Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1887392 | Radiation Physics and Chemistry | 2007 | 6 Pages |
Abstract
The radical cation of (phenoxymethyl)oxirane (PGEâ
+) is generated by pulse radiolysis in dichloromethane solution and by direct action of radiation on the title compound. In the pure system its UV-vis spectrum is characterized by two bands at 340 and 430Â nm, such that the electronic structure corresponds to a dipole bearing the positive charge on the phenoxy side. At the same time, the phenoxy-oxirane bridge is weakened. Then, the radical cation fragments into a phenoxonium ion and an oxyranylmethyl radical (kPGE-fragm=1.16Ã107s-1). The latter immediately rearranges to an allyloxyl radical by ring opening. It is then conceived that the action of onium salts, as radiation curing initiators of phenoxy-oxirane derivatives, occurs after epoxy ring opening.
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Authors
Salvatore S. Emmi, Ugo Corda, Piergiorgio Fuochi, Marco Lavalle, Sabina Alessi, Giuseppe Spadaro,