Cyclic Poly(ε-caprolactone) Synthesized by Combination of Ring-Opening Polymerization with Ring-Closing Metathesis, Ring Closing Enyne Metathesis, or "Click" Reaction

被引:32
|
作者
Xie, Meiran [1 ]
Shi, Jiaxin [1 ]
Ding, Liang [1 ]
Li, Jinxin [1 ]
Han, Huijing [1 ]
Zhang, Yiqun [1 ]
机构
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
基金
中国国家自然科学基金;
关键词
macrocycles; metathesis; poly(epsilon-caprolactone); ring-opening polymerization; GLYCOSIDES; COPOLYMER; POLYMERS; ROUTE; STAR; RCM;
D O I
10.1002/pola.23390
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This article described the synthesis of cyclic poly(epsilon-caprolactone) (PCL) via ring-closing metathesis (RCM), ring closing enyne metathesis (RCEM), and "click" reaction of difrerent difunctional linear PCL. Linear PCL precursors were prepared by ring-opening polymerization (ROP) of epsilon-caprolactone in bulk using 10-undecen-1-ol or propargyl alcohol as the initiator, followed by reacting with corresponding acyl chloride containing vinyl or azido end group. The subsequent end-to-end intramolecular coupling reactions were performed under high dilution conditions. The successful transformation of linear PCL precursor to cyclic PCL was confirmed by Gel permeation chromatography, H-1 NMR, and Fourier transform infrared measurements. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3022-3033, 2009
引用
收藏
页码:3022 / 3033
页数:12
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