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基于杯[4]芳烃的柏拉图式胶束的结构分析。

Structural analysis of a calix[4]arene-based Platonic Micelle.

作者信息

Mylonas Efstratios, Yagi Naoto, Fujii Shota, Ikesue Kodai, Ueda Tomoya, Moriyama Hideaki, Sanada Yusuke, Uezu Kazuya, Sakurai Kazuo, Okobira Tadashi

机构信息

Japan Synchrotron Radiation Research Institute (JASRI/SPring-8), 1-1-1, Kouto, Sayo-cho, Sayo-gun, Hyogo, 679-5198, Japan.

Department of Chemical Processes and Environments, Faculty of Environmental Engineering, The University of Kitakyushu, 1-1, Hibikino, Wakamatsu-ku, Kitakyushu, 808-0135, Japan.

出版信息

Sci Rep. 2019 Feb 13;9(1):1982. doi: 10.1038/s41598-018-38280-1.

Abstract

We have recently introduced the concept of "Platonic micelles", the preference of spherical micelles to specific aggregation numbers mostly coinciding with the number of faces of platonic solids. This effect was observed on bulky, mostly calix[4]arene-based surfactant systems with small aggregation numbers. The preferred aggregation numbers result in better sphere coverage, highliting the packing and the "protection" of hydrophobic cores from the aqueous solvent as the most important factor for this preference. In the present study we further explore the interactions that drive the packing of the highly charged PACaL3 surfactant into highly symmetrical hexameric micelles. We performed a series of molecular dynamics simulations that yielded a large set of structures and an ensemble in good agreement with the experimental Small Angle X-ray Scattering data was selected. The geometry and the rigidity of the calix[4]arene group with proper tail length and headgroup volume are the driving forces for the high symmetry and monodispersity of the micelle. The charge of the headgroups is mainly responsible for inhibiting the formation of higher order structures. Sodium, shown to be important for the stability of the micelle, is not directly interacting with the micelle implying that the calix[4]arene ring is a C2ν symmetry conformation.

摘要

我们最近引入了“柏拉图式胶束”的概念,即球形胶束对特定聚集数的偏好,这些聚集数大多与柏拉图立体的面数一致。这种效应在具有小聚集数的、大多基于杯[4]芳烃的庞大表面活性剂体系中被观察到。优选的聚集数导致更好的球体覆盖,突出了堆积以及疏水核与水性溶剂的“隔离”是这种偏好的最重要因素。在本研究中,我们进一步探索了驱动高电荷PACaL3表面活性剂堆积成高度对称的六聚体胶束的相互作用。我们进行了一系列分子动力学模拟,得到了大量结构,并选择了与实验小角X射线散射数据高度一致的一个系综。具有适当尾长和头基体积的杯[4]芳烃基团的几何形状和刚性是胶束高对称性和单分散性的驱动力。头基的电荷主要负责抑制高阶结构的形成。已证明钠对胶束的稳定性很重要,但它不直接与胶束相互作用,这意味着杯[4]芳烃环是C2ν对称构象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba05/6374510/8647fbd872d8/41598_2018_38280_Fig1_HTML.jpg

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