Anion‐Controlled Structural Interconversion of Palladium Cages Enables Separations by Selective Guest Capture and Release
Self-assembled host-guest systems provide a powerful platform for molecular recognition and binding. Achieving the controlled and selective release of bound guests remains challenging, typically relying on destructive stimuli. Herein, we report that asymmetric ligand L assembles to form an interconverting pair of palladium(II)-based metal-organic cages, Pd<sub>4</sub>L<sub>8</sub>(BF<sub>4</sub>)<sub>8</sub> and Pd<sub>6</sub>L<sub>12</sub>(NTf<sub>2</sub>)<sub>12</sub>, capable of undergoing clean, reversible, and quantitative structural interconversion triggered by specific counter-anions. The two cages exhibit distinct guest recognition profiles, with each cage binding a different subset of guests. We use anion-mediated structural transformations to achieve orthogonal, multi-cycle, selective binding and release of different guest molecules under mild conditions. To showcase the power of this supramolecular catch-and-release purification, we designed and validated a closed-loop purification process, successfully isolating Darunavir from a complex mixture of pharmaceutical molecules with exceptional selectivity and efficiency. This work highlights a broadly applicable strategy for advanced molecular separations and selective pharmaceutical purification.
Authors
- Charlie T. McTernan (ORCID: https://orcid.org/0000-0003-1359-0663)
- Zhe Li
- Tanya K Ronson
Institutions
- King's College - North Carolina (US)
- King's College London (GB)
- University of Cambridge (GB)
- The Francis Crick Institute (GB)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2026-03-05
- DOI
- https://doi.org/10.1002/anie.202525696
- Primary Topic
- Supramolecular Chemistry and Complexes
- Type
- article
- Field-Weighted Citation Impact
- 0.00