry, Kyusyu Institute of Technology, Sensuicho, Tobata-ku, Kitakyushu Fukuoka 804-8550, Japan

10.1163/156856701745032
/content/journals/10.1163/156856701745032
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/content/journals/10.1163/156856701745032
2017-08-19

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