Sequence-defined multifunctional polyethers via liquid-phase synthesis with molecular sieving (vol 11, pg 136, 2018)

被引:4
|
作者
Dong, Ruijiao
Liu, Ruiyi
Gaffney, Piers R. J.
Schaepertoens, Marc
Marchetti, Patrizia
Williams, Christopher M.
Chen, Rongjun
Livingston, Andrew G.
机构
[1] Department of Chemical Engineering, Imperial College London, London
[2] EPSRC UK National Mass Spectrometry Facility (NMSF), Swansea University Medical School, Swansea
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1038/s41557-019-0212-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetic chemists have devoted tremendous effort towards the production of precision synthetic polymers with defined sequences and specific functions. However, the creation of a general technology that enables precise control over monomer sequence, with efficient isolation of the target polymers, is highly challenging. Here, we report a robust strategy for the production of sequence-defined synthetic polymers through a combination of liquid-phase synthesis and selective molecular sieving. The polymer is assembled in solution with real-time monitoring to ensure couplings proceed to completion, on a three-armed star-shaped macromolecule to maximize efficiency during the molecular sieving process. This approach is applied to the construction of sequence-defined polyethers, with side-arms at precisely defined locations that can undergo site-selective modification after polymerization. Using this versatile strategy, we have introduced structural and functional diversity into sequence-defined polyethers, unlocking their potential for real-life applications in nanotechnology, healthcare and information storage. © 2018, The Author(s), under exclusive licence to Springer Nature Limited.
引用
收藏
页码:184 / 184
页数:1
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