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环糊精与弱阴离子型烷氧基羧酸盐包合物的温敏行为。

Thermoresponsive behavior of cyclodextrin inclusion complexes with weakly anionic alkyl ethoxy carboxylates.

机构信息

Dipartimento di Fisica e Chimica, Università degli Studi di Palermo, Viale delle Scienze pad 17, 90128, Palermo, Italy.

Institut Max von Laue-Paul Langevin, 71 avenue des Martyrs, 38042, Grenoble, France.

出版信息

Soft Matter. 2023 Feb 22;19(8):1523-1530. doi: 10.1039/d2sm01621d.

Abstract

This study investigates the temperature responsive behavior of inclusion complexes formed by weakly anionic alkyl ethoxy carboxylates and α (αCD) and β-cyclodextrins (βCD). Small-angle neutron scattering (SANS) was performed to probe the structural behaviour at the 1-100 nanometer scale of the hierarchical assemblies at different temperatures. The phase transitions and thermodynamics were systematically monitored as a function of the degree of ionization of the surfactant by differential scanning calorimetry (DSC). Herein, we investigate the effect of the surfactant degree of ionization on the thermoresponsive properties of the inclusion complex supramolecular assemblies. Inclusion complexes formed with the ionized surfactant spontaneously assemble into multilayered structures, which soften with increasing temperature. We also found that the presence of charges is not only required to impart order to the supramolecular assemblies, but also induced in-plane crystallization of the inclusion complexes. Finally, the use of a weakly anionic surfactant allows us to probe the interplay between the charge density and temperature on the assembly of surfactant-cyclodextrin inclusion complexes. This study helps to improve the design of multi-responsive supramolecular systems based on cyclodextrins.

摘要

本研究考察了弱阴离子型烷氧基羧酸酯与 α(αCD)和 β-环糊精(βCD)形成的包合物在温度响应行为。小角中子散射(SANS)用于探测在不同温度下的层次组装在 1-100 纳米尺度的结构行为。通过差示扫描量热法(DSC)系统地监测了表面活性剂的离解度对相转变和热力学的影响。在这里,我们研究了表面活性剂的离解度对包合物超分子组装体的热敏性能的影响。与离子化表面活性剂形成的包合物自组装成多层结构,随着温度的升高而软化。我们还发现,电荷的存在不仅需要赋予超分子组装有序性,而且还诱导包合物的面内结晶。最后,使用弱阴离子表面活性剂可以研究电荷密度和温度对表面活性剂-环糊精包合物组装的相互作用。本研究有助于改进基于环糊精的多响应超分子体系的设计。

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