首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Supramolecular Chirality in Azobenzene-Containing Polymer System: Traditional Postpolymerization Self-Assembly Versus In Situ Supramolecular Self-Assembly Strategy
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Supramolecular Chirality in Azobenzene-Containing Polymer System: Traditional Postpolymerization Self-Assembly Versus In Situ Supramolecular Self-Assembly Strategy

机译:含偶氮苯的聚合物体系中的超分子手性:传统的晚期细聚合自组装与原位超分子自组装策略相比

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摘要

Recently, the design of novel supramolecular chiral materials has received a great deal of attention due to rapid developments in the fields of supramolecular chemistry and molecular self-assembly. Supramolecular chirality has been widely introduced to polymers containing photoresponsive azobenzene groups. On the one hand, supramolecular chiral structures of azobenzene-containing polymers (Azo-polymers) can be produced by nonsymmetric arrangement of Azo units through noncovalent interactions. On the other hand, the reversibility of the photoisomerization also allows for the control of the supramolecular organization of the Azo moieties within polymer structures. The construction of supramolecular chirality in Azo-polymeric self-assembled system is highly important for further developments in this field from both academic and practical points of view. The postpolymerization self-assembly strategy is one of the traditional strategies for mainly constructing supramolecular chirality in Azo-polymers. The in situ supramolecular self-assembly mediated by polymerization-induced self-assembly (PISA) is a facile one-pot approach for the construction of well-defined supramolecular chirality during polymerization process. In this review, we focus on a discussion of supramolecular chirality of Azo-polymer systems constructed by traditional postpolymerization self-assembly and PISA-mediated in situ supramolecular self-assembly. Furthermore, we will also summarize the basic concepts, seminal studies, recent trends, and perspectives in the constructions and applications of supramolecular chirality based on Azo-polymers with the hope to advance the development of supramolecular chirality in chemistry.
机译:最近,由于超分子化学和分子自组装的田地的快速发展,新型超分子手性材料的设计得到了大量的关注。已经广泛地将超分子手性被广泛引入含有光散偶氮苯基的聚合物。一方面,含三十苯的聚合物(偶氮聚合物)的超分子手性结构可以通过非共价相互作用的偶氮单元的非对称布置来制备。另一方面,光硅白化的可逆性还允许控制聚合物结构中的偶氮部分的超分子组织。偶氮聚合物自组装系统中超分子手性的构建对于本领域的进一步发展,从学术和实践的观点中的进一步发展非常重要。产后自组装策略是主要在偶氮聚合物中构建超分子手术的传统策略之一。由聚合诱导的自组装(PISA)介导的原位超分子自组装是在聚合过程中构建良好定义的超分子手术的容易的单罐方法。在本文中,我们专注于讨论由传统的晚期后分子自组装和PISA介导的偶氮聚合物体系的超分子手术讨论原位超分子自组装。此外,我们还将总结基于偶氮聚合物的超分子手性的基本概念,开创性研究,最近的趋势和观点,并希望在化学中提高超分子手术的发展。

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