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Hydrogen-Bonding-Regulated Supramolecular Nanostructures and Impact on Multivalent Binding

机译:氢键合调节的超分子纳米结构和对多价结合的影响

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摘要

Herein we describe the H-bonding-regulated nanostructure, thermodynamics, and multivalent binding of two bolaamphiphiles NDI-1 and NDI-2 consisting of a hydrophobic naphthalene diimide connected to a hydrophilic wedge by a H-bonding group and a glucose moiety on its two arms. NDI-1 and NDI-2 differ by the single H-bonding group, namely, hydrazide or amide, which triggers the formation of vesicles and cylindrical micelles, respectively. Although the extended H-bonding ensures stacking with head-to-head orientation and the formation of an array of the appended glucose moieties in both systems, the adaptive cylindrical structure exhibited superior multivalent binding with concanavalinA (ConA) to that of the vesicle. A control amphiphile lacking a H-bonding group assembled with a random lateral orientation to produce spherical micelles without any notable multivalent binding.
机译:在此,我们描述了由H键合基团连接到亲水性楔形的疏水性萘二亚胺和其两者的疏水性萘二亚胺组成的H键合调节的纳米结构,热力学和多价结合 武器。 NDI-1和NDI-2因单个H键合基团,即酰肼或酰胺而异,其触发囊泡和圆柱形胶束的形成。 尽管延伸的H键合确保堆叠头部到头方向,并且在两个系统中形成一系列所附葡萄糖部分,自适应圆柱形结构与囊泡的康尼韦娜(Cona)表现出优异的多价结合。 缺少具有随机横向取向的H键合组的对照两亲物,以产生球形胶束而没有任何显着的多价结合。

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