CO2-responsive polymeric materials: synthesis, self-assembly, and functional applications

被引:344
作者
Darabi, Ali [1 ,3 ]
Jessop, Philip G. [2 ]
Cunningham, Michael F. [1 ,2 ]
机构
[1] Queens Univ, Dept Chem Engn, Kingston, ON, Canada
[2] Queens Univ, Dept Chem, Kingston, ON, Canada
[3] Arkema Res & Dev Ctr, Funct Addit, King Of Prussia, PA USA
基金
加拿大自然科学与工程研究理事会;
关键词
CONTROLLED/LIVING RADICAL POLYMERIZATION; CARBON-DIOXIDE CAPTURE; SWITCHABLE HYDROPHILICITY SOLVENTS; FRAGMENTATION CHAIN TRANSFER; REVERSIBLE FIXATION-RELEASE; PH-RESPONSIVE POLYMERS; ONE-POT SYNTHESIS; BLOCK-COPOLYMER; EMULSION POLYMERIZATION; IONIC LIQUIDS;
D O I
10.1039/c5cs00873e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO2 is an ideal trigger for switchable or stimuli-responsive materials because it is benign, inexpensive, green, abundant, and does not accumulate in the system. Many different CO2-responsive materials including polymers, latexes, solvents, solutes, gels, surfactants, and catalysts have been prepared. This review focuses on the preparation, self-assembly, and functional applications of CO2-responsive polymers. Detailed discussion is provided on the synthesis of CO2-responsive polymers, in particular using reversible deactivation radical polymerization (RDRP), formerly known as controlled/living radical polymerization (CLRP), a powerful technique for the preparation of well-defined (co)polymers with precise control over molecular weight distribution, chain-end functional groups, and polymer architectural design. Self-assembly in aqueous dispersed media is highlighted as well as emerging potential applications.
引用
收藏
页码:4391 / 4436
页数:46
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