Fenton-RAFT Polymerization: An "On-Demand" Chain-Growth Method

被引:46
|
作者
Reyhani, Amin [1 ]
McKenzie, Thomas G. [1 ]
Ranji-Burachaloo, Hadi [1 ]
Fu, Qiang [1 ]
Qiao, Greg G. [1 ]
机构
[1] Univ Melbourne, Dept Chem & Biomol Engn, Polymer Sci Grp, Parkville, Vic 3010, Australia
基金
澳大利亚研究理事会;
关键词
fenton; hydroxyl radicals; programmable polymer synthesis; adical polymerization; RAFT; LIVING RADICAL POLYMERIZATION; FUNCTIONAL POLYMERS; CHEMICAL-SYNTHESIS; HYDROGEN-PEROXIDE; OXYGEN TOLERANCE; AQUEOUS-SOLUTION; END; REAGENT; ACID; PHARMACEUTICALS;
D O I
10.1002/chem.201701410
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fine control over the architecture and/or microstructure of synthetic polymers is fast becoming a reality owing to the development of efficient and versatile polymerization techniques and conjugation reactions. However, the transition of these syntheses to automated, programmable, and high-throughput operating systems is a challenging step needed to translate the vast potential of precision polymers into machine-programmable polymers for biological and functional applications. Chain-growth polymerizations are particularly appealing for their ability to form structurally and chemically well-defined macromolecules through living/controlled polymerization techniques. Even using the latest polymerization technologies, the macromolecular engineering of complex functional materials often requires multi-step syntheses and purification of intermediates, and results in sub-optimal yields. To develop a proof-of-concept of a framework polymerization technique that is readily amenable to automation requires several key characteristics. In this study, a new approach is described that is believed to meet these requirements, thus opening avenues toward automated polymer synthesis.
引用
收藏
页码:7221 / 7226
页数:6
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