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m-吡啶-脲低聚物的尺寸控制自组装及其仿生物氯离子通道。

Self-Assembly of Size-Controlled m-Pyridine-Urea Oligomers and Their Biomimetic Chloride Ion Channels.

机构信息

Beijing Institute of Brain Disorders, Laboratory of Brain Disorders, Ministry of Science and Technology, Collaborative Innovation Center for Brain Disorders, Beijing Advanced Innovation Center for Big Data-based Precision Medicine, Capital Medical University, Beijing, 100069, China.

School of Pharmaceutical Science, Capital Medical University, Beijing, 100069, China.

出版信息

Angew Chem Int Ed Engl. 2021 May 3;60(19):10833-10841. doi: 10.1002/anie.202102174. Epub 2021 Apr 6.

Abstract

The m-pyridine urea (mPU) oligomer was constructed by using the intramolecular hydrogen bond formed by the pyridine nitrogen atom and the NH of urea and the intermolecular hydrogen bond of the terminal carbonyl group and the NH of urea. Due to the synergistic effect of hydrogen bonds, mPU oligomer folds and exhibits strong self-assembly behaviour. Affected by folding, mPU oligomer generates a twisted plane, and one of its important features is that the carbonyl group of the urea group orientates outwards from the twisted plane, while the NHs tend to direct inward. This feature is beneficial to NH attraction for electron-rich species. Among them, the trimer self-assembles into helical nanotubes, and can efficiently transport chloride ions. This study provides a novel and efficient strategy for constructing self-assembled biomimetic materials for electron-rich species transmission.

摘要

m-吡啶基脲(mPU)低聚物是通过吡啶氮原子与脲的 NH 之间形成的分子内氢键和末端羰基与脲的 NH 之间形成的分子间氢键构建的。由于氢键的协同作用,mPU 低聚物折叠并表现出强烈的自组装行为。受折叠影响,mPU 低聚物产生扭曲平面,其重要特征之一是脲基的羰基从扭曲平面向外定向,而 NHs 则倾向于向内定向。这一特征有利于 NH 对富电子物质的吸引力。其中,三聚体自组装成螺旋纳米管,可有效传输氯离子。本研究为构建富电子物质传输的仿生自组装材料提供了一种新颖有效的策略。

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