Issue 8, 1998

Structure of lithium–p-semiquinonates in non-aqueous solution *

Abstract

The reaction of phenyllithium with p-quinones (1,4-benzoquinone, 2,6-di-tert-butyl-1,4-benzoquinone, 1,4-naphthoquinone) in tetrahydrofuran gave the phenyl radical, which goes to biphenyl, and the corresponding lithium semiquinonate. The latter can also be obtained by direct reaction between lithium and the p-quinone. Electron spin resonance spectroscopy showed that a solution of the lithium derivative contains both monomeric and dimeric species. Adducts with 4-methylpyridine have also been prepared. Quantum-mechanical calculations were consistent with the ESR results. Related experiments with potassium derivatives were also performed.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1998, 1371-1376

Structure of lithium–p-semiquinonates in non-aqueous solution *

M. A. Brown, B. R. McGarvey and D. G. Tuck, J. Chem. Soc., Dalton Trans., 1998, 1371 DOI: 10.1039/A800033F

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