Cis-Trans and Length-Selective Molecular Discrimination of Halogenated Organic Compounds by a Crystalline Hybrid Macrocyclic Arene.

Abstract

The development of adsorbents with robust molecular discrimination capabilities for halogenated organic compounds (HOCs) holds significant importance due to their potential in adsorptive separation and mitigation of associated health risks. In this study, we report a molecular discrimination behavior based on crystalline hybrid macrocyclic arene H, offering precise capture of cis-trans isomers and length-selective separation of HOCs. The activated H crystals (Hα) demonstrate exceptional discrimination and separation performance by selectively capturing trans-1,2-dichloroethylene (trans-DCE) from cis/trans-isomer mixtures with a high selectivity of 98.8%. Evidenced by single-crystal X-ray diffraction and density functional theory (DFT) calculations, this high adsorption selectivity arises from the formation of more stable complex crystals between H and the preferred guest trans-DCE. Moreover, Hα exhibits the ability to selectively trap size-matched 1,2-dibromoethane (DBE) from mixtures of alkylene dibromides with varying alkane-chain lengths, although their capture and separation are recognized to be difficult as a consequence of low-polarity bonds. The solid-state transformations between guest-free and guest-containing Hα crystals indicate their recyclability, showcasing promising prospects for potential applications.