EDA Complexation of Two Donor Molecules Initiating Radical Cation Cyclizations

Abstract In this study, a catalyst-free EDA complexation of two donor molecules using an acidic solvent is presented. The electron-rich aromatic compound (E)-anethole is slowly protonated by the solvent hexafluoroisopropanol (HFIP), leading to the rapid formation of a photoactive EDA complex between a protonated (E)-anethole and another (E)-anethole molecule. This resulting EDA complex initiates radical chain cyclization reactions under green light irradiation.

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Publication Details

Journal
Synthesis
Published
2025-01-16
DOI
https://doi.org/10.1055/a-2518-0987
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

EDA Complexation of Two Donor Molecules Initiating Radical Cation Cyclizations

Rubaishan Jeyaseelan, Julian C. G. Kürschner, Lena Lezius, Martin Utikal et al.
Synthesis
Radical Photochemical Reactions
article

EDA Complexation of Two Donor Molecules Initiating Radical Cation Cyclizations

Rubaishan Jeyaseelan, Julian C. G. Kürschner, Lena Lezius, Martin Utikal, Line Næsborg
article en

Abstract

Abstract In this study, a catalyst-free EDA complexation of two donor molecules using an acidic solvent is presented. The electron-rich aromatic compound (E)-anethole is slowly protonated by the solvent hexafluoroisopropanol (HFIP), leading to the rapid formation of a photoactive EDA complex between a protonated (E)-anethole and another (E)-anethole molecule. This resulting EDA complex initiates radical chain cyclization reactions under green light irradiation.

SynthesisVol. 57(13)
University of Münster (DE)
Fonds der Chemischen Industrie, Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 99%
Radical Photochemical Reactions
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