Mechanistic Studies on the Bismuth-Catalyzed Transfer Hydrogenation of Azoarenes

Organobismuth-catalyzed transfer hydrogenation has recently been disclosed as an example of low-valent Bi redox catalysis. However, its mechanistic details have remained speculative. Herein, we report experimental and computational studies that provide mechanistic insights into a Bi-catalyzed transfer hydrogenation of azoarenes using p-trifluoromethylphenol (4) and pinacolborane (5) as hydrogen sources. A kinetic analysis elucidated the rate orders in all components in the catalytic reaction and determined that 1 a (2,6-bis[N-(tert-butyl)iminomethyl]phenylbismuth) is the resting state. In the transfer hydrogenation of azobenzene using 1 a and 4, an equilibrium between 1 a and 1 a & sdot; [OAr]2 (Ar=p-CF3-C6H4) is observed, and its thermodynamic parameters are established through variable-temperature NMR studies. Additionally, pKa-gated reactivity is observed, validating the proton-coupled nature of the transformation. The ensuing 1 a & sdot; [OAr]2 is crystallographically characterized, and shown to be rapidly reduced to 1 a in the presence of 5. DFT calculations indicate a rate-limiting transition state in which the initial N-H bond is formed via concerted proton transfer upon nucleophilic addition of 1 a to a hydrogen-bonded adduct of azobenzene and 4. These studies guided the discovery of a second-generation Bi catalyst, the rate-limiting transition state of which is lower in energy, leading to catalytic transfer hydrogenation at lower catalyst loadings and at cryogenic temperature. We report a combined experimental and computational study of the bismuth-catalyzed transfer hydrogenation of azoarenes. With the protocol using p-trifluoromethylphenol and pinacolborane, we identified the role of protic and hydridic hydrogens through kinetic analysis and reactivity studies. The possibility of Bi-ligand cooperativity was assessed through isotope labeling experiments. This work validates the notion of Bi(I)/Bi(III) redox cycling.+image