Aluminum Schiff Base Catalyst for Ring-opening Polymerization of ε-Caprolactone

被引:2
|
作者
Qu Zhi [1 ,2 ]
Li Xiang [1 ]
Pang Xuan [1 ]
Duan Ranlong [1 ]
Gao Bo [1 ]
Chen Xuesi [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
epsilon-Caprolactone; Ring-opening polymerization; Schiff base aluminun catalyst; CYCLIC ESTERS; STEREOSELECTIVE POLYMERIZATION; PROPYLENE-OXIDE; COMPLEXES; LACTIDES; LIGANDS; SPECTROSCOPY; MECHANISM; COPOLYMER; SINGLE;
D O I
10.7503/cjcu20130959
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The catalysts with high activity and low toxicity for ring opening polymerization(ROP) of epsilon-caprolactone had drawn much attention both in academia and industry. A series of asymmetric Schiff base aluminum complexes containing ligands that differed in their steric properties were synthesized. Their catalytic properties in the solution polymerization of epsilon-CL were examined. The kinetics studies of all complexes/2-propanol indicated that all of polymerizations were first-ordered reaction to monomers, and the polymerization rate of electrophilic substituted complex was about 4 times the non-electrophilic substituted complex in ROP of epsilon-CL. The results evaluated that the electrophilic substituent of ligands ha great influence on the catalytic activity of the complex.
引用
收藏
页码:869 / 872
页数:4
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