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无氟柱[5]芳烃与全氟二酸在全水界面的二维和三维自组装

2D and 3D Self-Assembly of Fluorine-Free Pillar-[5]-Arenes and Perfluorinated Diacids at All-Aqueous Interfaces.

作者信息

Honaker Lawrence W, Gao Tu-Nan, de Graaf Kelsey R, Bogaardt Tessa V M, Vink Pim, Stürzer Tobias, Kociok-Köhn Gabriele, Zuilhof Han, Miloserdov Fedor M, Deshpande Siddharth

机构信息

Laboratory of Physical Chemistry and Soft Matter, Wageningen University & Research, Wageningen, 6708 WE, The Netherlands.

Laboratory of Organic Chemistry, Wageningen University & Research, Wageningen, 6708 WE, The Netherlands.

出版信息

Adv Sci (Weinh). 2024 Aug;11(29):e2401807. doi: 10.1002/advs.202401807. Epub 2024 May 24.

Abstract

The interaction of perfluorinated molecules, also known as "forever chemicals" due to their pervasiveness, with their environment remains an important yet poorly understood topic. In this work, the self-assembly of perfluorinated molecules with multivalent hosts, pillar-[5]-arenes, is investigated. It is found that perfluoroalkyl diacids and pillar-[5]-arenes rapidly and strongly complex with each other at aqueous interfaces, forming solid interfacially templated films. Their complexation is shown to be driven primarily by fluorophilic aggregation and assisted by electrostatic interactions, as supported by the crystal structure of the complexes, and leads to the formation of quasi-2D phase-separated films. This self-assembly process can be further manipulated using aqueous two-phase system microdroplets, enabling the controlled formation of 3D micro-scaffolds.

摘要

全氟分子,因其无处不在也被称为“永久化学物质”,与它们所处环境之间的相互作用仍是一个重要但尚未得到充分理解的课题。在这项工作中,研究了全氟分子与多价主体柱[5]芳烃的自组装过程。研究发现,全氟烷基二酸与柱[5]芳烃在水界面处迅速且强烈地相互络合,形成固体界面模板化薄膜。配合物的晶体结构表明,它们的络合主要由亲氟聚集驱动,并受静电相互作用辅助,进而形成准二维相分离薄膜。这种自组装过程可通过水相双系统微滴进一步调控,从而实现三维微支架的可控形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f92d/11304270/da30bef2d90a/ADVS-11-2401807-g002.jpg

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