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Fine-tuning the N-donor ability of a bidentate aminopyridyl ligand facilitated the selective synthesis of complexes 1 (no methyl substituent) and 2 (with a methyl substituent) which possess valence tautomeric nickel(II) semiquinonato and nickel(III) catecholato frameworks, respectively.
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Ohtsu et al. (2004) studied this question.
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