Mechanism of F <sup>+</sup> Salts Catalyzed Aziridine Synthesis: F‐Halogen Bonding Catalysis or F‐Cation Transfer Catalysis? <sup>†</sup>

Comprehensive Summary Whether the fluorine atom (F) can engage in a halogen bond (XB) has remained a subject of ongoing debate. The discovery of N ‐fluoropyridinium triflate as a unique "F‐cation organocatalyst" for aziridine synthesis has generally been considered the first instance of F‐halogen bonding catalysis. Nevertheless, the mechanistic details of this reaction have remained elusive, and compelling evidence supporting the F‐halogen bond catalysis has been lacking. In this study, we present an in‐depth computational investigation of the mechanism of this reaction to gain insights into the intriguing role of the F‐cation organocatalyst. Our results, however, are inconsistent with the previous prevalent F‐halogen bonding catalysis mechanism but instead, bring to light a new fluorine cation transfer mechanism. This novel mechanism is supported by control experiments and can explain the observed cis ‐ trans selectivity.

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2025-09-18
DOI
https://doi.org/10.1002/cjoc.70270
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Mechanism of F + Salts Catalyzed Aziridine Synthesis: F‐Halogen Bonding Catalysis or F‐Cation Transfer Catalysis? †

Sean P. Bew, Xiao‐Song Xue, Hao‐Dong Tan, Cai Liu
Chinese Journal of Chemistry
Synthesis and Catalytic Reactions
article

Mechanism of F + Salts Catalyzed Aziridine Synthesis: F‐Halogen Bonding Catalysis or F‐Cation Transfer Catalysis? †

Sean P. Bew, Xiao‐Song Xue, Hao‐Dong Tan, Cai Liu
article en

Abstract

Comprehensive Summary Whether the fluorine atom (F) can engage in a halogen bond (XB) has remained a subject of ongoing debate. The discovery of N ‐fluoropyridinium triflate as a unique "F‐cation organocatalyst" for aziridine synthesis has generally been considered the first instance of F‐halogen bonding catalysis. Nevertheless, the mechanistic details of this reaction have remained elusive, and compelling evidence supporting the F‐halogen bond catalysis has been lacking. In this study, we present an in‐depth computational investigation of the mechanism of this reaction to gain insights into the intriguing role of the F‐cation organocatalyst. Our results, however, are inconsistent with the previous prevalent F‐halogen bonding catalysis mechanism but instead, bring to light a new fluorine cation transfer mechanism. This novel mechanism is supported by control experiments and can explain the observed cis ‐ trans selectivity.

Chinese Journal of ChemistryVol. 43(24)
University of East Anglia (GB), Shanghai Institute of Organic Chemistry (CN), ZheJiang Academy of Agricultural Sciences (CN)
Openalex Percentile: Top 81%
Synthesis and Catalytic Reactions
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