THE EFFECTS OF MONOMER STRUCTURE OF CYCLIC KETENE ACETALS ON THE BEHAVIOR OF CONTROLLED RADICAL RING-OPENING POLYMERIZATION*

Citation:   THE EFFECTS OF MONOMER STRUCTURE OF CYCLIC KETENE ACETALS ON THE BEHAVIOR OF CONTROLLED RADICAL RING-OPENING POLYMERIZATION*[J]. Chinese Journal of Polymer Science, 2002, 20(1): 9-14. shu

THE EFFECTS OF MONOMER STRUCTURE OF CYCLIC KETENE ACETALS ON THE BEHAVIOR OF CONTROLLED RADICAL RING-OPENING POLYMERIZATION*

摘要: Polymerization of three cyclic ketene acetals: i.e., 5,6-benzo-2-methylene-1,3-dioxepane (BMDO), 2-methylene-4-phenyl-1,3-dioxolane (MPDO) and 4, 7-dimethyl-2-methylene-1, 3-dioxepane(DMMDO) were carried out in the presence ofethyl α-bromobutyrate/CuBr/2, 2'-bipyridine respectively. The structures of poly(BMDO), poly(MPDO) and poly(DMMDO)were characterized by 1H and 13C-NMR spectra. The effects of monomer structure on the behavior of atom transfer freeradical ring-opening polymerization were investigated and the mechanism of controlled free radical ring-opening polymerization was discussed.

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  • 发布日期:  2002-02-20
  • 收稿日期:  2000-12-16
  • 修回日期:  2001-03-06
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

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