Abstract
A reaction of tin(IV) bis-o-amidophenolate complex based on redox-active 4,6-di-tert-butyl-N-(2,6-diisopropylphenyl)-o-aminophenol with various allyl halides was studied. This process includes the addition of 1 equiv. of allyl halide to the starting complex and is accompanied by the change in the redox state of one of the redox-active ligands. The reaction results in the formation of a new carbon—carbon bond between the allylic fragment and the carbon atom at position 5 of the ligand o-iminoquinone ring, as well as a tin—halogen bond. The structure and composition of compounds synthesized were confirmed by ESR, NMR, and IR spectroscopy and elemental analysis.
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