微型多孔材料
亚胺
三苯胺
共价键
二氧化碳
吸附
离域电子
化学
纳米笼
单体
共价有机骨架
动态共价化学
有机化学
化学工程
材料科学
高分子化学
聚合物
分子
催化作用
超分子化学
工程类
作者
Zhitao Wang,Yanju Huang,Hui Li,Xiumei Li
标识
DOI:10.1016/j.micromeso.2022.112419
摘要
In recent years, many environmental problems including global warming and climate change have emerged due to the excessive emission of carbon dioxide. Covalent organic frameworks (COFs) exhibit good porosity and excellent stability. They can be constructed into uniform channel and tunable skeleton which are ideal for gas uptake. Here, we designed two new imine-linked COFs (ESM-COF-1 and ESM-COF-2) by condensation of two C3 symmetrical monomers. Interestingly, ESM-COF-1 and ESM-COF-2 displayed microporous features because of short length building units employed, the pore size, which is much smaller than most two-dimensional (2D) imine COFs. This virtue is good for gas adsorption via pore surroundings. Furthermore, rich methoxy units as electron-donate units on the walls delocalized electronic clouds from building units to the imine bond through π-conjugation interaction, indicating outstanding stability in harsh conditions. High-density active units from walls (triphenylamine and methoxy groups) to the imine linkage also improved the gas adsorption via the weak interaction. Interestingly, ESM-COFs exhibited stability, microporous features, and active units from walls to linkage to give a high carbon dioxide uptake at 4.64 mmol g−1, which is the excellent one among the reported 2D COFs.
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