堆积
共价键
原位
二甲苯
调制(音乐)
材料科学
化学
化学工程
共价有机骨架
工作(物理)
邻二甲苯
结构异构体
光化学
结晶学
对二甲苯
组合化学
分子
选择性
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
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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