Dynamic covalent polymers: Reorganizable polymers with dynamic covalent bonds

被引:470
作者
Maeda, Takeshi [1 ]
Otsuka, Hideyuki [1 ]
Takahara, Atsushi [1 ]
机构
[1] Kyushu Univ, Inst Mat Chem & Engn, Nishi Ku, Fukuoka 8190395, Japan
关键词
Dynamic covalent chemistry; Reversible polymer; Dynamic covalent bond; Exchange reaction; Stimulus-responsive polymer; Dynamic combinatorial chemistry; RING-OPENING POLYMERIZATION; RADICAL CROSSOVER REACTION; INTERCHANGE REACTIONS; MECHANICAL-PROPERTIES; EQUILIBRIUM POLYMERIZATION; CONDENSATION COPOLYMERS; POLY(BISPHENOL-A CARBONATE); REVERSIBLE POLYMERIZATION; COMBINATORIAL CHEMISTRY; LINKING SYSTEM;
D O I
10.1016/j.progpolymsci.2009.03.001
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 recent research on dynamic covalent polymers is reviewed. These polymers exhibit dynamic features originating in the reversibility, of dynamic covalent bonds. The main body of the review is presented in four sections: (i) utilization of dynamic covalent bonds in reactive polymer blends, (ii) ring-chain equilibrium based on dynamic covalent bonds, (iii) reorganizable polymers and polymeric systems with dynamic covalent bonds, and (iv) dynamic smart polymer materials. Unlike conventional polymers that are irreversibly formed, dynamic covalent polymers can reform their structures and constitutions under appropriate conditions, even after polymerization. Utilization of dynamic covalent bonds is seen in research concerning polymerization controls and polymer blends. In addition, reorganizable macromolecules specially programmed to exhibit dynamic features have recently been highlighted in line with increased understanding of dynamic phenomena through reversible formation of non-covalent bonds. They include various dynamic covalent bonds typified by C=N bonds in imine derivatives and C-O bonds in alkoxyamine moieties, and are not only converted into macromolecules with different constitutions or gels, but also exhibit discriminating properties attributed to the reversibility, of dynamic covalent bonds by adequate external stimuli, such as heating and the addition of a catalyst. The trend of dynamic covalent polymers is directed to intelligent systems using equilibrium under reorganization processes and stimulus-responsive polymeric materials based on bond-reformation. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:581 / 604
页数:24
相关论文
共 132 条
[71]  
Kotliar A.M., 1981, J. Polym. Sci., V16, P367
[72]   Synthesis of macrocycles by the ring-crossover reaction of a cyclic dithioester [J].
Kudo, Hiroto ;
Makino, Shinya ;
Nishikubo, Tadatomi .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2007, 45 (04) :680-687
[73]   Dynamic combinatorial chemistry: on the road to fulfilling the promise [J].
Ladame, Sylvain .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2008, 6 (02) :219-226
[74]  
Lee S, 2001, J APPL POLYM SCI, V82, P1725, DOI 10.1002/app.2013
[75]   Dynamers: dynamic molecular and supramolecular polymers [J].
Lehn, JM .
PROGRESS IN POLYMER SCIENCE, 2005, 30 (8-9) :814-831
[76]  
Lehn JM, 1999, CHEM-EUR J, V5, P2455
[77]   Effect of Di-n-dodecyl phosphate on the transesterification reaction in a poly(butylene terephthalate)/polycarbonate blend [J].
Lei, Caihong ;
Chen, Dahua .
JOURNAL OF APPLIED POLYMER SCIENCE, 2008, 109 (02) :1099-1104
[78]   Dynamic mechanically interlocked dendrimers:: Amplification in dendritic dynamic combinatorial libraries [J].
Leung, Ken C. -F. ;
Arico, Fabio ;
Cantrill, Stuart J. ;
Stoddart, J. Fraser .
MACROMOLECULES, 2007, 40 (11) :3951-3959
[79]   Controlled release of volatile aldehydes and ketones by reversible hydrazone formation - "classical" profragrances are getting dynamic [J].
Levrand, Barbara ;
Ruff, Yves ;
Lehn, Jean-Marie ;
Herrmann, Andreas .
CHEMICAL COMMUNICATIONS, 2006, (28) :2965-2967
[80]   Thermodynamics of a diaminocarbene-tetraaminoethylene equilibrium [J].
Liu, YF ;
Lindner, PE ;
Lemal, DM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (45) :10626-10627