Abstract
Radical cations generated during electrochemical oxidation of a series of trivalent phosphorus compounds, alone or in the presence of 3,3-dimethyl-2-t-butylbut-1-ene, have been studied using e.s.r. spectroscopy. The oxidations were carried out in nitrile or dichloromethane solvents and the cell containing the working electrode was situated in the cavity of the spectrometer. Oxidation of X3P alone gives rise to the spectrum of the phosphine dimer cation radical, (X3PPX3)+, produced by rapid reaction of the initially formed phosphinium radical cation, X3P+, with a further molecule of phosphine. Trialkyl phosphites did not give detectable concentrations of dimer cation radicals in nitrile solvents, probably because of preferential reaction of (RO)3P+ with the solvent. In the presence of 3,3-dimethyl-2-t-butylbut-1-ene the spectra of the dimer cation radicals were completely or partially quenched and replaced by those of the adducts But2ĊCH2PX3. The phosphorus hyperfine splittings of both (X3PPX3)+ and But2ĊCH2PX3 increased with the electronegativity of the ligands X, and these trends are interpreted in terms of changes in hybridisation at phosphorus.
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Schedule a callMore From: Journal of the Chemical Society, Perkin Transactions 2
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