Synthesis of N-acryloxysuccinimide copolymers by RAFT polymerization, as reactive building blocks with full control of composition and molecular weights

被引:89
作者
Favier, A [1 ]
D'Agosto, F [1 ]
Charreyre, MT [1 ]
Pichot, C [1 ]
机构
[1] Ecole Normale Super Lyon, CNRS, Unite Mixte BioMeriuex, F-69364 Lyon 07, France
关键词
RAFT copolymerization; watersoluble reactive copolymers; activated ester derivative;
D O I
10.1016/j.polymer.2004.09.042
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The reversible addition-fragmentation chain transfer (RAFT) polymerization process was used to synthesize well-defined N-acryloxysuccinimide (NAS) based copolymers, very useful reactive building blocks for various applications. Kinetic studies of RAFT copolymerization of NAS with a bi-substituted acrylamide derivative, N-acryloylmorpholine (NAM), were performed in the presence of tertbutyl dithiobenzoate (tBDB). An excellent control was reached with very high conversions (>95%), molecular weights (MW) up to 80 000 g mol(-1) and very narrow molecular weight distributions (MWD) (polydispersity indices, PDI < 1.1), as determined by aqueous size exclusion chromatography with on-line light scattering detector (SEC/LS). In addition, the comparison of RAFT and conventional NAM/NAS free radical copolymerization indicated that the apparent reactivity ratios in RAFT are similar to the reactivity ratios determined from conventional copolymerization. An identical azeotropic composition (60/40 NAM/NAS molar ratio) was obtained providing perfectly random poly(NAM-co-NAS) copolymers with full control of composition and MW. These copolymer chains with regularly-distributed reactive functions can be integrated into more complex architectures. As an example, poly [(NAM-co-NAS)-b-NAM] block copolymers with length-varying poly(NAM) block were synthesized with a very efficient control over MW, MWD and composition. (C) 2004 Published by Elsevier Ltd.
引用
收藏
页码:7821 / 7830
页数:10
相关论文
共 89 条
[1]   DETERMINATION OF THE REACTIVITY RATIOS, SEQUENCE DISTRIBUTION AND STEREOREGULARITY OF BUTYL ACRYLATE-METHYL METHACRYLATE COPOLYMERS BY MEANS OF PROTON AND C-13 NMR [J].
AERDTS, AM ;
GERMAN, AL ;
VANDERVELDEN, GPM .
MAGNETIC RESONANCE IN CHEMISTRY, 1994, 32 :S80-S88
[2]  
AREHART SV, 1999, POLYM PREPR AM CHEM, V40, P458
[3]  
ARSHADY R, 1994, ADV POLYM SCI, V111, P1
[4]   Quenching studies of hydrophobically-modified poly(N-isopropylacrylamides) [J].
Barros, TC ;
Adronov, A ;
Winnik, FM ;
Bohne, C .
LANGMUIR, 1997, 13 (23) :6089-6094
[5]   MODEL REACTIONS FOR SYNTHESIS OF PHARMACOLOGICALLY ACTIVE POLYMERS BY WAY OF MONOMERIC AND POLYMERIC REACTIVE ESTERS [J].
BATZ, HG ;
FRANZMANN, G ;
RINGSDORF, H .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1972, 11 (12) :1103-1104
[6]   Synthesis of polymer brushes on silicate substrates via reversible addition fragmentation chain transfer technique [J].
Baum, M ;
Brittain, WJ .
MACROMOLECULES, 2002, 35 (03) :610-615
[7]   Development of a universal alkoxyamine for "living" free radical polymerizations [J].
Benoit, D ;
Chaplinski, V ;
Braslau, R ;
Hawker, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (16) :3904-3920
[8]   RADICAL POLYMERIZATION OF 2-AMINOMETHYLMETHACRYLATES WITH METHYLMETHACRYLATE [J].
CAMAIL, M ;
ESSAOUDI, H ;
MARGAILLAN, A ;
VERNET, JL .
EUROPEAN POLYMER JOURNAL, 1995, 31 (11) :1119-1125
[9]   Dependence of chemical composition of styrene/butyl acrylate copolymers on temperature and molecular weight [J].
Chambard, G ;
Klumperman, B ;
German, AL .
POLYMER, 1999, 40 (16) :4459-4463
[10]  
Chambard G., 2000, ACS SYM SER, V768, P197