机械化学
材料科学
多孔性
拉曼光谱
结晶度
化学工程
共价键
纳米技术
化学
有机化学
光学
物理
工程类
复合材料
作者
Sebastian T. Emmerling,Luzia S. Germann,Patrick Julien,Igor Moudrakovski,Martin Etter,Tomislav Friščić,Robert E. Dinnebier,Bettina V. Lotsch
出处
期刊:Chem
[Elsevier]
日期:2021-05-14
卷期号:7 (6): 1639-1652
被引量:69
标识
DOI:10.1016/j.chempr.2021.04.012
摘要
Summary Covalent organic frameworks (COFs) have emerged as a new class of molecularly precise, porous functional materials characterized by broad structural and chemical versatility, with a diverse range of applications. Despite their increasing popularity, fundamental aspects of COF formation are poorly understood, lacking profound experimental insights into their assembly. Here, we use a combination of in situ X-ray powder diffraction and Raman spectroscopy to elucidate the reaction mechanism of mechanochemical synthesis of imine COFs, leading to the observation of key reaction intermediates that offer direct experimental evidence of framework templating through liquid additives. Moreover, the solid-state catalyst scandium triflate is instrumental in directing the reaction kinetics and mechanism, yielding COFs with crystallinity and porosity on par with solvothermal products. This work provides the first experimental evidence of solvent-based COF templating and is a significant advancement in mechanistic understanding of mechanochemistry as a green route for COF synthesis.
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