Abstract
2-Phenylethyl radicals
(Ph-CH2-�CH2) were prepared by the decarboxylation
reaction of 3-phenylpropanoic acid with sulfate radical ions (SO4-�)
formed during the pulse radiolysis of aqueous solutions containing
peroxydisulfate (S2O82-) ions. The ultraviolet
absorption spectrum of the transient radicals consisted of a band centred at
309nm with an extinction coefficient of 5000 1, mol-1 cm-1.
Attempts were made to form phenylethyl radicals by the electron-attachment
dissociation reaction of (2-haloethy1)benzenes. Contrary to literature reports,
it was found that the latter reaction does not occur in either cyclohexane,
benzene or aqueous solutions of (2-chloroethyl)- and (2-bromoethyl)-benzenes.
Cited by
4 articles.
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