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Redox Non‐Innocence of Nitrosobenzene at Nickel
Authors:Dr Subrata Kundu  Prof?Dr S Chantal E Stieber  Dr Maryline G Ferrier  Dr Stosh A Kozimor  Dr Jeffery A Bertke  Prof?Dr Timothy H Warren
Institution:1. Department of Chemistry, Georgetown University, Washington, DC, USA;2. Inorganic, Isotope and Actinide Chemistry, Los, Alamos National Laboratory, Los Alamos, NM, USA;3. Department of Chemistry and Biochemistry, California State Polytechnic University, Pomona, CA, USA
Abstract:Nitrosobenzene (PhNO) serves as a stable analogue of nitroxyl (HNO), a biologically relevant, redox‐active nitric oxide derivative. Capture of nitrosobenzene at the electron‐deficient β‐diketiminato nickel(I) complex iPr2NNF6]Ni results in reduction of the PhNO ligand to a (PhNO)./? species coordinated to a square planar NiII center in iPr2NNF6]Ni(η2‐ONPh). Ligand centered reduction leads to the (PhNO)2? moiety bound to NiII supported by XAS studies. Systematic investigation of structure–reactivity patterns of (PhNO)./? and (PhNO)2? ligands reveals parallels with superoxo (O2)./? and peroxo (O2)2? ligands, respectively, and forecasts reactivity patterns of the more transient HNO ligand.
Keywords:nickel  nitric oxide  nitrosobenzene  redox-active ligands  X-ray spectroscopy
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