Extremely rapid and versatile synthesis of high molecular weight step growth polymers via oxime click chemistry

被引:17
作者
Collins, Joe [1 ]
Xiao, Zeyun [1 ]
Espinosa-Gomez, Andrea [1 ]
Fors, Brett P. [2 ]
Connal, Luke A. [1 ]
机构
[1] Univ Melbourne, Dept Chem & Biomol Engn, Melbourne, Vic 3010, Australia
[2] Dept Chem & Chem Biol, Ithaca, NY 14853 USA
关键词
CROSS-LINKING; HYDROGELS; PH; POLYMERIZATION; LIGATION; DENDRIMERS; EFFICIENT; DELIVERY; LINKAGE; ROBUST;
D O I
10.1039/c6py00372a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Extremely rapid step growth polymerization was achieved using an oxime click chemistry approach. The highly efficient oxime reaction resulted in the synthesis of 35 kDa polymers within 5 minutes at 60 degrees C and 32 kDa polymers within 13 minutes at room temperature and, by altering the monomer ratio, polymers were synthesized with controlled end-group chemistry. Furthermore, the versatility of this chemistry was demonstrated by polymerisation of functional (bipyridine and boronic acid functional) monomers. The very rapid formation, extremely benign reaction conditions, functional group tolerance and high molecular weights obtained indicate the potential of oxime chemistry as a versatile tool for step-growth polymer synthesis.
引用
收藏
页码:2581 / 2588
页数:8
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