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多杂环分子链的可控折叠、动态和构象动态过程。

Controlled Folding, Motional, and Constitutional Dynamic Processes of Polyheterocyclic Molecular Strands.

机构信息

Institut Européen des Membranes, CNRS UMR 5635, Place Eugène Bataillon, CC 047, 34095, Montpellier, France.

Institut de Science et d'Ingénierie Supramoléculaires (UMR 7006), Université de Strasbourg, 8 Allée Gaspard Monge, 67000, Strasbourg, France.

出版信息

Angew Chem Int Ed Engl. 2016 Mar 18;55(13):4130-54. doi: 10.1002/anie.201505394. Epub 2016 Feb 19.

DOI:10.1002/anie.201505394
PMID:26894262
Abstract

General design principles have been developed for the control of the structural features of polyheterocyclic strands and their effector-modulated shape changes. Induced defined molecular motions permit designed enforcement of helical as well as linear molecular shapes. The ability of such molecular strands to bind metal cations allows the generation of coiling/uncoiling processes between helically folded and extended linear states. Large molecular motions are produced on coordination of metal ions, which may be made reversible by competition with an ancillary complexing agent and fueled by sequential acid/base neutralization energy. The introduction of hydrazone units into the strands confers upon them constitutional dynamics, whereby interconversion between different strand compositions is achieved through component exchange. These features have relevance for nanomechanical devices. We present a morphological and functional analysis of such systems developed in our laboratories.

摘要

已经制定出控制多杂环链状结构特征及其效应器调制形状变化的一般设计原则。诱导的特定分子运动允许对螺旋和线性分子形状进行有针对性的强化。这些分子链结合金属阳离子的能力允许在螺旋折叠和延伸线性状态之间产生缠绕/解缠绕过程。配位金属离子会产生大分子运动,通过与辅助配体络合剂竞争并通过连续的酸碱中和能量来实现其可逆性。将腙单元引入链中会赋予它们结构动态特性,从而通过组件交换实现不同链组成之间的相互转化。这些特性与纳米机械装置有关。我们展示了我们实验室开发的此类系统的形态和功能分析。

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