A Water‐Stable Ionic MOF for the Selective Capture of Toxic Oxoanions of Se^VI and As^V and Crystallographic Insight into the Ion‐Exchange Mechanism

Abstract

Selectively capturing toxic oxoanions of selenium and arsenic is highly desired for the remediation of hazardous waste. Ionic metal-organic frameworks (iMOFs) especially cationic MOFs (iMOF-C) as ion-exchange materials, featuring aqueous phase stability, present a robust pathway for sequestration of the oxoanions owing to their ability to prevent leaching because of their ionic nature. On account of scarcity of water-stable cationic MOFs, the capture of oxoanions of selenium and arsenic has been a major challenge and has not been investigated using iMOFs. Herein, we demonstrate large scale synthesis of cationic MOF, viz. iMOF-1C that exhibits selective capture of oxoanions of Se^VI (SeO₄^2- ) and As^V (HAsO₄^2- ) in water with a maximum sorption capacity of 100 and 85 mg g^-1 , respectively. This represents among the highest uptake capacities observed for selenate oxoanion in MOFs. Further, the ion-exchange mechanism was directly unveiled by single crystal analysis, which revealed variable modes of host-guest binding.