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Structural characterization of a hydroperoxo nickel complex and its autoxidation: mechanism of interconversion between peroxo, superoxo, and hydroperoxo species

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Pincer-stabilized nickel(I) complexes readily react with molecular oxygen to form dinuclear 1,2-μ-peroxo-bridged nickel(II) complexes, which are the major components of a dynamic equilibrium with the corresponding mononuclear superoxo species. The peroxo complexes further react with hydrogen peroxid...

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Bibliographic Details
Main Authors: Rettenmeier, Christoph Alexander (Author) , Wadepohl, Hubert (Author) , Gade, Lutz H. (Author)
Format: Article (Journal)
Language:English
Published: [2015]
In: Angewandte Chemie. International edition
Year: 2015, Volume: 54, Issue: 16, Pages: 4880-4884
ISSN:1521-3773
DOI:10.1002/anie.201500141
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/anie.201500141
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201500141
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Author Notes:Christoph A. Rettenmeier, Hubert Wadepohl, and Lutz H. Gade
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Summary:Pincer-stabilized nickel(I) complexes readily react with molecular oxygen to form dinuclear 1,2-μ-peroxo-bridged nickel(II) complexes, which are the major components of a dynamic equilibrium with the corresponding mononuclear superoxo species. The peroxo complexes further react with hydrogen peroxide to give the corresponding nickel(II) hydroperoxides. One of these hitherto elusive species was characterized by X-ray diffraction for the first time [O-O bond length: 1.492(2) Å].
Item Description:Gesehen am 18.06.2020
Physical Description:Online Resource
ISSN:1521-3773
DOI:10.1002/anie.201500141

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