New Scandium Borylimido Chemistry: Synthesis, Bonding, and Reactivity.

We report a combined synthetic, mechanistic, and theoretical study of the first borylimido complex of a rare earth metal, (NacNac)Sc{NB(NAr'CH)} (25, Ar' = 2,6-CHPr, NacNac = Ar'NC(Me)CHC(Me)NCHCHNMe). Thermolysis of the methyl-borylamide (NacNac)Sc(Me){NHB(NAr'CH)} (18) generated transient imide 25 via rate-determining, first-order methane elimination (KIE ≈ 8.7). In the absence of external substrate, 25 underwent a reversible cyclometalation reaction (sp C-H bond addition to Sc═N) with a methyl group of the NacNac ligand forming {MeC(NCHPrCH(Me)CH)CHC(Me)NCHCHNMe}Sc{NHB(NAr'CH)} (21). In the presence of pyridine or DMAP, reversible sp C-H bond activation occurred, forming orthometalated complexes (NacNac)Sc{NHB(NAr'CH)}(η-4-NCHR) (R = H or NMe). In situ reaction of 25 with HCCTol gives irreversible sp C-H bond activation under kinetic control, and with MeCCPh [2+2] cycloaddition to Sc═N takes place. These reactions represent the first substrate activation processes for any metal-bound borylimide. The bonding in 25 and the mechanism and thermodynamics of the reactions have been studied using density functional theory (DFT), supported by quantum theory of atoms in molecules and natural bond orbital analysis. Although the borylimido and arylimido dianions studied here are formally isoelectronic and possess comparable frontier molecular orbitals, the borylimido ligand is both a better π-donor and σ-donor, forming stronger and shorter metal-nitrogen bonds with somewhat reduced ionicity. Despite this, reactions of these types of borylimides with C-H or C≡C bonds are all more exothermic and more strongly activating than for the corresponding arylimides. DFT calculations on model systems of differing steric bulk unpicked the underlying thermodynamic factors controlling the reactions of 25 and its reaction partners, and a detailed comparison was made with the previously described arylimido homologues.