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在正离子表面活性剂-胆固醇和两性离子表面活性剂-胆固醇体系中,在己烷/水界面的薄膜形成和分子堆积。

Condensed Film Formation and Molecular Packing in Cationic Surfactant-Cholesterol and Zwitterionic Surfactant-Cholesterol Systems at the Hexane/Water Interface.

机构信息

Department of Chemistry, Faculty of Science, Kyushu University, Fukuoka 819-0395, Japan.

Faculty of Arts and Science, Kyushu University, Fukuoka 819-0395, Japan.

出版信息

J Phys Chem B. 2020 Oct 15;124(41):9275-9282. doi: 10.1021/acs.jpcb.0c07874. Epub 2020 Sep 30.

DOI:10.1021/acs.jpcb.0c07874
PMID:32997501
Abstract

A condensed film formation of surfactants with a charged head group at the oil/water interface was achieved by mixing surfactants of different geometric shapes to control molecular packing at the interface. The adsorbed films of mixed tetradecyltrimethylammonium bromide (C14TAB)-cholesterol (Chol) and tetradecylphosphocholine (C14PC)-Chol systems at the hexane/water interface were examined by interfacial tension and X-ray reflectivity measurements. The interfacial tension versus Chol concentration curves have break points because of the expanded-condensed phase transition of the adsorbed film. A two dimensional (2D) phase diagram, phase diagram of adsorption, indicated that 1:1 mixing in the condensed film is energetically favorable because of stronger mutual interaction between different molecules than between the same ones. The electron density profile normal to the interface manifested that the packing of C14TAB (or C14PC) and Chol molecules is like a 2D solid in the condensed state. As C14TAB and C14PC molecules take a corn shape with a large head group (critical packing parameter: CPP ≈ 1/3) and Chol takes an inverted corn shape with a bulky sterol ring (CPP > 1), the mixing of corn shape and inverted corn shape molecules produces well-ordered packing to promote solid-like molecular packing at the interface by energy gain because of vdW interaction between hydrophobic chains in addition to attractive ion-dipole interaction between head groups. Furthermore, the heterogeneous feature in the adsorbed film of the C14TAB-Chol system is explained by an interplay between contact energy and dipole interaction, which contribute to line tension at the domain boundary.

摘要

通过混合具有不同几何形状的表面活性剂来控制界面处的分子堆积,可以在油/水界面上实现带电荷头基的表面活性剂的浓缩成膜。通过界面张力和 X 射线反射率测量,研究了混合十四烷基三甲基溴化铵(C14TAB)-胆固醇(Chol)和十四烷基磷酸胆碱(C14PC)-Chol 体系在正己烷/水界面上的吸附膜。由于吸附膜的扩展-凝聚相转变,界面张力与 Chol 浓度曲线具有转折点。二维(2D)吸附相图表明,由于不同分子之间的相互作用强于相同分子之间的相互作用,在浓缩膜中 1:1 混合在能量上是有利的。垂直于界面的电子密度分布表明,C14TAB(或 C14PC)和 Chol 分子的堆积在凝聚态下类似于二维固体。由于 C14TAB 和 C14PC 分子具有较大的头基(临界堆积参数:CPP≈1/3),呈玉米状,而 Chol 分子呈倒玉米状,具有庞大的固醇环(CPP>1),因此玉米状和倒玉米状分子的混合产生有序堆积,通过范德华相互作用(除了头基之间的吸引离子偶极相互作用)获得能量增益,从而促进界面处的固体状分子堆积。此外,C14TAB-Chol 体系吸附膜的不均匀性可以通过接触能和偶极相互作用之间的相互作用来解释,这有助于在畴界处产生线张力。

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