SYNTHESIS AND REACTIONS OF TELECHELIC POLYACETALS

被引:23
作者
GOETHALS, EJ
DECLERCQ, RR
DECLERCQ, HC
HARTMANN, PJ
机构
[1] Laboratory of Organic Chem., Polymer Chemistry Division, University of Ghent, Ghent, B-9000
来源
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA | 1991年 / 47卷
关键词
D O I
10.1002/masy.19910470113
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Telechelic polyacetals have been synthesized by endcapping of bifunctionally living polyacetals with tertiary amines. Bifunctionally living poly-(1,3-dioxolane) (poly-DXL) was obtained by polymerization of the cyclic acetal initiated with terephthaloyl-bis-triflate. Attempts to prepare well defined bifunctionally growing poly-DXL with trifluoro-methane sulfonic acid anhydride failed. Low molecular weight dialkyl formals containing functional groups were used as transfer agents for the polymerization of cyclic acetals to control the molecular weight of the polymer and to introduce functional endgroups. Polytelechelic hydroxy-terminated poly-DXL was synthesized by copolymerization of DXL and glycidol. The latter monomer reacts as comonomer through its epoxy ring and as transfer agent by its hydroxyl group.
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页码:151 / 162
页数:12
相关论文
共 10 条
[1]   POLYMERIZATION AND COPOLYMERIZATION OF TRIOXANE - FACTORS INFLUENCING MOLECULAR-WEIGHT AND END GROUPS [J].
CHEN, CSH .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1975, 13 (05) :1183-1208
[2]  
CHIALKOWSKA W, 1982, MAKROMOL CHEM, V183, P753
[3]   CHAIN EXTENSION OF OLIGODIOLS BY MEANS OF CYCLIC ACETALS [J].
FRANTA, E ;
KUBISA, P ;
REFAI, J ;
KADA, SO ;
REIBEL, L .
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA, 1988, 13-4 :127-144
[4]  
HERMANN HD, 1966, MAKROMOLEKUL CHEM, V90, P1
[5]  
MASAMOTO J, 1990, ACS POLYM PREPRINTS, V31, P82
[6]  
PENCZEK S, 1973, MAKROMOL CHEM, V172, P243
[7]  
PENCZEK S, 1974, MAKROMOL CHEM, V175, P1217
[8]  
PENCZEK S, 1989, COMPREHENSIVE POLYM, V3, P787
[9]  
SCHULZ RC, 1984, RING OPENING POLYM, V1, P369
[10]  
VANMEIRVENNE D, 1989, MAKROMOL CHEM S, V15, P61