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7906008 
Journal Article 
Double mediatory system involving a flavin analog and a p-benzoquinone derivative for photoinduced electrochemical oxidation of benzyl alcohol to benzaldehyde in acetonitrile 
Ishikawa, M; Okimoto, H; Morita, M; Matsuda, Y 
1996 
Yes 
Chemistry Letters
ISSN: 0366-7022
EISSN: 1348-0715 
Chemical Society of Japan 
11 
953-954 
English 
The photoinduced electrochemical oxidation of benzyl alcohol to benzaldehyde in acidic acetonitrile proceeded with practically 100% product selectivity and ca. 100% current efficiency under visible-light irradiation in the presence of riboflavin-2′,3′,4′,5′-tetraacetate (RF) as a mediator. A double mediatory system involving duroquinone as well as RF resulted in remarkable acceleration of the benzaldehyde formation with maintenance of both the high product selectivity and high current efficiency.