首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Self-Assembly of Calix[4]arene-Based Amphiphiles Bearing Polyethylene Glycols: Another Example of 'Platonic Micelles'
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Self-Assembly of Calix[4]arene-Based Amphiphiles Bearing Polyethylene Glycols: Another Example of 'Platonic Micelles'

机译:CALIX [4]亚苯基两种轴承聚乙二醇的自组装:另一个例子“柏拉米胶束”

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The aggregation number of classical micelles exhibits a certain distribution, which is a recognizable feature of conventional micelles. However, we recently identified perfectly monodisperse calix[4]arene-based micelles whose aggregation numbers agree with the vertex numbers of regular polyhedra, that is, Platonic solids, and thus they are named Platonic micelles. Regarding our hypothesis of the formation mechanism of Platonic micelles, both repulsive interactions including steric hindrance and electrostatic repulsions among the headgroups are important for determining their aggregation number; however, neither of these is necessarily needed to consider. In this study, we employed polyethylene glycols (PEGs) as the nonionic headgroup of calix[4]arene-based amphiphiles to study the effects of only repulsive interactions caused by steric hindrance on the formation of Platonic micelles. The amphiphiles containing relatively low-molecular-weight PEGs (550 or 1000 g mol(-1)) form dodecamer or octamer micelles, respectively, with no variation in the aggregation number. However, relatively high-molecular-weight PEGs (2000 g mol(-1)) produce polydispersed micelles with a range of aggregation number. PEG 2000 exhibits a greater affinity for water than PEG 550 and 1000, resulting in fewer hydrophobic interactions in micelle formation, as indicated by the drastic increase of the critical micelle concentration (CMC) value in the PEG 2000 system. The instability of the structure of PEG(2k)CaL5 micelles might contribute to the higher mobility of PEG in the micellar shell, resulting in a non-Platonic aggregation number with polydispersity.
机译:经典胶束的聚集数表现出一定的分布,这是常规的微胶粒的可识别的特征。然而,我们最近发现完美的单分散杯[4]芳烃为基础的胶束,其聚集数以正多面体,也就是柏拉图固体的顶点编号一致,因此,它们被命名为柏拉图胶束。关于我们的柏拉图式的胶束的形成机制假说,既排斥相互作用,包括空间位阻和头基团之间的静电排斥是决定其聚集一些重要的;然而,这些都不是一定需要考虑的问题。在这项研究中,我们采用聚乙二醇(PEG)作为杯的非离子头部基团[4]芳烃的基于两亲物来研究仅在柏拉图胶束的形成所造成的立体位阻排斥力的相互作用的影响。含有相对低分子量的PEG(550或千克摩尔(-1))的形式或十二聚体八聚体胶束,分别与在所述集合数没有变化的两亲物。然而,相对高的分子量的PEG(2000克摩尔(-1))产生具有一定范围的聚集数多分散胶束。 PEG 2000件展品由临界胶束浓度(CMC)值在PEG 2000系统中的急剧增加所指示的为水比PEG 550和1000具有更大的亲和力,导致胶束形成较少的疏水性相互作用,。 PEG(2K)的结构的不稳定CaL5胶束可能有助于PEG的更高的迁移率在胶束壳,导致与多分散性的非柏拉图聚合数。

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