Phytantriol and monoolein in aqueous deep eutectic solvent and protic ionic liquid solutions.

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL
Karen J Edler, Gregory G Warr, Alexander M Djerdjev, Minh Thu Lam, Adrian M Hawley, Stephen Mudie
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引用次数: 0

Abstract

Lyotropic liquid crystal gels of phytantriol and monoolein are well known examples of self-assembled systems in water, which have multiple applications across biomedical and materials science. However aqueous systems can be restricted by rapid solvent evaporation, and the limited solubility of some species in water. Here we explore the formation of liquid crystalline phases of phytantriol and monoolein in mixtures of water with two protic ionic liquids, ethylammonium nitrate (EAN) and ethanolammonium nitrate (EtAN), and three deep eutectic solvents (DES) formed from mixtures of choline chloride with urea, fructose or citric acid. The structures of the gel phase in excess solvent were measured using small angle X-ray scattering for a fixed lipid concentration (5% w/w) as a function of temperature. The phase diagrams of both lipids in DES-water mixtures and the non-amphiphilic ionic liquid, EtAN, indicate that higher negative curvature inverse hexagonal structures are favoured by addition of water. However, the amphiphilic ionic liquid EAN swells and stabilises the cubic Pn3m structure. The interplay of solvent structure, polarity and molecular size are key to understanding the formation and stability of lyotropic liquid crystalline gels in these systems.

植物三醇和单油在深共熔溶剂和质子离子液体中的应用。
植物三醇和单油醇的溶性液晶凝胶是众所周知的水中自组装系统的例子,在生物医学和材料科学中有多种应用。然而,由于溶剂的快速蒸发和某些物质在水中的溶解度有限,水性体系可能受到限制。在这里,我们探索了植物三醇和单油在水与两种质子离子液体(硝酸乙铵(EAN)和乙醇硝酸铵(EtAN))的混合物中液晶相的形成,以及三种由氯化胆碱与尿素、果糖或柠檬酸的混合物形成的深共晶溶剂(DES)。在固定脂质浓度(5% w/w)随温度变化的条件下,采用小角x射线散射法测量了凝胶相在过量溶剂中的结构。des -水混合物和非两亲性离子液体EtAN的相图表明,水的加入有利于高负曲率逆六边形结构的形成。然而,两亲性离子液体EAN膨胀并稳定立方Pn3m结构。溶剂结构、极性和分子大小的相互作用是了解这些体系中溶致液晶凝胶形成和稳定性的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Faraday Discussions
Faraday Discussions 化学-物理化学
自引率
0.00%
发文量
259
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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