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Formation of heat-triggered supramolecular organogel in which β-cyciodextrin as sole gelator

机译:以β-环糊精为唯一胶凝剂的热触发超分子有机凝胶的形成

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摘要

β-Cyclodextrins (β-CDs), without the help of the guest molecules embedding in cavities, can self-assemble an organogel with a very small amount of lithium chloride (LiCl) in N,N-dimethylformamide (DMF). Microstructures of the organogel were confirmed to be β-CD molecular clusters composed of many channel-type β-CD fibers extending from a cage-type β-CD core in various directions. The process of the gel formation and the structure were suggested based on FTIR, TR-FTIR, 1H NMR and XRD results. The interactions of the various molecules in the system were discussed for gelation. The morphology of the organogel was characterized by OM and SEM. A molecular dynamics simulation of the gel structure was performed in agreement with the results. In addition, the concentration of β-CD for the gel formation ranged from 0.13 to 0.28mol/L. The approximate heat effect of the phase transition was 28 kJ/mol. This investigation will be of great significance to develop new temperature-controlling materials with native β-CD of low cost in application.
机译:β-环糊精(β-CDs)无需借助嵌入腔中的客体分子,就可以在N,N-二甲基甲酰胺(DMF)中用非常少量的氯化锂(LiCl)自组装有机凝胶。确认有机凝胶的微结构是由许多从笼型β-CD核向各个方向延伸的通道型β-CD纤维组成的β-CD分子簇。根据FTIR,TR-FTIR,1H NMR和XRD结果,提出了凝胶的形成过程和结构。讨论了系统中各种分子的相互作用以进行凝胶化。通过OM和SEM表征有机凝胶的形态。与结果一致地进行了凝胶结构的分子动力学模拟。另外,用于凝胶形成的β-CD的浓度为0.13至0.28mol / L。相变的近似热效应为28kJ / mol。该研究对于开发应用成本低的天然β-CD新型控温材料具有重要意义。

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