二氯甲烷
乙腈
溶剂
背景(考古学)
选择性
聚合物
化学
二甲苯
结晶
萘
多孔性
高分子化学
化学工程
有机化学
材料科学
苯
催化作用
工程类
古生物学
生物
作者
Timur Ashirov,Jaebum Lim,Alexandra Robles,Thamon Puangsamlee,Patrick Fritz,Aurélien Crochet,Xiqu Wang,C. W. Hewson,Paul Lacomi,Ognjen Š. Miljanić,Ali Coskun
标识
DOI:10.1002/anie.202423809
摘要
The recovery and separation of organic solvents is highly important for the chemical industry and environmental protection. In this context, porous organic polymers (POPs) have significant potential owing to the possibility of integrating shape‐persistent macrocyclic units with high guest selectivity. Here, we report the synthesis of a macrocyclic porous organic polymer (np‐POP) and the corresponding model compound by reacting cyclotetrabenzil naphthalene octaketone macrocycle with 1,2,4,5‐tetraaminobenzene and 1,2‐diaminobenzene, respectively, under solvothermal conditions. Co‐crystallization of the macrocycle and the model compound with various solvent molecules revealed their size‐selective inclusion within the macrocycle. Building on this finding, the np‐POP with a hierarchical pore structure and a surface area of 579 m² g−1 showed solvent uptake strongly correlated with their kinetic diameters. Solvents with kinetic diameters below 0.6 nm—such as acetonitrile and dichloromethane—showed high uptake capacities exceeding 7 mmol g−1. Xylene separation tests revealed a high overall uptake (~34 wt%), with o‐xylene displaying a significantly lower uptake (~10 wt% less than other isomers), demonstrating the possibility of size and shape selective separation of organic solvents.
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