Liu Lu, Hu Yiming, Huang Shaofeng, Jin Yinghua, Cui Jingnan, Gong Weitao, Zhang Wei
State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology Dalian 116024 P. R. China
Department of Chemistry, University of Colorado Boulder Boulder Colorado 80309 USA
Chem Sci. 2021 Sep 15;12(40):13316-13320. doi: 10.1039/d1sc03680g. eCollection 2021 Oct 20.
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 (, 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 () hetero-porous COF, denoted as , was rationally designed and synthesized. Featuring the unique backbone structure, exhibited selective adsorption of CH over CH and CH, as well as significantly enhanced host-guest binding interaction with paraquat, in comparison with the pillar[5]arene-free COF analog, . 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.
在固态下保持大环穴状配体的永久性可及孔道和选择性分子识别能力是非常理想的。将定义明确的离散大环主体整合到有序多孔聚合物框架(即共价有机框架,COFs)中,是一种很有前景的策略,可将许多在溶液相中已确立的超分子化学概念和原理转化到固态中,这能够实现广泛的实际应用,如高效分子分离、多相催化和污染修复。然而,构建嵌入大环的COFs仍然是一项具有挑战性的任务。在这项工作中,合理设计并合成了一种新型的基于柱[5]芳烃的()杂多孔COF,记为。与不含柱[5]芳烃的COF类似物相比,具有独特的主链结构,对CH4表现出对C2H4和C2H6的选择性吸附,以及与百草枯显著增强的主客体结合相互作用。本工作通过自下而上的“预多孔大环到多孔框架”设计,建立了一种开发具有可定制分子识别/分离性能的COFs的新策略。