Cycloelimination reactions of cyclic aryl pinacol sulfites and carbonates via photosensitized reversible electron transfer

Nicholas J. Turro, Chen Ho Tung, Ian Gould, Gary W. Griffin, R. L. Smith, A. Manmade

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Evidence is presented that the singlet and triplet photosensitized cycloelimination reactions of cyclic aryl pinacol sulfites and carbonates proceed by reversible electron transfer and yield products which are different from those formed on direct photolysis.

Original languageEnglish (US)
Pages (from-to)265-270
Number of pages6
JournalJournal of Photochemistry
Volume24
Issue number3
DOIs
StatePublished - 1984
Externally publishedYes

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Sulfites
Carbonates
Photolysis
Electrons

Cite this

Cycloelimination reactions of cyclic aryl pinacol sulfites and carbonates via photosensitized reversible electron transfer. / Turro, Nicholas J.; Tung, Chen Ho; Gould, Ian; Griffin, Gary W.; Smith, R. L.; Manmade, A.

In: Journal of Photochemistry, Vol. 24, No. 3, 1984, p. 265-270.

Research output: Contribution to journalArticle

Turro, Nicholas J. ; Tung, Chen Ho ; Gould, Ian ; Griffin, Gary W. ; Smith, R. L. ; Manmade, A. / Cycloelimination reactions of cyclic aryl pinacol sulfites and carbonates via photosensitized reversible electron transfer. In: Journal of Photochemistry. 1984 ; Vol. 24, No. 3. pp. 265-270.
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AU - Smith, R. L.

AU - Manmade, A.

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