化学
共价键
堆积
蒽
位阻效应
量子纠缠
荧光
氢键
共价有机骨架
分子
纳米技术
化学物理
结晶学
光化学
立体化学
有机化学
光学
物理
材料科学
量子力学
量子
作者
Yuanpeng Cheng,Junjie Xin,Libang Xiao,Xuejiao Wang,Xu Zhou,Danyang Li,Bo Gui,Junliang Sun,Cheng Wang
摘要
Herein, we report the introduction of steric hindrance in molecular building blocks to prevent π···π stacking, thus allowing two-dimensional (2D) covalent organic sheets to form three-dimensional (3D) covalent organic frameworks (COFs) through entanglement. Starting from the rationally designed precursors containing a bulky anthracene unit in the vertical direction, a highly crystalline COF (3D-An-COF) was successfully synthesized. Very interestingly, 3D-An-COF was determined as an entangled 2D square net (sql) structure, and the high-resolution data (1.1 Å) obtained by the continuous rotation electron diffraction technique allowed us to directly locate all non-hydrogen atoms. Structurally, the presence of an anthracene group outside the C2h symmetry plane strongly reduces the π···π interactions and promotes the formation of square entanglements. In addition, 3D-An-COF is fluorescent and can be used as a sensor to detect the trace amount of antibiotics in water. This study provides a new strategy for the structural diversification of 3D COFs and will certainly motivate us to construct more entangled COFs for interesting applications in the future.
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