4.8 Article

Mechanistic Analysis of Metallaphotoredox C-N Coupling: Photocatalysis Initiates and Perpetuates Ni(I)/Ni(III) Coupling Activity

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 142, Issue 37, Pages 15830-15841

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c05901

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Funding

  1. BioLEC, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science [DE-SC0019370]
  2. Princeton Catalysis Initiative
  3. Princeton University
  4. Taylor family
  5. U.S. Department of Energy (DOE) [DE-SC0019370] Funding Source: U.S. Department of Energy (DOE)

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The combined use of reaction kinetic analysis, ultrafast spectroscopy, and stoichiometric organometallic studies has enabled the elucidation of the mechanistic underpinnings to a photocatalytic C-N cross-coupling reaction. Steady-state and ultrafast spectroscopic techniques were used to track the excited-state evolution of the employed iridium photocatalyst, determine the resting states of both iridium and nickel catalysts, and uncover the photochemical mechanism for reductive activation of the nickel cocatalyst. Stoichiometric organometallic studies along with a comprehensive kinetic study of the reaction, including rate-driving force analysis, unveiled the crucial role of photocatalysis in both initiating and sustaining a Ni(I)/Ni(III) cross-coupling mechanism. The insights gleaned from this study further enabled the discovery of a new photocatalyst providing a >30-fold rate increase.

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