位阻效应
配体(生物化学)
金属有机骨架
作文(语言)
领域(数学分析)
化学
控制(管理)
计算机科学
有机化学
数学
受体
哲学
数学分析
吸附
人工智能
生物化学
语言学
作者
Yiwen He,Mattheus De Souza,Tian‐Yi Luo,Siddarth K. Achar,J. Karl Johnson,Nathaniel L. Rosi
标识
DOI:10.1002/anie.202409150
摘要
Abstract Incorporating diverse components into metal–organic frameworks (MOFs) can expand their scope of properties and applications. Stratified MOFs (sMOFs) consist of compositionally unique concentric domains (strata), offering unprecedented complexity through partitioning of structural and functional components. However, the labile nature of metal‐ligand coordination handicaps achieving compositionally distinct domains due to ligand exchange reactions occurring concurrently with secondary strata growth. To achieve complex sMOF compositions, characterizing and controlling the competing processes of new strata growth and ligand exchange are vital. This work systematically examines controlling ligand exchange in UiO‐67 sMOFs by tuning ligand sterics. We present quantitative methods for assessing and visualizing the outcomes of strata growth and ligand exchange that rely on high‐angle annular dark‐field images and elemental mapping via scanning transmission electron microscopy‐energy dispersive X‐ray spectroscopy. In addition, we leverage ligand sterics to create ‘blocking layers’ that minimize ligand exchange between strata which are particularly susceptible to ligand exchange and inter‐strata ligand mixing. Finally, we evaluate strata compositional integrity in various solvents and find that sMOFs can maintain their compositions for >12 months in some cases. Collectively, these studies and methods enhance understanding and control over ligand placement in multi‐domain MOFs, factors that underscore careful tunning of properties and function.
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