Radical additions of xenon difluoride to cis- and trans-1-phenylpropenes: comparison with trichloramine and iodobenzene dichloride

Abstract

We would like to report data which support a free radical pathway for reaction of xenon difluoride (XeF 2) with alkenes in organic solvent. Radical intermediates have been proposed for reaction of XeF 2 to double bonds. For example, a radical pathway was suggested for the gas phase reaction of XeF 2 to ethylene and propene [1]. Zupan speculated on a radical cation pathway for the acid catalyzed reaction of XeF 2 with alkenes but gave no experimental evidence for this mechanism [2,3]. Radical cation intermediates were demonstrated for the reaction of XeF 2 to aromatics by Filler [4]. Acid catalyzed ionic reactions to unsaturated hydrocarbons have been reviewed [5]. Zupan and Pollak have shown that alkenes do not react in aprotic solvent with XeF 2 at low concentrations of alkene unless acid catalyst is present [3]. However, we observed that illumination of a dilute solution of cis- or trans -1-phenylpropenes (I) or (II) in methylene chloride at 0° with a 270 watt sunlamp produced IIIa and IIIb in less then two hours (Table). Furthermore, at high concentration of (I) and (II), a spontaneous reaction occurred in the dark between XeF 2 and these styrenes. The reaction conditions for both of these reactions imply a radical mechanism — the latter a molecule-induced pathway.