堆积
共价键
原位
溶剂
二甲苯
材料科学
化学
有机化学
苯
作者
Xuhan Zheng,Hui Liu,Jialin Cui,Yuxia Guo,Hongze Xu,Zejun Zhang,Jianming Zhang,Yingjie Zhao
标识
DOI:10.1002/anie.202519150
摘要
Abstract The precise regularity of stacking modes in two‐dimensional covalent organic frameworks (2D COFs) remains insufficiently understood, and achieving precise control during synthesis is highly challenging. Here, we show that the interlayer stacking arrangement can be in situ modulated simply by varying the reaction solvent, allowing the selective formation of either eclipsed (AA) or staggered (AB) stacking. This direct solvent‐driven regulation, achieved without post‐synthetic modification, underscores the dynamic nature of COF assembly. Notably, the AA‐stacked COF exhibits promising separation performance for xylene isomers compared to its AB‐stacked counterpart.
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