4.8 Article

C-N Cross-Coupling via Photoexcitation of Nickel-Amine Complexes

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 140, Issue 24, Pages 7667-7673

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b03744

Keywords

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Funding

  1. Colorado State University
  2. National Institute of General Medical Sciences of the National Institutes of Health [R35GM119702]
  3. NIH F32 Postdoctoral Fellowship [F32GM122392]

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C-N cross-coupling is an important class of reactions with far-reaching impacts across chemistry, materials science, biology, and medicine. Transition metal complexes can elegantly orchestrate diverse aminations but typically require demanding reaction conditions, precious metal catalysts, or oxygen-sensitive procedures. Here, we introduce a mild nickel-catalyzed C-N cross-coupling methodology that operates at room temperature using an inexpensive nickel source (NiBr2 center dot 3H(2)O), is oxygen tolerant, and proceeds through direct irradiation of the nickel-amine complex. This operationally robust process was employed for the synthesis of diverse C-N-coupled products (40 examples) by irradiating a solution containing an amine, an aryl halide, and a catalytic amount of NiBr2 center dot 3H(2)O with a commercially available 365 nm LED at room temperature without added photoredox catalyst and the amine substrate serving additional roles as the ligands and base. Density functional theory calculations and kinetic isotope effect experiments were performed to elucidate the observed C-N cross-coupling reactivity.

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