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Tailored polymer microstructures prepared by atom transfer radical copolymerization of styrene and N-substituted maleimides

机译:通过苯乙烯和N-取代的马来酰亚胺的原子转移自由基共聚制备的定制聚合物微结构

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摘要

In the present Feature Article, a kinetic strategy for controlling the microstructure of synthetic polymer chains prepared via a radical chain-growth polymerization process is presented. This approach was recently developed in our laboratory and relies on the controlled kinetic addition of ultrareactive N-substituted maleimides during the atom transfer radical polymerization of styrene. This method is experimentally straightforward and can be applied to a broad library of functional N-substituted maleimides. Thus, this platform allows synthesis of unprecedented polymer materials such as 1D macromolecular arrays. The basic kinetic requirements, the experimental conditions, and the synthetic scope of this approach are discussed in details herein. The controlled radical copolymerization of styrene with N-substituted maleimides allows preparation of unique polymer microstructures. Indeed, we reported in recent years that small amounts of N-substituted maleimides can be placed at specific locations in linear polystyrene chains. Herein, we describe in details this research advance. The kinetic concept, the experimental conditions and the scope of this novel strategy are discussed in this feature article.
机译:在本专题文章中,提出了一种动力学策略,用于控制通过自由基链增长聚合工艺制备的合成聚合物链的微观结构。该方法是最近在我们实验室中开发的,它依赖于苯乙烯原子转移自由基聚合过程中超反应性N-取代的马来酰亚胺的受控动力学加成。该方法在实验上是简单明了的,可应用于功能性N取代马来酰亚胺的广泛文库。因此,该平台允许合成前所未有的聚合物材料,例如一维大分子阵列。本文详细讨论了该方法的基本动力学要求,实验条件和合成范围。苯乙烯与N-取代的马来酰亚胺的受控自由基共聚可以制备独特的聚合物微结构。确实,近年来我们报道了少量的N-取代的马来酰亚胺可以被放置在线性聚苯乙烯链的特定位置。在此,我们详细描述了这项研究进展。在这篇专题文章中讨论了这种新颖策略的动力学概念,实验条件和范围。

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