Influence of nitro substituents on the redox, electronic, and proton reduction catalytic behavior of phenolate-based [N

We report on the synthesis, redox, electronic, and catalytic behavior of two new cobalt(iii) complexes, namely [CoIII(L1)MeOH] (1) and [CoIII(L2)MeOH] (2). These species contain nitro-rich, phenolate-based pentadentate ligands and present dramatically distinct properties associated with the position in which the -NO2 substituents are installed. Species 1 displays nitro-substituted phenolates, and exhibits irreversible redox response and negligible catalytic activity, whereas 2 has fuctionalized phenylene moieties, shows much improved redox reversibility and catalytic proton reduction activity at low overpotentials. A concerted experimental and theoretical approach sheds some light on these drastic differences.