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通过配位相互作用实现的平面薄片和螺旋管之间的超分子开关。

Supramolecular switching between flat sheets and helical tubules triggered by coordination interaction.

机构信息

Department of Chemistry, Seoul National University, Seoul 151-747, Korea.

出版信息

J Am Chem Soc. 2013 Feb 13;135(6):2156-9. doi: 10.1021/ja400160j. Epub 2013 Jan 31.

Abstract

Here we report the spontaneous formation of switchable sheets in aqueous solution, which is based on bent-shaped aromatic amphiphiles containing m-pyridine units at the terminals and a hydrophilic dendron at the apex. The aromatic segments self-assemble into flat sheets consisting of a zigzag conformation through π-π stacking interactions. Notably, the sheets reversibly transform into helical tubules at higher concentration and into discrete dimeric macrocycles at a lower concentration in response to Ag(I) ions through reversible coordination interactions between the pyridine units of the aromatic segments and the Ag(I) ions. While maintaining the coordination bonding interactions, the helical tubules reversibly transform into the dimeric macrocycles in response to the variation in concentration.

摘要

在这里,我们报告了在水溶液中自发形成的可切换片,它基于含有 m-吡啶单元在末端和亲水树枝状大分子在顶点的弯曲形状的芳香族两亲分子。芳香族片段通过π-π堆积相互作用自组装成由锯齿构象组成的平板片。值得注意的是,这些片在较高浓度下可逆地转化为螺旋管,在较低浓度下转化为离散的二聚大环,这是由于芳香族片段的吡啶单元与 Ag(I)离子之间的可逆配位相互作用。在保持配位键相互作用的同时,螺旋管也能响应浓度的变化而可逆地转化为二聚大环。

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