The synthesis of 2,4-dihydroxy-4’-vinylbenzophenone was accomplished in five steps, with an overall yield of 15%, starting with p-ethylbenzoic acid. Pure 2,4-dihydroxy-4’-vinylbenzophenone was polymerized with azobis(isobutyr0)nitrile initiator; radical copolymerizations with methacrylic acid and styrene were also accomplished. In polymerizations with azobis(isobutyro)nitrile, no interference of the phenol groups of 2,4-dihydroxy-4’-vinylbenzophenone was observed. In copolymerization with styrene using benzoyl peroxide as initiator, the molecular weight of a copolymer containing 3 mol % 2,4-dihydroxy-4’-vinylbenzophenone was found to be significantly higher that of styrene homopolymer prepared under identical conditions. This effect was also observed in the polymerization styrene in the presence of a model compound, 2,4-dihydroxy-4’-ethylbenzophenone.
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Bailey et al. (1978) studied this question.
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