Infrared Spectroscopic Study of Perfluorobenzyl Peroxyl Radical and Its UV Photolysis Products in An Argon Matrix

The perfluorobenzyl peroxyl radical (C<sub>6</sub>F<sub>5</sub>CF<sub>2</sub>O<sub>2</sub>) was prepared by the reaction of the perfluorobenzyl radical, generated in the gas phase by vacuum pyrolysis of the perfluorobenzyl iodide, with molecular oxygen. The IR spectra of the radicals C<sub>6</sub>F<sub>5</sub>CF<sub>2</sub>O<sub>2</sub> and C<sub>6</sub>F<sub>5</sub>CF<sub>2</sub><sup>18</sup>O<sub>2</sub> trapped in argon matrices at 10 K were measured for the first time and assigned to two conformers with the O-O moiety in anti- and gauche orientation with respect to the C-C bond by comparing the results of the matrix isolation IR spectroscopy study with the data of quantum chemical calculations at the B3LYP/aug-cc-pVTZ and CBS-QB3 levels of theory. UV photolysis of this peroxyl radical resulted in the elimination of F<sub>2</sub>C═O with the formation of the perfluorophenoxyl radical C<sub>6</sub>F<sub>5</sub>O, which formed complexes in the matrix. This reaction pathway considerably differs from that observed for the unsubstituted benzyl peroxyl radical, which decomposes to hydroxyl radical and benzaldehyde.

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Journal
The Journal of Physical Chemistry A
Published
2025-07-21
DOI
https://doi.org/10.1021/acs.jpca.5c02095
Primary Topic
Photochemistry and Electron Transfer Studies
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article
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article

Infrared Spectroscopic Study of Perfluorobenzyl Peroxyl Radical and Its UV Photolysis Products in An Argon Matrix

E. G. Baskir, V. D. Gvozdev
The Journal of Physical Chemistry A
Photochemistry and Electron Transfer Studies
article

Infrared Spectroscopic Study of Perfluorobenzyl Peroxyl Radical and Its UV Photolysis Products in An Argon Matrix

E. G. Baskir, V. D. Gvozdev
article en

Abstract

The perfluorobenzyl peroxyl radical (C<sub>6</sub>F<sub>5</sub>CF<sub>2</sub>O<sub>2</sub>) was prepared by the reaction of the perfluorobenzyl radical, generated in the gas phase by vacuum pyrolysis of the perfluorobenzyl iodide, with molecular oxygen. The IR spectra of the radicals C<sub>6</sub>F<sub>5</sub>CF<sub>2</sub>O<sub>2</sub> and C<sub>6</sub>F<sub>5</sub>CF<sub>2</sub><sup>18</sup>O<sub>2</sub> trapped in argon matrices at 10 K were measured for the first time and assigned to two conformers with the O-O moiety in anti- and gauche orientation with respect to the C-C bond by comparing the results of the matrix isolation IR spectroscopy study with the data of quantum chemical calculations at the B3LYP/aug-cc-pVTZ and CBS-QB3 levels of theory. UV photolysis of this peroxyl radical resulted in the elimination of F<sub>2</sub>C═O with the formation of the perfluorophenoxyl radical C<sub>6</sub>F<sub>5</sub>O, which formed complexes in the matrix. This reaction pathway considerably differs from that observed for the unsubstituted benzyl peroxyl radical, which decomposes to hydroxyl radical and benzaldehyde.

The Journal of Physical Chemistry AVol. 129(30)
N.D. Zelinsky Institute of Organic Chemistry (RU)
Openalex Percentile: Top 83%
Photochemistry and Electron Transfer Studies
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Infrared Spectroscopic Study of Perfluorobenzyl Peroxyl Radical and Its UV Photolysis Products in An Argon Matrix — E. G. Baskir, V. D. Gvozdev · The Journal of Physical Chemistry A (2025) | TGRS Research Map | TGRS