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Synthesis of hyperbranched polymers via a facile self-condensing vinyl polymerization system - Glycidyl methacrylate/Cp2TiCl2/Zn
被引:14
|作者:
Liu, Xiao-hui
[1
]
Bao, You-mei
[1
]
Tang, Xiu-lan
[2
]
Li, Yue-sheng
[1
,2
]
机构:
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Yanshan Univ, Coll Environm & Chem Engn, Qinhuangdao 066004, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Hyperbranched;
Self-condensing vinyl polymerization (SCVP);
Poly(epsilon-caprolactone);
ONE-POT SYNTHESIS;
RING-OPENING POLYMERIZATION;
RADICAL STYRENE POLYMERIZATIONS;
BLOCK-COPOLYMERS;
EPSILON-CAPROLACTONE;
BRANCHED POLY(N-ISOPROPYLACRYLAMIDE);
L-LACTIDE;
EPOXIDE;
ATRP;
POLYSTYRENE;
D O I:
10.1016/j.polymer.2010.04.034
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
A facile self-condensing vinyl polymerization (SCVP) system, the combination of glycidyl methacrylate, Cp2TiCl2 and Zn, has been firstly used to prepare novel hyperbranched polymers, consisting of vinyl polymers as the backbone, and cyclic ester polymers (poly(c-caprolactone) or poly(L-lactide)) as the side chains. The polymerizations are initiated by the epoxide radical ring-opening catalyzed by Cp2Ti(III)Cl which is generated in situ via the reaction of Cp2TiCl2 with Zn. The key to success is that the polymerizations can proceed concurrently via two dissimilar chemistries possessing the opposite active initiating species, including ring-opening polymerization (ROP) and controlled/living radical polymerization (CRP). We have demonstrated that this facile one-step polymerization technique can be applied successfully to prepare highly branched polymers with a multiplicity of end reactive functionalities including Ti alkoxide, hydroxyl and vinyl functional groups. (C) 2010 Elsevier Ltd. All rights reserved.
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页码:2857 / 2863
页数:7
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