吡嗪
共价键
等结构
吸附
单体
共价有机骨架
材料科学
化学工程
氮气
气体分离
金属有机骨架
羟醛缩合
分离(统计)
化学
纳米技术
冷凝
动态共价化学
选择性吸附
分离法
有机化学
比表面积
高分子化学
组合化学
作者
Mingshuan Yang,Shujie Qiao,Jinhua Wang,Pengzhong Shi,Zhiyong Guo
出处
期刊:Small
[Wiley]
日期:2026-01-12
卷期号:: e12337-e12337
标识
DOI:10.1002/smll.202512337
摘要
ABSTRACT Effective separation of C 2 H 2 /CO 2 is a daunting challenge due to their close molecular sizes and physical properties. Covalent organic frameworks (COFs) have recently attracted widespread attention in the fields of gas adsorption and separation owing to their high surface area and pore designability. In this work, three nitrogen‐rich vinylene‐linked isostructural COFs were constructed via Aldol condensation between tetratopic monomers containing pyrazine (PZ) groups and terephthalaldehyde. All three PZ‐COFs exhibited high specific surface area and decent chemical/thermal stability. Intriguingly, both their adsorption capacity of C 2 H 2 (from 57.7 to 107.2 cm 3 g −1 ) and the separation efficiency of C 2 H 2 /CO 2 increased along with the growing amount of PZ units within the three frameworks. Dynamic experimental breakthrough results and theoretical calculations further demonstrated that the high‐density nitrogen sites along the one‐dimensional channels of these COFs played the pivotal role in the C─H···N bond interactions toward C 2 H 2 molecules, which subsequently regulated their separation performance of C 2 H 2 /CO 2 mixtures.
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