摘要
以辛酸亚锡[Sn(Oct)2]为催化剂、乙二醇为引发剂,通过本体开环共聚,合成了己内酯(CAP)与三亚甲基碳酸酯(TMC)的共聚物。采用1H、13C核磁共振及同核二维相关谱(gCOSY)、13C-1H异核相关谱(gHSQC)和13C-1H异核远程相关谱(gHMBC)等二维核磁共振(2D NMR)技术,对所合成的聚合物进行了序列微结构表征,找出了聚合物分子链中序列连接方式,并完成了1H和13C NMR谱带的归属。
The copolymers of ε-caprolactone (CAP) and trimethylene carbonate ( TMC ) were synthesized by ring-opening bulk copolymerization using stannous octoate [ Sn(Oct) 2 ] as catalyst and ethylene glycol as initiator. The sequence microstructures of the resulting copolymers were characterized by ^1H, ^13C nuclear magnetic resonance spectroscopy ( ^1H and ^13C NMR) and two-dimensional nuclear magnetic resonance (2D NMR) techniques including homonuclear correlation spectroscopy with gradient(gCOSY) , ^1H detected heteronuclear single quantum coherence with gradient(gHSQC ) and ^1H detected heteronuclear multiple-bond coherence with gradient(gHMBC) etc. The linkage modes of sequence in the copolymer chain were found. The assignments of all ^1H and ^13C bands for the copolymers were completed.
出处
《分析化学》
SCIE
CAS
CSCD
北大核心
2008年第2期192-196,共5页
Chinese Journal of Analytical Chemistry
基金
辽宁省自然科学基金资助项目(No.20032149)
丹东市科技攻关项目(No.03111)
关键词
己内酯
聚己内酯
聚三亚甲基碳酸酯
序列结构
二维核磁共振波谱
ε-Caprolactone, poly(ε-caprolactone), poly(trimethylene carbonate), sequence structure, two- dimensional nuclear magnetic resonance spectrum