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由变构金属模板调控的可逆氢键聚合。

Reversible hydrogen-bonded polymerization regulated by allosteric metal templation.

机构信息

Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, 213164, China.

出版信息

Chem Commun (Camb). 2020 Nov 19;56(92):14385-14388. doi: 10.1039/d0cc06381a.

DOI:10.1039/d0cc06381a
PMID:33140747
Abstract

Allosteric effects are common in biology, but have not been fully explored in the control of supramolecular polymerization. Herein, ditopic UPy derivatives with acyclic crown ether-like spacers were designed and synthesized, which can undergo supramolecular polymerization through quadruple hydrogen bonding. Upon the addition of K+, drastic molecular conformational change to the U-shape is induced by metal-coordination, reconfiguring remote UPy sites towards the formation of discrete cyclic dimers. Interestingly, the supramolecular polymerization can be restored by simply removing K+ by water-extraction.

摘要

变构效应在生物学中很常见,但在超分子聚合的控制中尚未得到充分探索。在此,设计并合成了具有非循环冠醚状间隔基的双位点 UPy 衍生物,它们可以通过四重氢键进行超分子聚合。加入 K+后,金属配位诱导分子构象发生剧烈的 U 型变化,远程 UPy 位点重新配置形成离散的环状二聚体。有趣的是,通过简单的水萃取去除 K+即可恢复超分子聚合。

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