Abstract
It was found that radical polymerization occurs when the mixture of p-methoxystyrene and styrene in the presence of electron acceptors is photoexcited in basic solvents. Concomitantly, p-methoxystyrenestyrene co-dimers: trans-1-(4′-methoxyphenyl)-2-phenyl-cyclobutane and 1-(4′-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene are produced. From the results of some polymerization runs and the co-dimer structure, it is considered that the linear co-dimer cation radical is the common precursor for both radical polymerization and cationic dimerization, and the radical polymerization is initiated by its radical end.
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