C─C Bond Formation via Reductive Elimination at Rare Earth Centers.

Reductive elimination is one of the most important elementary reactions employed for constructing various chemical bonds in transition metal complex-mediated transformations. However, due to the lack of two-electron transfer, rare earth (RE) centers have been considered incapable of promoting reductive elimination, thus limiting the reactivity of RE complexes and their applications in synthetic chemistry. In the presented study, we demonstrated the reactions of β-diketiminate-supported dialkyl RE(III) complexes (L-κN,N')RE(III)(CHSiMe)(THF) (1-RE, RE = Y, Er, Yb, and Lu; L = {[(2,4,6-MeCH)NCMe]CH}) with azobenzene at ambient conditions, resulting in the formations of (L-κN,N')RE(III)(η-cis-PhNNPh)(THF) (2-RE) and 2-[(trimethylsilyl)methyl]azobenzene (I) via a reductive elimination-powered pathway. The key intermediate (L-κN,N')Lu(III)(PhNNCH-κN,C)(CHSiMe) (3-Lu), which is formed via ortho-H deprotonation in azobenzene by the (trimethylsilyl)methyl group in 1-Lu, was isolated and structurally identified. The computational studies indicate that the subsequent η-coordination of a cis-azobenzene to the RE(III) centers in this intermediate triggers the reductive elimination between the (trimethylsilyl)methyl group and the neighboring PhNNCH-κN,C group, consequently enabling the C─C cross-coupling that affords product I. In this elementary process, the two N═N π*-orbitals mainly act as the energetically accessible acceptors for the two electrons being transferred, thereby facilitating the reductive elimination by avoiding the thermodynamically unfavorable 2e-reductions of RE centers.