Tetrafluororesorcin[4]arene Hexameric Capsule Enables the Expansion of the Reactivity Space in Supramolecular Catalysis
This study presents the development and catalytic applications of the tetrafluororesorcin[4]arene hexameric capsule (capsule II) as a novel supramolecular catalyst. It demonstrates unprecedented catalytic activity, enabling the β-selective glycosylation of glycals to 2-deoxy glycosides─a transformation that has not been achieved before in molecular and supramolecular catalysis. Mechanistic investigations, including experimental and computational studies, revealed that the high β-selectivity arises from a proton wire mechanism along the capsule's surface, coupling glycal protonation with nucleophile deprotonation. Control experiments confirmed the unique reactivity of capsule II compared to its nonfluorinated predecessor, capsule I, showcasing its potential to expand the boundaries of supramolecular catalysis.
Authors
- Konrad Tiefenbacher (ORCID: https://orcid.org/0000-0002-3351-6121)
- Chintu Das
- Tian‐Ren Li (ORCID: https://orcid.org/0000-0003-1468-4565)
- GiovanniMaria Piccini (ORCID: https://orcid.org/0000-0002-3511-4281)
Institutions
- University of Modena and Reggio Emilia (IT)
- University of Basel (CH)
- ETH Zurich (CH)
- RWTH Aachen University (DE)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-02-05
- DOI
- https://doi.org/10.1021/jacs.4c17029
- Citations
- 8
- Primary Topic
- Supramolecular Chemistry and Complexes
- Type
- article
- Field-Weighted Citation Impact
- 7.49
Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung