Nickel(II/IV) Manifold Enables Room-Temperature C(sp3)–H Functionalization

This Article demonstrates a mild oxidatively induced C­(sp3)–H activation at a high-valent Ni center. In contrast with most C­(sp3)–H activation reactions at NiII, the transformation proceeds at room temperature and generates an isolable NiIV σ-alkyl complex. Density functional theory studies show t...

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Bibliographic Details
Published in:Journal of the American Chemical Society 2019-12, Vol.141 (49), p.19513-19520
Main Authors: Roberts, Courtney C, Chong, Eugene, Kampf, Jeff W, Canty, Allan J, Ariafard, Alireza, Sanford, Melanie S
Format: Article
Language:English
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Summary:This Article demonstrates a mild oxidatively induced C­(sp3)–H activation at a high-valent Ni center. In contrast with most C­(sp3)–H activation reactions at NiII, the transformation proceeds at room temperature and generates an isolable NiIV σ-alkyl complex. Density functional theory studies show two plausible mechanisms for this C–H activation process involving triflate-assisted C–H cleavage at either a NiIV or a NiIII intermediate. The former pathway is modestly favored over the latter (by ∼3 kcal/mol). The NiIV σ-alkyl product of C–H cleavage reacts with a variety of nucleophiles to form C­(sp3)–X bonds (X = halide, oxygen, nitrogen, sulfur, or carbon). These stoichiometric transformations can be coupled using N-fluoro-2,4,6-trimethylpyridinium triflate as a terminal oxidant in conjunction with chloride as a nucleophile to achieve a proof-of-principle NiII/IV-catalyzed C­(sp3)–H functionalization reaction.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.9b11999