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Selective CO2 Adsorption in a Supramolecular Organic Framework

机译:超分子有机骨架中的选择性CO2吸附

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摘要

Considering the rapidly rising CO2 level, there is a constant need for versatile materials which can selectively adsorb CO2 at low cost. The quest for efficient sorptive materials is still on since the practical applications of conventional porous materials possess certain limitations. In that context, we designed, synthesized, and characterized two novel supramolecular organic frameworks based on C-pentylpyrogallol[4]arene (PgC(5)) with spacer molecules, such as 4,4-bipyridine (bpy). Highly optimized and symmetric intermolecular hydrogen-bonding interactions between the main building blocks and comparatively weak van der Waals interactions between solvent molecules and PgC(5) leads to the formation of robust extended frameworks, which withstand solvent evacuation from the crystal lattice. The evacuated framework shows excellent affinity for carbon dioxide over nitrogen and adsorbs ca. 3wt % of CO2 at ambient temperature and pressure.
机译:考虑到迅速升高的CO 2水平,一直需要能够以低成本选择性吸附CO 2的通用材料。由于常规多孔材料的实际应用具有一定的局限性,因此仍然需要有效的吸附材料。在这种情况下,我们设计,合成和表征了基于C-戊基邻苯三酚[4]芳烃(PgC(5))的新型超分子有机骨架,该骨架具有间隔分子,例如4,4-联吡啶(bpy)。主要构件之间的高度优化和对称的分子间氢键相互作用以及溶剂分子与PgC之间的较弱的范德华相互作用(5)导致形成坚固的扩展骨架,可承受溶剂从晶格中逸出。抽空的框架对二氧化碳显示出对氮的优异亲和力,并吸收约。在环境温度和压力下3wt%的CO2。

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