Abstract
Catalytic N-N coupling is a valuable transformation for chemical synthesis and energy conversion. Here, mechanistic studies are presented for two related copper-catalyzed oxidative aerobic N-N coupling reactions, one involving the synthesis of a pharmaceutically relevant triazole and the other relevant to the oxidative conversion of ammonia to hydrazine. Analysis of catalytic and stoichiometric N-N coupling reactions support an "oxidase"-type catalytic mechanism with two redox half-reactions: (1) aerobic oxidation of a CuI catalyst and (2) CuII-promoted N-N coupling. Both reactions feature turnover-limiting oxidation of CuI by O2, and this step is inhibited by the N-H substrate(s). The results highlight the unexpected facility of the N-N coupling step and establish a foundation for development of improved catalysts for these transformations.
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CITATION STYLE
Ryan, M. C., Kim, Y. J., Gerken, J. B., Wang, F., Aristov, M. M., Martinelli, J. R., & Stahl, S. S. (2020). Mechanistic insights into copper-catalyzed aerobic oxidative coupling of N-N bonds. Chemical Science, 11(4), 1170–1175. https://doi.org/10.1039/c9sc04305e
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