期刊
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY
卷 A39, 期 9, 页码 991-1006出版社
MARCEL DEKKER INC
DOI: 10.1081/MA-120013575
关键词
diphenyl diselenide; beta-phenylethyl p-tert-butylphenyl selenide; 1,4-bis(p-tert-butylphenyl) diselenide; radical polymerization; photoiniferter; polymeric photoiniferter; block copolymer
Block copolymers of styrene and p-substituted styrene were prepared by photopolymerization of p-bromostyrene or p-methylstyrene in the presence of end functional polystyrene (DPDSE-PST) containing phenylseleno groups at the alpha and omega-chain ends as polymeric photoiniferter. To determine the form of resulting block copolymers, the behavior of chain terminals of DPDSE-PST was investigated. The ability of photoinitiate and chain transfer of P-phenylethyl p-tert-butylphertyl selenide as a model compound of alpha-chain end of DPDSE-PST was much smaller than that of benzyl phenyl selenide as a model compound of omega-chain end of DPDSE-PST. On the other hand, the polymerization of styrene, prepared by 1,4-Bis(p-tert-butylphenyl) diselenide as photoiniferter, with styrene also revealed a form of the resulting block copolymer was an AB block structure.
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