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探索多组分低分子量凝胶剂的可调光学和机械性能。

Exploring the Tunable Optical and Mechanical Properties of Multicomponent Low-Molecular-Weight Gelators.

作者信息

Loos Jeanette N, Boott Charlotte E, Hayward Dominic W, Hum Gabriel, MacLachlan Mark J

机构信息

Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia V6T 1Z1, Canada.

Jülich Centre for Neutron Science, Forschungszentrum Jülich GmbH, Outstation at MLZ, Lichtenbergstraße 1, Garching 85747, Germany.

出版信息

Langmuir. 2021 Jan 12;37(1):105-114. doi: 10.1021/acs.langmuir.0c02464. Epub 2021 Jan 3.

DOI:10.1021/acs.langmuir.0c02464
PMID:33393307
Abstract

A class of amino acid-based low-molecular-weight gelators (LMWGs) was used for single and multicomponent gel studies to investigate their tunable optical properties and their self-assembly process. The optical properties of multicomponent gels were found to be easily tuned by changing the proportion of the components, varying from opaque to highly transparent gels as analyzed using ultraviolet-visible spectroscopy. This phenomenon allows tunability without introducing another variable into the system. Scanning electron microscopy, differential scanning calorimetry, and small-angle X-ray scattering (SAXS) were used to investigate the structures of the gels. It was found that because of the structural similarities of the molecules, the gelators favor coassembly packing over self-sorting. The emergence of transparency was ascribed to changes in the fiber diameters. Moreover, analysis of the SAXS data allowed us to compare the molecular order present in the gel phase with single-crystal X-ray diffraction (SCXRD) data. Our analysis suggests that the packing of molecules seen in the crystalline phase is translated into the gel network. This reveals that the structure of the crystalline phase seen through SCXRD is a useful tool to aid in understanding the molecular packing in the gel phase.

摘要

一类基于氨基酸的低分子量凝胶剂(LMWGs)被用于单组分和多组分凝胶研究,以探究其可调谐光学性质及其自组装过程。通过紫外可见光谱分析发现,多组分凝胶的光学性质可通过改变组分比例轻松调节,从不透明凝胶到高度透明凝胶变化多样。这种现象使得在不向系统引入另一个变量的情况下实现可调谐性。使用扫描电子显微镜、差示扫描量热法和小角X射线散射(SAXS)来研究凝胶的结构。发现由于分子的结构相似性,凝胶剂更倾向于共组装堆积而非自分类。透明度的出现归因于纤维直径的变化。此外,对SAXS数据的分析使我们能够将凝胶相中的分子有序性与单晶X射线衍射(SCXRD)数据进行比较。我们的分析表明,在晶相中观察到的分子堆积转化为凝胶网络。这表明通过SCXRD观察到的晶相结构是有助于理解凝胶相中分子堆积的有用工具。

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