单体
两亲性
材料科学
聚合物
超分子化学
自组装
空气水
化学工程
极地的
化学物理
高分子化学
化学
纳米技术
分子
有机化学
共聚物
复合材料
工程类
物理
机械
天文
作者
Arthur H. G. David,Mari C. Mañas‐Torres,Marcos D. Codesal,Irene López‐Sicilia,María T. Martín‐Romero,Luis Camacho,Juan M. Cuerva,Víctor Blanco,Juan J. Giner‐Casares,Luı́s Álvarez de Cienfuegos,Araceli G. Campaña
标识
DOI:10.1021/acs.joc.3c01854
摘要
We report the synthesis of a new set of amphiphilic saddle-shaped heptagon-containing polycyclic aromatic hydrocarbons (PAHs) functionalized with tetraethylene glycol chains and their self-assembly into large two-dimensional (2D) polymers. An in-depth analysis of the self-assembly mechanism at the air/water interface has been carried out, and the proposed arrangement models are in good agreement with the molecular dynamics simulations. Quite remarkably, the number and disposition of the tetraethylene glycol chains significantly influence the disposition of the PAHs at the interface and conditionate their packing under pressure. For the three compounds studied, we observed three different behaviors in which the aromatic core is parallel, perpendicular, and tilted with respect to the water surface. We also show that these curved PAHs are able to self-assemble in solution into remarkably large sheets of up to 150 μm2. These results show the relationship, within a family of curved nanographenes, between the monomer configuration and their self-assembly capacity in air/water interfaces and organic-water mixtures.
科研通智能强力驱动
Strongly Powered by AbleSci AI