Rapid Intermolecular C-H Activation of Aromatic Substrates at a Cationic, Electrophilic Molybdenum(VI) Nitrido...

When the cationic, octahedral terminal nitrido complex of Mo(VI) supported by a diborate pentadentate ligand is generated in the absence of trapping nucleophiles, it activates the C(sp²)-H bonds of simple arenes, forming the cationic imido complexes [[^ArMo^V]═NR]⁺ (R = H; PhX, X = H, o,m,p-F). Density Functional Theory computations and experimental studies support a novel mechanism with homolytic aromatic substitution character, wherein electrophilic attack of the arene π system initiates N-C bond formation, but use of electrons from the Mo≡N triple bond completes bond formation through an open-shell singlet transition state that formally reduces the metal center to Mo(V) and imbues the arene ring with radical character. This transition state is enthalpically 15 kcal mol^-1 lower in energy than the "Wheland-type" transition state common to electrophilic aromatic substitution paths proposed in related systems. Subsequent intramolecular transfer of the arene hydrogen to the imido nitrogen atom leads to the cationic Mo(IV) anilido complex [[^ArMo^IV]-NHPh]⁺, which reacts with available [[^ArMo^VI]≡N]⁺ by a proton-coupled electron transfer step to generate the 1:1 mixture of imido products [[^ArMo^V]=NR]⁺ (R = H; C₆H₄X, X = H, o,m,p-F). This second phase of the mechanism is supported computationally and by a crossover experiment and is driven by significant coordination-induced bond weakening (CIBW) in the N-H bond of the [[^ArMo^IV]-NHPh]⁺. The novel mechanism of C-H addition to the electrophilic terminal nitrido opens new low energy pathways for the development of systems capable of catalytic nitrogen atom transfer to C-H bonds.