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.

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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

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article

Tetrafluororesorcin[4]arene Hexameric Capsule Enables the Expansion of the Reactivity Space in Supramolecular Catalysis

Konrad Tiefenbacher, Chintu Das, Tian‐Ren Li, GiovanniMaria Piccini
8 citations
Journal of the American Chemical Society
Supramolecular Chemistry and Complexes
7.49
article

Tetrafluororesorcin[4]arene Hexameric Capsule Enables the Expansion of the Reactivity Space in Supramolecular Catalysis

Konrad Tiefenbacher, Chintu Das, Tian‐Ren Li, GiovanniMaria Piccini
article en
8 citations

Abstract

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.

Journal of the American Chemical SocietyVol. 147(13)
University of Modena and Reggio Emilia (IT), University of Basel (CH), ETH Zurich (CH), RWTH Aachen University (DE)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Openalex Percentile: Top 3%
Supramolecular Chemistry and Complexes
7.49
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