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Trozzola, A.M., Yager, W.A., Griffin, G.W., Kristinsson, H. and Sarkar, I. (1967) Direct Evidence for the Formation of Diphenylmethylene in the Photolysis of Triphenyl- and Tetra-phenyloxirane. Journal of the American Chemical Society, 89, 3357-3358.
https://doi.org/10.1021/ja00989a051

has been cited by the following article:

• TITLE: Photochemistry of Styrene Oxide: A Triplet Pathway in the Singlet Excitation of a Monoaryl Oxirane

  AUTHORS: Benny E. Aney, Heiko Ihmels, Rick C. White

  KEYWORDS: Photochemistry, Oxiranes, Cyclic Carbonate Esters, Mechanisms

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.7 No.3, September 1, 2017

  ABSTRACT: Direct photolysis and quenching experiments with styrene oxide support the existence of an efficient triplet photochemical pathway to benzyl radical formation. Similar photolytic behavior for styrene glycol carbonate strongly supports the 1,3-diradical, resulting from the scission of the benzylic C-O bond, as the geometric source of the triplet pathway. Primary photoproducts were determined by both NMR and HPLC analysis and we observed that toluene and bibenzyl were both primary photoproducts, not secondary photoproducts.