Stimuli-responsive hydrogels prepared by simultaneous "click chemistry" and metal-ligand coordination

被引:16
|
作者
Li, Yang [1 ]
Zhou, Chao [1 ]
Xu, Liqun [2 ]
Yao, Fang [1 ]
Cen, Lian [3 ,4 ]
Fu, Guo Dong [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Jiangsu, Peoples R China
[2] Southwest Univ, Inst Clean Energy & Adv Mat, Chongqing 400715, Peoples R China
[3] E China Univ Sci & Technol, Sch Chem Engn, Shanghai 200237, Peoples R China
[4] Natl Tissue Engn Ctr China, Shanghai 200241, Peoples R China
基金
中国国家自然科学基金;
关键词
SUPRAMOLECULAR RECOGNITION; GELS; POLYMERS; ORGANOGELS; COMPLEXES; GELATION; NETWORKS; POLYMERIZATION; CYCLOADDITION; DERIVATIVES;
D O I
10.1039/c4ra11946k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel strategy to synthesize stimuli-responsive metal-coordinated polymeric gels (MCPGs) via one-pot CuAAC and non-covalent metal coordination chemistry was demonstrated. 4'-(4-Prop-2-ynyloxyphenyl)-2,2 ':6 ',2 ''-terpyridine (Terpy-phi-CH2C equivalent to CH) and alpha,omega-diazido/hydroxyl PEG (PEG(45)(N-3)(2)) were used as precursors to yield linear terpyridine-terminated PEG derivatives with 1,2,3-triazole rings and terpyridine ligands in their main chains to serve as ligands for chelating a range of transition and/or lanthanide metal ions. It was found that the bridging metal complexes could not only act as branching or crosslinking sites within the three-dimensional polymer networks but could also bestow special properties to the final gels, such as stimuli-responsive and thixotropic features, thereby allowing facile and efficient design and synthesis of promising intelligent materials.
引用
收藏
页码:18242 / 18251
页数:10
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