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Nitroxide chemistry. Part XII. Free radical formation in the reactions between trifluoronitrosomethane and some 1,3-diketones
Journal of the Chemical Society Perkin Transactions 21977Iss. 1, pp. 7–7
Abstract
The 1,3-diketones RCO·CH2·COR′(R = R′= CH3 or CF3, and R = CH3, R′= CF3) react with trifluoronitrosomethane to generate the nitroxide radicals CF3·N(Ȯ)·CH(COR′)·COR and their tautomers CF3N(Ȯ)·C(COR′):C(OH)R together with the iminoxy-radicals (RCO)(R′CO)C:N·O, all detected by e.s.r. spectroscopy. Diethyl 2-methyl-3-oxosuccinate affords only the radical CF3·N(Ȯ)·CMe(CO2Et)CO·CO2Et under similar conditions. Intermediate hydroxylamine anions CF3·N(Ō)·CH(COR)·COR′, are proposed as intermediates which can undergo further reaction by two different pathways to give the observed radicals. The e.s.r. parameters of the various nitroxide radicals are given, and these are interpreted in terms of a deviation from planarity at the nitrogen atom.
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