Polyether synthesis: From activated or metal-free anionic ring-opening polymerization of epoxides to functionalization

被引:238
作者
Brocas, Anne-Laure [1 ]
Mantzaridis, Christos [1 ]
Tunc, Deniz [1 ]
Carlotti, Stephane [1 ]
机构
[1] Univ Bordeaux, CNRS, LCPO, UMR 5629, F-33600 Pessac, France
关键词
Polyether; Anionic polymerization; Controlled/living polymerization; Ring-opening polymerization; Activation; Functionalized polymers; Epoxides; HIGH-MOLECULAR-WEIGHT; SELF-ASSEMBLED MONOLAYERS; N-HETEROCYCLIC CARBENES; HETEROBIFUNCTIONAL POLY(ETHYLENE GLYCOL); ROOM-TEMPERATURE POLYMERIZATION; 9-METHYLFLUORENYL ALKALI SALTS; PROPYLENE-OXIDE POLYMERIZATION; STAR-SHAPED POLYGLYCIDOLS; PHOSPHAZENE BASE T-BUP4; GLYCIDYL PHENYL ETHER;
D O I
10.1016/j.progpolymsci.2012.09.007
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Epoxide derivatives constitute a broad family of monomers which are able to be polymerized by anionic or related nucleophilic ring-opening mechanism. The main synthetic strategies developed are reviewed in terms of polymerization rates, side reactions, and possibilities for controlling such polymerizations. Ring-opening polymerization of ethylene oxide and substituted epoxides utilizing alkali metal derivatives or other initiating systems in conjunction or not with activating systems are discussed. Emphasis is also given on the use of organic initiators or catalysts to trigger the metal-free ring-opening polymerization of epoxides. Functionalization of polyethers is also described, which includes the use of functional initiators, post-chemical modification of reactive functions carried by the polyether backbone, or functional-monomer insertion. A focus is particularly given on the preparation of polyethers bearing hydroxy, amine, allyl, azide and other reactive groups, at the chain ends or in the chains. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:845 / 873
页数:29
相关论文
共 248 条
[1]  
AIDA T, 1981, MAKROMOL CHEM, V182, P1073
[2]   LIVING POLYMERIZATION OF EPOXIDES WITH METALLOPORPHYRIN AND SYNTHESIS OF BLOCK COPOLYMERS WITH CONTROLLED CHAIN LENGTHS [J].
AIDA, T ;
INOUE, S .
MACROMOLECULES, 1981, 14 (05) :1162-1166
[3]   Metalloporphyrins as initiators for living and immortal polymerizations [J].
Aida, T ;
Inoue, S .
ACCOUNTS OF CHEMICAL RESEARCH, 1996, 29 (01) :39-48
[4]   COPOLYMERIZATION OF EPOXIDES BY ALUMINUM PORPHYRIN - REACTIVITY OF (PORPHINATO)ALUMINUM ALKOXIDE AS GROWING SPECIES [J].
AIDA, T ;
WADA, K ;
INOUE, S .
MACROMOLECULES, 1987, 20 (02) :237-241
[5]   HIGH-SPEED IMMORTAL POLYMERIZATION OF EPOXIDES INITIATED WITH ALUMINUM PORPHYRIN - ACCELERATION OF PROPAGATION AND CHAIN-TRANSFER REACTIONS BY A LEWIS-ACID [J].
AKATSUKA, M ;
AIDA, T ;
INOUE, S .
MACROMOLECULES, 1994, 27 (10) :2820-2825
[6]   Synthesis of heterotelechelic poly(ethylene glycol) derivatives having α-benzaldehyde and ω-pyridyl disulfide groups by ring opening polymerization of ethylene oxide using 4-(diethoxymethyl)benzyl alkoxide as a novel initiator [J].
Akiyama, Y ;
Nagasaki, Y ;
Kataoka, K .
BIOCONJUGATE CHEMISTRY, 2004, 15 (02) :424-427
[7]   Synthesis of hydrophobic poly(alkylene oxide)s and amphiphilic poly(alkylene oxide) block copolymers [J].
Allgaier, Juergen ;
Willbold, Sabine ;
Chang, Taihyun .
MACROMOLECULES, 2007, 40 (03) :518-525
[8]  
[Anonymous], ACS SYM SER
[9]  
[Anonymous], POLYM SCI USSR
[10]  
[Anonymous], 1972, POLYM SCI USSR