| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5389729 | Chemical Physics Letters | 2006 | 7 Pages |
Abstract
Styrene oxide (SO), on photo-excitation at 193Â nm, undergoes molecular re-arrangement to generate enolic forms of phenylacetaldehyde and acetophenone, which subsequently either undergo cleavage of COH bond to produce OH, or get stabilized to corresponding keto forms.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Awadhesh Kumar, Sumana SenGupta, K.K. Pushpa, P.D. Naik, P.N. Bajaj,