期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 14, 期 1, 页码 206-210出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ob02210j
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资金
- Deutsche Forschungsgemeinschaft (DFG)
A simple and practical method for the determination of rate constants for trifluoromethyl radical addition to various alkenes by applying competition kinetics is introduced. In the kinetic experiments the trifluoromethyl radicals are generated in situ from a commercially available hypervalent-iodine-CF3 reagent (Togni-reagent) by SET-reduction with TEMPONa in the presence of TEMPO and a pi-acceptor. From the relative ratio of TEMPOCF3 and CF3-addition product formed, which is readily determined by F-19-NMR spectroscopy, rate constants for trifluoromethyl radical addition to the pi-acceptor can be calculated. The practical method is also applicable to measure rate constants for the addition of other perfluoroalkyl radicals to alkenes as documented for CF3CF2-radical addition reactions.
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