Towards nanomaterials with tubular pores: synthesis and self-assembly of bis-pillar[5]arene

Q4 Materials Science
D. Shurpik, Yulia I. Aleksandrova, Lyaysan I. Makhmutova, Alan Akhmedov, Ivan I. Stoikov
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引用次数: 0

Abstract

Recently, materials obtained using supramolecular chemistry approaches, and, in particular, spatially preorganized macrocyclic compounds, have attracted close attention of the researchers. Pillar[n]arenes are of special interest due to their tubular spatial structure and macrocyclic cavity. A similar tubular structure is retained in the supramolecular packaging of pillar[5]arene crystals, forming pores. In this study, we developed a block synthetic approach for the preparation of bis-pillar[5]arene containing amide groups. The ability of the synthesized bis-pillar[5]arene to form stable self-associates in solvents of different polarity (CHCl3 and CH3OH) was demonstrated by the DLS method. In trichloromethane at concentration of 1·10–3 M, monodisperse associates with average hydrodynamic diameter of 227 nm (PDI = 0.28) are formed; in methanol, stable associates (1·10–6 M) have an average hydrodynamic diameter of 136 nm (PDI = 0.21). The results obtained can be used to create new supramolecular systems, molecular machines, or capture and detect various organic molecules. 
开发具有管状孔隙的纳米材料:双柱[5]炔的合成与自组装
近年来,利用超分子化学方法获得的材料,特别是空间预组织的大环化合物,引起了研究人员的密切关注。柱[n]芳烃由于其管状空间结构和大环空腔而受到特别关注。柱状[5]芳烃晶体的超分子包装中保留了类似的管状结构,形成孔隙。在本研究中,我们开发了一种嵌段合成方法来制备含酰胺基团的双柱[5]芳烃。DLS法证明了合成的双柱[5]芳烃在不同极性溶剂(CHCl3和CH3OH)中形成稳定自缔合物的能力。在浓度为1·10-3 M的三氯甲烷中,形成了平均水动力直径为227 nm (PDI = 0.28)的单分散缔合物;在甲醇中,稳定缔合物(1·10-6 M)的平均水动力直径为136 nm (PDI = 0.21)。获得的结果可用于创建新的超分子系统,分子机器,或捕获和检测各种有机分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chimica Techno Acta
Chimica Techno Acta Chemical Engineering-Chemical Engineering (all)
CiteScore
1.00
自引率
0.00%
发文量
67
审稿时长
4 weeks
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