Volume 29, Issue 11 e202203588
Research Article

Gated, Selective Anion Exchange in Functionalized Self-Assembled Cage Complexes

Bryce da Camara

Bryce da Camara

Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA, 92521 USA

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Noa Bar Ziv

Noa Bar Ziv

Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA, 92521 USA

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Veronica Carta

Veronica Carta

Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA, 92521 USA

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Gabriela A. Mota Orozco

Gabriela A. Mota Orozco

Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA, 92521 USA

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Hoi-Ting Wu

Hoi-Ting Wu

Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA, 92521 USA

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Prof. Ryan R. Julian

Prof. Ryan R. Julian

Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA, 92521 USA

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Prof. Richard J. Hooley

Corresponding Author

Prof. Richard J. Hooley

Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA, 92521 USA

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First published: 21 November 2022
Citations: 3

Graphical Abstract

Appending functional groups to the exterior of Zn4L4 self-assembled cages allows gated control of anion binding. The external groups act as a “doorstop”, preventing ligand rotation and slowing the guest exchange rate. Bulky groups affect both anion egress and ingress, introducing an extra layer of selectivity to the exchange. Small changes can have large effects: affinities for anions as similar as PF6 and SbF6 can vary by as much as 400-fold between identically sized cavities.

Abstract

Appending functional groups to the exterior of Zn4L4 self-assembled cages allows gated control of anion binding. While the unfunctionalized cages contain aryl groups in the ligand that can freely rotate, attaching inert functional groups creates a “doorstop”, preventing rotation and slowing the guest exchange rate, even though the interiors of the host cavities are identically structured. The effects on anion exchange are subtle and depend on multiple factors, including anion size, the nature of the leaving anion, and the electron-withdrawing ability and steric bulk of the pendant groups. Multiple exchange mechanisms occur, and the nature of the external groups controls associative and dissociative exchange processes: these bulky groups affect both anion egress and ingress, introducing an extra layer of selectivity to the exchange. Small changes can have large effects: affinities for anions as similar as PF6 and SbF6 can vary by as much as 400-fold between identically sized cavities.

Conflict of interest

The authors declare no conflict of interest.

Data Availability Statement

The data that support the findings of this study are available in the Supporting material of this article. Deposition Number 2213841 (for Fe-4 ⋅ SbF6) contains the supplementary crystallographic data for this paper. These data are provided free of charge by the joint Cambridge Crystallographic Data Centre and Fachinformationszentrum Karlsruhe Access Structures service.