The photolysis of several alkanophenones in monovalent cation exchanged faujasites and in pentasil zeolites, occured with expected γ-hydrogen abstraction and the ratio of the products derived differed; cyclobutanol formation was completely suppressed in pentasils, probably due to restruction of the rotational motion of the central σ bond present in the Norrish type II derived 1,4-diradical.
|Original language||English (US)|
|Number of pages||2|
|Journal||Journal of the Chemical Society, Chemical Communications|
|State||Published - Jan 1 1989|
ASJC Scopus subject areas
- Molecular Medicine