Abstract

Potassium and tin(II) derivatives of the paramagnetic forms of the redox-active 2,6-bis(2,6-diisopropylphenyliminomethyl)pyridine were synthesized and studied by means of EPR spectroscopy. It was shown that the reaction with metallic potassium involves the three-electron step reduction of the organic ligand to form a radical anion, dianion, and trianion radical, respectively. The reactions of the tin(II) diiminopyridine derivatives with metallic magnesium give complexes comprising the radical anion form of the ligand and a low-valence metal center. The geometries of the paramagnetic products and their spin density distributions were explored in terms of the density functional theory.

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