This article describes the synthesis and reactivity of Ni II (Phpy) 2 (Phpy = 2-phenylpyridine) with a variety of oxidants, including O 2, Br 2, PhICl 2, N -fluoropyridinium salts, Cu II salts, and N -halosuccinimides. High-oxidation-state Ni intermediates were not detected in any of these transformations. In all cases, the major organic product resulted from oxidatively induced C−C bond formation to generate the Phpy−Phpy dimer. Traces (2−16%) of organic products resulting from C−O, C−Br, C−Cl, and C−N bond-forming reductive elimination were also observed.
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Higgs et al. (2010) studied this question.
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