共价键
化学
组合化学
共价有机骨架
多孔性
支柱
材料科学
分子识别
超分子化学
固态
纳米技术
分子
有机化学
结构工程
工程类
物理化学
作者
Lu Liu,Yueyun Hu,Shaofeng Huang,Yinghua Jin,Jingnan Cui,Weitao Gong,Wei Zhang
出处
期刊:Chemical Science
[The Royal Society of Chemistry]
日期:2021-01-01
卷期号:12 (40): 13316-13320
被引量:31
摘要
It is highly desirable to maintain both permanent accessible pores and selective molecular recognition capability of macrocyclic cavitands in the solid state. Integration of well-defined discrete macrocyclic hosts into ordered porous polymeric frameworks (e.g., covalent organic frameworks, COFs) represents a promising strategy to transform many supramolecular chemistry concepts and principles well established in the solution phase into the solid state, which can enable a broad range of practical applications, such as high-efficiency molecular separation, heterogeneous catalysis, and pollution remediation. However, it is still a challenging task to construct macrocycle-embedded COFs. In this work, a novel pillar[5]arene-derived (P5) hetero-porous COF, denoted as P5-COF, was rationally designed and synthesized. Featuring the unique backbone structure, P5-COF exhibited selective adsorption of C2H2 over C2H4 and C2H6, as well as significantly enhanced host-guest binding interaction with paraquat, in comparison with the pillar[5]arene-free COF analog, Model-COF. The present work established a new strategy for developing COFs with customizable molecular recognition/separation properties through the bottom-up "pre-porous macrocycle to porous framework" design.
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