Cobalt-Catalyzed C(sp<sup>2</sup>)–CN Bond Activation: Cross-Electrophile Coupling for Biaryl Formation and Mechanistic Insight
Céline Dorval, Maxime Tricoire, Jeanne‐Marie Begouin, Vincent Gandon, Corinne Gosmini
Abstract
Herein, we report a cross-electrophile coupling of benzonitrile derivatives and aryl halides with a simple cobalt-based catalytic system under mild conditions to form biaryl compounds. Even though the cobalt catalyst is able to activate the C(sp 2 )–CN bond alone, the use of the AlMe 3 Lewis acid enhances the reactivity of benzonitriles and improves the cross-selectivity with barely any influence on the functional group compatibility. X-ray structure determination of an original low-valent cobalt species combined with catalytic and stoichiometric reactions reveals a catalytically active cobalt(I) species toward the aryl halide partner. On the other hand, experimental insights, including cyclic voltammetry experiments, suggest the involvement of a cobalt complex of a lower oxidation state to activate the benzonitrile derivative. Finally, density functional theory calculations support the proposed mechanistic cycle involving two low-valent cobalt species of different oxidation states to perform the reaction.