A titanium redox-switch enables reversible C-C bond forming and splitting reactions.

Using an Earth-abundant transition metal to mediate formation and splitting of C-C σ-bonds, in response to electrical stimuli, constitutes a promising strategy to construct complex organic skeletons. Here, we showcase how [ n Bu4N][N3] reacts with an isocyanide adduct of a tetrahedral and high-spin TiII complex, [(Tp tBu,Me)TiCl] (1), to enact N-atom transfer, C-N bond formation, and C-C coupling, to form a dinuclear complex, [(Tp tBu,Me)Ti{AdN(N)C-C(N)NAd}Ti(Tp tBu,Me)] (3), with two TiIII ions bridged by a disubstituted oxalimidamide ligand ( n Bu = n-butyl, Tp tBu,Me = hydrotris(3-tert-butyl-5-methylpyrazol-1-yl)borate, Ad = 1-adamantyl). Magnetic and computational studies reveal two magnetically isolated d1 TiIII ions, and electrochemical studies unravel a reversible two-electron oxidation at -0.87 V vs. [FeCp2]0/+. Despite these observations, chemical oxidation of 3, ultimately, leads to rupture of the oxalimidamide moiety with C-C bond splitting to form [(Tp tBu,Me)Ti{1,3-μ2-AdNCN}2Ti(Tp tBu,Me)][B(C6F5)4]2 (4), which displays an antiferromagnetically coupled Ti2 III,III configuration, mediated by superexchange through its bridging carbodiimide ligands. A comparative reactivity study of isocyanide toward a transient vanadium nitride [(Tp tBu,Me)V[triple bond, length as m-dash]N(THF)] (5) gives further insight into the structure of putative intermediates involved in the coupling sequence.