Selective Separation of Hexachloroplatinate(IV) Dianions Based on Exo‐Binding with Cucurbit[6]uril

Abstract

The recognition and separation of anions attracts attention from chemists, materials scientists, and engineers. Employing exo-binding of artificial macrocycles to selectively recognize anions remains a challenge in supramolecular chemistry. We report the instantaneous co-crystallization and concomitant co-precipitation between [PtCl₆ ]^2- dianions and cucurbit[6]uril, which relies on the selective recognition of these dianions through noncovalent bonding interactions on the outer surface of cucurbit[6]uril. The selective [PtCl₆ ]^2- dianion recognition is driven by weak [Pt-Cl⋅⋅⋅H-C] hydrogen bonding and [Pt-Cl⋅⋅⋅C=O] ion-dipole interactions. The synthetic protocol is highly selective. Recognition is not observed in combinations between cucurbit[6]uril and six other Pt- and Pd- or Rh-based chloride anions. We also demonstrated that cucurbit[6]uril is able to separate selectively [PtCl₆ ]^2- dianions from a mixture of [PtCl₆ ]^2- , [PdCl₄ ]^2- , and [RhCl₆ ]^3- anions. This protocol could be exploited to recover platinum from spent vehicular three-way catalytic converters and other platinum-bearing metal waste.