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 language | English (US) |
|---|---|
| Pages (from-to) | 265-270 |
| Number of pages | 6 |
| Journal | Journal of Photochemistry |
| Volume | 24 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1984 |
| Externally published | Yes |
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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 journal › Article
}
TY - JOUR
T1 - Cycloelimination reactions of cyclic aryl pinacol sulfites and carbonates via photosensitized reversible electron transfer
AU - Turro, Nicholas J.
AU - Tung, Chen Ho
AU - Gould, Ian
AU - Griffin, Gary W.
AU - Smith, R. L.
AU - Manmade, A.
PY - 1984
Y1 - 1984
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=33750869066&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33750869066&partnerID=8YFLogxK
U2 - 10.1016/0047-2670(84)87005-7
DO - 10.1016/0047-2670(84)87005-7
M3 - Article
VL - 24
SP - 265
EP - 270
JO - Journal of Photochemistry
JF - Journal of Photochemistry
SN - 0047-2670
IS - 3
ER -