选择性
共价有机骨架
化学
共价键
亚胺
结构异构体
吸附
三键
反向
计算化学
工作(物理)
乙烯
选择性吸附
冷凝
双键
金属有机骨架
立体化学
连接器
有机化学
光化学
顺反异构
作者
Baoqiu Yu,Tonghai Wang,Yucheng Jin,Zhongwei Liu,Qingmei Xu,Shangwei Yuan,Xin Xiao,Xu Ding,Hailong Wang,Zhenjie Zhang,Banglin Chen,Jianzhuang Jiang
摘要
ABSTRACT Constructing triple framework isomerism with atom‐resolution structures is of great significance but remains highly challenging for covalent organic frameworks (COFs). Herein, [3+3] imine condensation of 1,3,5‐trimethyl‐2,4,6‐tris(4‐aminophenyl)benzene with 1,3,5‐triethyl‐2,4,6‐tris(4‐formylphenyl)benzene affords three single‐crystal COF isomers composed of hcb nets. Their AB hcb stacking, double [2D+2D], and triple [2D+2D+2D] crossing entangled structures have been resolved by 3D electron diffraction. Among the three desolvated COFs, GZU‐4a exhibits the highest ethane uptake (100.7 cm 3 g −1 ) and ethane/ethylene selectivity (1.6), enabling one‐step production of high‐purity ethylene (>99.99%) in dynamic breakthrough experiments. The superior and inverse separation performance originates from its rigid non‐interpenetrated framework with optimized pore confinement for strengthened ethane binding. This work not only presents an unprecedented example of triple isomeric COFs with atom‐resolution structures from non‐interpenetration to inclined interpenetration of 2D nets, but also shows an inverse adsorption selectivity for ethane over ethylene, greatly enriching the diversity of COFs.
科研通智能强力驱动
Strongly Powered by AbleSci AI