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通过刺激诱导的聚合物结构转变实现的高分子形态变化。

Macromolecular metamorphosis via stimulus-induced transformations of polymer architecture.

机构信息

George &Josephine Butler Polymer Research Laboratory, Center for Macromolecular Science &Engineering, Department of Chemistry, University of Florida, PO Box 117200, Gainesville, USA.

出版信息

Nat Chem. 2017 Aug;9(8):817-823. doi: 10.1038/nchem.2730. Epub 2017 Feb 20.

Abstract

Macromolecular architecture plays a pivotal role in determining the properties of polymers. When designing polymers for specific applications, it is not only the size of a macromolecule that must be considered, but also its shape. In most cases, the topology of a polymer is a static feature that is inalterable once synthesized. Using reversible-covalent chemistry to prompt the disconnection of chemical bonds and the formation of new linkages in situ, we report polymers that undergo dramatic topological transformations via a process we term macromolecular metamorphosis. Utilizing this technique, a linear amphiphilic block copolymer or hyperbranched polymer undergoes 'metamorphosis' into comb, star and hydrophobic block copolymer architectures. This approach was extended to include a macroscopic gel which transitioned from a densely and covalently crosslinked network to one with larger distances between the covalent crosslinks when heated. These architectural transformations present an entirely new approach to 'smart' materials.

摘要

高分子结构在决定聚合物性质方面起着关键作用。在为特定应用设计聚合物时,不仅要考虑大分子的大小,还要考虑其形状。在大多数情况下,聚合物的拓扑结构是合成后不可改变的静态特征。通过可逆共价化学促使化学键的断开和新键的原位形成,我们报告了通过我们称之为高分子变形的过程经历剧烈拓扑转变的聚合物。利用该技术,线性两亲嵌段共聚物或超支化聚合物经历“变形”,形成梳状、星形和疏水嵌段共聚物结构。该方法扩展到包括宏观凝胶,当加热时,该凝胶从密集且共价交联的网络转变为共价交联之间具有更大距离的网络。这些结构转变为“智能”材料提供了一种全新的方法。

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