Issue 21, 1998

The interaction of indium(III) iodide species with substituted ortho- and para-quinones

Abstract

The interactions of substituted ortho- and para-quinones with indium(III) halides and the InI4 anion have been studied in non-aqueous solution. para-Quinones and InI3 give rise to stable 1∶1 adducts, which are diamagnetic in the solid state, but which decompose in solution to form ( p-sq)InI2 derivatives, where p-sq˙– is the corresponding semiquinonate. With ortho-quinones, the reaction products are (o-sq)InI2 which react with 4-methylpyridine (pic) to form (o-sq)InI2pic2. The electron spin resonance spectra of these products, and their solution chemistry, are discussed. The reactions involve intramolecular one-electron transfer, resulting in oxidation of the iodide ligand. In contrast, the reaction of 3,5-di-tert-butyl-1,2-benzoquinone with InI4 apparently involves intermolecular electron transfer; in this case, the products are I3 and the corresponding catecholate (dbc), isolated as the solid InI(dbc)pic2. The mechanisms of these various processes are discussed.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1998, 3543-3548

The interaction of indium(III) iodide species with substituted ortho- and para-quinones

M. A. Brown, B. R. McGarvey and D. G. Tuck, J. Chem. Soc., Dalton Trans., 1998, 3543 DOI: 10.1039/A804124E

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