Rapid and quantitative one-pot synthesis of sequence-controlled polymers by radical polymerization

被引:390
作者
Gody, Guillaume [1 ,2 ]
Maschmeyer, Thomas [2 ]
Zetterlund, Per B. [3 ]
Perrier, Sebastien [1 ]
机构
[1] Univ Sydney, Sch Chem, Key Ctr Polymers & Colloids, Sydney, NSW 2006, Australia
[2] Univ Sydney, Sch Chem, Lab Adv Catalysis Sustainabil, Sydney, NSW 2006, Australia
[3] Univ New S Wales, Sch Chem Engn, CAMD, Sydney, NSW 2052, Australia
来源
NATURE COMMUNICATIONS | 2013年 / 4卷
基金
澳大利亚研究理事会;
关键词
FRAGMENTATION CHAIN TRANSFER; MULTIBLOCK COPOLYMERS; PEPTIDE-SYNTHESIS; RAFT PROCESS; DESIGN; ACIDS;
D O I
10.1038/ncomms3505
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A long-standing challenge in polymer chemistry has been to prepare synthetic polymers with not only well-defined molecular weight, but also precisely controlled microstructure in terms of the distribution of monomeric units along the chain. Here we describe a simple and scalable method that enables the synthesis of sequence-controlled multiblock copolymers with precisely defined high-order structures, covering a wide range of functional groups. We develop a one-pot, multistep sequential polymerization process with yields >99%, giving access to a wide range of such multifunctional multiblock copolymers. To illustrate the enormous potential of this approach, we describe the synthesis of a dodecablock copolymer, a functional hexablock copolymer and an icosablock (20 blocks) copolymer, which represents the largest number of blocks seen to date, all of very narrow molecular weight distribution for such complex structures. We believe this approach paves the way to the design and synthesis of a new generation of synthetic polymers.
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页数:9
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