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Radical cations of 1,4-dialkoxybenzenes and alkyl 1,4-dialkoxybenzenes generated through one-electron oxidation by perfluorodiacyl peroxides

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Radical cations of 1,4-dialkoxybenzenes 1 and 2 and alkyl 1,4-dialkoxybenzenes 3–9 generated in oxidation of the parent donors by perfluorodi[1-(2-fluorosulfonyl)ethoxy]propionyl peroxide 10 at −40°C and pentafluorobenzoyl peroxide 11 at 15°C were observed by ESR. Radical cation 6, generated in other oxidation systems, i.e., Ce(SO4)2/THF, NH4/OAc and (NH4)2S2O8/HOAc, has also been investigated. Based on ESR observation and products analysis, an electron-transfer mechanism of the oxidation reaction is proposed and the influencing factors on hyperfine splitting constants of the radical cations are discussed.

10.1163/156856706775372762
/content/journals/10.1163/156856706775372762
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/content/journals/10.1163/156856706775372762
2006-02-01
2016-12-10

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