范德瓦尔斯力
纳米技术
非共价相互作用
共价键
氢键
材料科学
化学
有机化学
分子
作者
Pei Huang,Lu‐Hua Hou,Mingyi Yang,Cheng Xiao,Yanli Wu,Si‐Jing Cai,Wenjie Guo,Mi Zhang,Meng Lu,Ya‐Qian Lan
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-05-12
卷期号:64 (29): e202507002-e202507002
被引量:29
标识
DOI:10.1002/anie.202507002
摘要
As an important branch of the covalent organic frameworks (COFs) family, one-dimensional COFs (1D COFs), which are formed by the ordered arrangement of confined covalent bonds in one dimension and non-covalent interactions (van der Waals force, π-π interactions, and hydrogen bonds) in the vertical two and three dimensions has aroused much attention. Compared with two-dimensional (2D)/three-dimensional (3D) COFs, 1D COFs behaved more easily dispersing and had more opportunities for active sites exposure due to their weaker interchain/interlayer interaction, modified nonlinear edge, and pore structures. These features make them have great application potential in many fields, including catalysis, energy storage, adsorption, sensing, and others. In this minireview, we highlight the state-of-the-art advances of 1D COFs in the structure design principles of building blocks, synthesis strategies, and their related applications. Furthermore, we present an in-depth outlook on the challenges and opportunities faced by 1D COFs, aiming to offer insights for future studies in this intriguing and significant research field.
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