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Nitric Oxide Release from a Nickel Nitrosyl Complex Induced by One-Electron Oxidation

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posted on 19.02.2016 by Ashley M. Wright, Homaira T. Zaman, Guang Wu, Trevor W. Hayton
Reaction of [Ni­(NO)­(bipy)]­[PF6] (2) with AgPF6 or [NO]­[PF6] in MeCN results in formation of [Ni­(bipy)x(MeCN)y]2+ and release of NO gas in moderate yields. In contrast, the addition of the inner sphere oxidant Ph2S2 to 2 does not result in denitrosylation. Instead, the diphenyldisulfide adduct [{(bipy)­(NO)­Ni}2(μ-S2Ph2)]­[PF6]2 (3) is formed in good yield. However, oxidation of 2 with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) does results in cleavage of the Ni–NO bond and generation of NO. The metal-containing product, [(bipy)­Ni­(η2-TEMPO)]­[PF6] (4), can be isolated as an orange-brown solid in excellent yields. In the solid state, complex 4 contains a side-on bound TEMPO ligand, which is characterized by a long N–O bond length [1.383(2) Å]. The contrasting reactivity of Ph2S2 and TEMPO likely relates to their different redox potentials, as Ph2S2 is a relatively weak oxidant. Finally, the addition of pyridine-N-oxide to 2 results in the formation of the adduct, [(bipy)­Ni­(NO)­(ONC5H5)]­[PF6] (5). No evidence of NO release is observed in this reaction, probably because of the low one-electron (1e) reduction potential of pyridine-N-oxide.