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1 January 2006 A TRIR, TREPR and Computational Study on the Reactivity and Structure of the 2,2,2-Trifluoroethoxycarbonyl Radical
Christoph Kolano, Götz Bucher, Dirk Grote, Olaf Schade, Wolfram Sander
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Abstract

The 2,2,2-trifluoroethoxycarbonyl radical, 3b, has been generated by pulsed irradiation of 9-fluorenone oxime 2,2,2-trifluoroethyl oxalate 1b in carbon tetrachloride and acetonitrile solution. It was characterized by time-resolved electron paramagnetic resonance spectroscopy (EPR) and infrared spectroscopy. The radical has a lifetime in the range of microseconds and can be detected within the rise time of our time-resolved equipment before undergoing recombination or reactions with the solvent. No decarbonylation or decarboxylation was observed. In the presence of oxygen, the radical is quenched to yield the 2,2,2-trifluoroethoxycarbonylperoxy radical 4b, which has again a lifetime in the range of several microseconds. Time-resolved electron paramagnetic resonance spectroscopy (TREPR) allowed for the detection of a 1 : 1 : 1 triplet of the fluorene-9-iminyl radical 7 at g = 2.0032 and a 1 : 3 : 3 : 1 quartet with additional hyperfine splitting (HFS) due to proton coupling at g = 2.001 for the trifluoroethoxycarbonyl radical 3b. Calculations indicate that alkoxycarbonyl radicals can exist in conformations that are s-trans or s-cis with respect to the R-O-C(O)·dihedral. A comparison of experimental TREPR spectra with simulations indicates that the s-trans conformer is observed in the case of the ethoxycarbonyl radical, 3a. In the case of the trifluorethoxycarbonyl radical, 3b, however, the additional proton HFS observed shows that it is the s-cis conformer that is formed. As calculations give evidence for a fairly high activation enthalpy for s-cis-s-trans interconversion of alkoxycarbonyl radicals, this discrepancy is likely due to differing conformational preferences of the precursor molecules.

Christoph Kolano, Götz Bucher, Dirk Grote, Olaf Schade, and Wolfram Sander "A TRIR, TREPR and Computational Study on the Reactivity and Structure of the 2,2,2-Trifluoroethoxycarbonyl Radical," Photochemistry and Photobiology 82(1), 332-338, (1 January 2006). https://doi.org/10.1562/2005-05-30-RA-554
Received: 30 May 2005; Accepted: 28 September 2005; Published: 1 January 2006
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