Difluorocarbene Generation via a Spin-Forbidden Excitation under Visible Light Irradiation

The generation of difluorocarbene from difluoromethane bis(sulfonium ylide) <b>1</b> through spin-forbidden excitation under irradiation with 450 nm blue light was reported. The formation of difluorocarbene was confirmed by its reaction with styrene derivatives for the generation of difluorocyclopropanation and insertion into RX-H bonds (X = O, S) for the generation of RXCF<sub>2</sub>H. The spin-forbidden excitation mechanism for the formation of difluorocarbene from difluoromethane bis(sulfonium ylide) was supported by spectroscopic and kinetic studies as well as computational chemistry. The homolytic cleavage of two S-C bonds in compound <b>1</b> under irradiation was confirmed by time-resolved EPR spectroscopic studies of the precursor's free-radical-capturing reaction, as well as the isolation of the dimer of dimethyl (phenylthiol)malonyl radical. Further studies showed that the homolytic cleavage process occurred asynchronously in the solvent cage based on the isotope-labeled scrambling experiments and DFT calculations.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-11-04
DOI
https://doi.org/10.1021/jacs.4c10939
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.62

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article

Difluorocarbene Generation via a Spin-Forbidden Excitation under Visible Light Irradiation

Tianfei Liu, Ganglong Cui, Yijing Ling, Guang‐Ning Pan et al.
3 citations
Journal of the American Chemical Society
Fluorine in Organic Chemistry
0.62
article

Difluorocarbene Generation via a Spin-Forbidden Excitation under Visible Light Irradiation

Tianfei Liu, Ganglong Cui, Yijing Ling, Guang‐Ning Pan, Shan Liu, Feng Gao, Yin Yang, Qilong Shen
article en
3 citations

Abstract

The generation of difluorocarbene from difluoromethane bis(sulfonium ylide) <b>1</b> through spin-forbidden excitation under irradiation with 450 nm blue light was reported. The formation of difluorocarbene was confirmed by its reaction with styrene derivatives for the generation of difluorocyclopropanation and insertion into RX-H bonds (X = O, S) for the generation of RXCF<sub>2</sub>H. The spin-forbidden excitation mechanism for the formation of difluorocarbene from difluoromethane bis(sulfonium ylide) was supported by spectroscopic and kinetic studies as well as computational chemistry. The homolytic cleavage of two S-C bonds in compound <b>1</b> under irradiation was confirmed by time-resolved EPR spectroscopic studies of the precursor's free-radical-capturing reaction, as well as the isolation of the dimer of dimethyl (phenylthiol)malonyl radical. Further studies showed that the homolytic cleavage process occurred asynchronously in the solvent cage based on the isotope-labeled scrambling experiments and DFT calculations.

Journal of the American Chemical SocietyVol. 146(45)
Chinese Academy of Sciences (CN), Nankai University (CN), Beijing Normal University (CN), Shanghai Institute of Organic Chemistry (CN), Unité Matériaux et Transformations (FR)
National Natural Science Foundation of China, Chinese Academy of Sciences, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 35%
Fluorine in Organic Chemistry
0.62
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Difluorocarbene Generation via a Spin-Forbidden Excitation under Visible Light Irradiation — Tianfei Liu, Ganglong Cui, et al. · Journal of the American Chemical Society (2024) | TGRS Research Map | TGRS