The structure of telomers 5 a, b, prepared from 2,3-epoxypropyl methacrylate (2) and benzenethiol (la) or 1-dodecanethiol (lb) by UV irradiation, was studied by MS, IR, 'H and 13C NMR spectroscopy. The IR spectra of the products show that thiol addition occurs only at the double bond of monomer 2. Mono-and diadducts could be isolated by fractionation and were characterized spectroscopically together with higher telomers (10 < DP,, < 200). Coupling constants and chemical shifts were assigned for the mono-and diadducts unambiguously. The tacticity of higher telomers was determined and found to follow the Bernoulli statistics.