Suppr超能文献

利用单一组分氟化树枝状两亲分子控制 stomatosomes 的自组装。

Controlled self-assembly of stomatosomes by use of single-component fluorinated dendritic amphiphiles.

机构信息

Forschungszentrum für Elektronenmikroskopie, Institut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstraße 36a, 14195 Berlin, Germany.

出版信息

Soft Matter. 2018 Jun 27;14(25):5256-5269. doi: 10.1039/c8sm00243f.

Abstract

A series of novel non-ionic amphiphiles with dendritic oligoglycerol head groups of different generations ([G1]-[G3]) and lipophilic/fluorophilic tail segments, comprising single or double tail alkyl chains, C8F17-perfluoro rod segments as well as flexible spacer groups of different lengths were designed and synthesized. We expected that the differences in the size of the dendritic head groups in combination with perfluorinated segments would have an impact on the supramolecular structures formed in aqueous solution if compared with the hydrogenated analogues. Investigating the self-assembly behavior mainly by cryogenic transmission electron microscopy (cryo-TEM) and cryo-electron tomography (cryo-ET) we found as a new result the formation of perforated bilayer vesicles (stomatosomes) and bicontinuous network structures. Surprisingly, we have observed stomatosome formation by self-assembly of single component fluorinated dendritic amphiphiles. These assembly structures turned out to be extremely robust against harsh conditions, although there are strong indications that they represent non-equilibrium structures, which eventually transform into a bicontinuous cubic network structure of double diamond symmetry. In general, the molecular asymmetry of amphiphiles tuned by chemical design induced the expected trend from spherical micelles through worm-like micelles to perforated bilayers and three-dimensional network structures.

摘要

一系列新型的非离子两亲性化合物具有不同代数的树枝状低聚糖甘油头部基团 ([G1]-[G3]) 和疏水性/亲氟性尾部片段,包括单尾或双尾烷基链、C8F17 全氟棒状段以及不同长度的柔性间隔基团。我们期望,与氢化类似物相比,树枝状头部基团的大小差异以及全氟部分的差异会对在水溶液中形成的超分子结构产生影响。通过低温透射电子显微镜 (cryo-TEM) 和低温电子断层扫描 (cryo-ET) 主要研究自组装行为,我们发现了一个新的结果,即形成了穿孔双层囊泡(穿孔囊泡)和双连续网络结构。令人惊讶的是,我们已经观察到由单一成分氟化树枝状两亲物自组装形成穿孔囊泡。这些组装结构非常坚固,能够抵抗恶劣条件,尽管有强烈的迹象表明它们代表非平衡结构,最终会转化为具有双重菱形对称性的双连续立方网络结构。总的来说,通过化学设计调节两亲分子的分子不对称性诱导了从球形胶束到蠕虫状胶束再到穿孔双层和三维网络结构的预期趋势。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验