Cationic polymerization of 3-ethyl-3-hydroxymethyloxetane in an ionic liquid

被引:29
作者
Biedron, T [1 ]
Bednarek, M [1 ]
Kubisa, P [1 ]
机构
[1] Polish Acad Sci, Ctr Mol & Macromol Studies, PL-90363 Lodz, Poland
关键词
branched polyethers; cationic polymerization; ionic liquid;
D O I
10.1002/marc.200300294
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cationic ring-opening polymerization of 3-ethyl-3-hydroxymethyloxetane (EOX) in a neutral ionic liquid (1-butyl-3-methylimidazolium tetrafluoroborate, [bmim][BF4]) leading to a multihydroxyl, branched polyether proceeds readily to nearly quantitative conversion. Because of the relatively high polarity of ionic liquids, intermolecular hydrogen bonding leading to the formation of aggregates is reduced considerably. On the other hand, intramolecular hydrogen bonding facilitating intramolecular chain transfer is not significantly affected and the molecular weights of polymers are in the same range as those obtained in bulk polymerization or polymerization in organic solvents.
引用
收藏
页码:878 / 881
页数:4
相关论文
共 40 条
[1]  
Abdul-Sada AK, 1995, World Pat., Patent No. [WO 95 21872, 9521872]
[2]  
ABDULSADA AK, 1995, Patent No. 9521871
[3]  
[Anonymous], 2003, IONIC LIQUIDS SYNTHE
[4]  
[Anonymous], [No title captured], Patent No. 0032658
[5]  
ATKINS MP, 1997, Patent No. 0791643
[6]   Multihydroxyl branched polyethers. 2. Mechanistic aspects of cationic polymerization of 3-ethyl-3-(hydroxymethyl)oxetane [J].
Bednarek, M ;
Kubisa, P ;
Penczek, S .
MACROMOLECULES, 2001, 34 (15) :5112-5119
[7]   Chain-growth limiting reactions in the cationic polymerization of 3-ethyl-3-hydroxymethyloxetane [J].
Bednarek, M ;
Kubisa, P .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2004, 42 (02) :245-252
[8]   Multihydroxyl branched polyethers by cationic copolymerization of hydroxymethyl oxetanes: copolymerization of 3-ethyl-3-(hydroxymethyl) oxetane with difunctional oxetane [J].
Bednarek, M .
POLYMER INTERNATIONAL, 2003, 52 (10) :1595-1599
[9]  
Bednarek M, 1999, MACROMOL RAPID COMM, V20, P369, DOI 10.1002/(SICI)1521-3927(19990701)20:7<369::AID-MARC369>3.0.CO
[10]  
2-S