Assembly of Dumbbell- and Bola-Shaped Amphiphiles: Vesicles with Condensed Hydrophobic Domains or Blackberry-type Structures with Porous Surfaces?

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Xiaohan Xu, Jiayingzi Wu, Zhiwei Lin, Abdol Hadi Mokarizadeh, Xing-han Li, Mesfin Tsige*, Stephen Z. D. Cheng* and Tianbo Liu*, 
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Abstract

Dumbbell- and bola-shaped amphiphiles are commonly expected to self-assemble into vesicles with condensed hydrophobic domains due to the dominant hydrophobic interaction. In this work, we examined the assemblies of the dumbbell-shaped AC60-AC60 amphiphile, with two carboxylic acid-functionalized fullerenes (AC60) polar head groups linked by an organic tether, and found that they assemble into hollow, spherical blackberry-type structures with porous surfaces, judged by their smaller assemblies in organic solvents with higher polarity and in aqueous solutions with high pH. We attribute the formation of blackberry structures to the organic tether that may be too short to fill up a condensed hydrophobic domain, as confirmed by all-atom simulations. This is further proved by noticing that several bola-type macromolecules with hydrophilic polyethylene glycol (PEG) chain being the linker and no hydrophobic components, AC60-PEG-AC60, can also self-assemble into hollow, spherical assemblies and demonstrate similar pH response as the assemblies from AC60-AC60 dumbbells. Therefore, we conclude that the driving force of the self-assembly for these dumbbell- or bola-shaped molecules is counterion-mediated attraction from the two AC60 head groups rather than the hydrophobic interaction due to the organic linkers. The so-formed blackberry structures here, as well-studied before in other systems, possess porous surfaces, making these charged amphiphiles a valuable model for designing stable nanocontainers with controllable porosity to the change of the environment.

Abstract Image

Abstract Image

哑铃形和波拉形双亲化合物的组装:具有凝结疏水域的囊泡还是具有多孔表面的黑莓型结构?
由于疏水作用占主导地位,哑铃形和波拉形双亲化合物通常会自组装成具有凝聚疏水结构域的囊泡。在这项工作中,我们研究了哑铃形 AC60-AC60 双亲化合物的组装情况,这种双亲化合物的两个羧酸官能化富勒烯(AC60)极性头基团通过有机系链连接在一起,我们发现,根据它们在极性较高的有机溶剂和高 pH 值水溶液中较小的组装量判断,它们组装成了具有多孔表面的中空球形黑莓型结构。我们将黑莓结构的形成归因于有机系链太短,无法填满凝结的疏水域,全原子模拟也证实了这一点。我们还注意到,以亲水性聚乙二醇(PEG)链为连接物、不含疏水成分的几种波拉型大分子(AC60-PEG-AC60)也能自组装成空心球形组装体,并表现出与 AC60-AC60 哑铃组装体相似的 pH 响应,从而进一步证明了这一点。因此,我们得出结论,这些哑铃状或棒状分子自组装的驱动力是两个 AC60 头基通过反离子介导的吸引力,而不是有机连接体产生的疏水相互作用。这里形成的黑莓结构与之前在其他系统中研究的结果一样,具有多孔的表面,使这些带电的双亲化合物成为设计具有可控孔隙率的稳定纳米容器以适应环境变化的宝贵模型。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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