Grignard-based anionic ring-opening polymerization of propylene oxide activated by triisobutylaluminum

被引:13
|
作者
Roos, Kevin
Carlotti, Stephane [1 ]
机构
[1] Univ Bordeaux, Lab Chim Polymeres Organ, ENSCBP, F-33607 Pessac, France
关键词
Grignard reagent; Deprotonation; Monomer activation; Anionic ring-opening polymerization; Poly(propylene oxide); Polyethers; Magnesium counterion; ETHYLENE-OXIDE; CROWN-ETHER; DIMETHYL-SULFOXIDE; EPOXIDES; POLYETHER; COPOLYMERIZATION; BROMIDE; POLYOLS; CESIUM; SALTS;
D O I
10.1016/j.eurpolymj.2015.07.016
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Better known as alkylating agents, Grignard reagents are investigated as deprotonating agents of an alcohol to generate magnesium alkoxides for the initiation and propagation of the anionic ring-opening polymerization of propylene oxide. By using an excess of triisobutylaluminum, this magnesium-aluminum system enables a full conversion polymerization in a few hours yielding controlled poly(propylene oxide) up to 10000 g/mol with relatively low dispersity. Characterizations by NMR and MALDI-ToF-mass spectrometry allowed the determination of the chain-ends and therefore the associated initiation mechanisms. This study revealed that propylene oxide can be polymerized in presence of a magnesium-based counter-ion. Concomitant initiations by alkoxide, halide and hydride are discussed. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:240 / 246
页数:7
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