离子键合
堆积
共价键
阳离子聚合
静电学
偶极子
化学物理
离子
材料科学
非共价相互作用
化学
纳米技术
分子
高分子化学
氢键
物理化学
有机化学
作者
Ning Huang,Ping Wang,Matthew A. Addicoat,Thomas Heine,Donglin Jiang
标识
DOI:10.1002/anie.201611542
摘要
Abstract Covalent organic frameworks (COFs) have emerged as a tailor‐made platform for designing layered two‐dimensional polymers. However, most of them are obtained as neutral porous materials. Here, we report the construction of ionic crystalline porous COFs with positively charged walls that enable the creation of well aligned yet spatially confined ionic interface. The unconventional reversed AA‐stacking mode alternately orientates the cationic centers to both sides of the walls; the ionic interface endows COFs with unusual electrostatic functions. Because all of the walls are decorated with electric dipoles, the uptake of CO 2 is enhanced by three fold compared to the neutral analog. By virtue of sufficient open space between cations, the ionic interface exhibits exceptional accessibility, efficiency, and selectivity in ion exchange to trap anionic pollutants. These findings suggest that construction of the ionic interface of COFs offers a new way to structural and functional designs.
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