Chromium Nitride Umpolung Tuned by the Locus of Oxidation

Abstract

Oxidation of a series of CrV nitride salen complexes (CrVNSalR) with different para-phenolate substituents (R = CF3, tBu, NMe2) was investigated to determine how the locus of oxidation (either metal or ligand) dictates reactivity at the nitride. Para-phenolate substituents were chosen to provide maximum variation in the electron-donating ability of the tetradentate ligand at a site remote from the metal coordination sphere. We show that one-electron oxidation affords CrVI nitrides ([CrVINSalR]+; R = CF3, tBu) and a localized CrV nitride phenoxyl radical for the more electron-donating NMe2 substituent ([CrVNSalNMe2]•+). The facile nitride homocoupling observed for the MnVI analogues was significantly attenuated for the CrVI complexes due to a smaller increase in nitride character in the M≡N π* orbitals for Cr relative to Mn. Upon oxidation, both the calculated nitride natural population analysis (NPA) charge and energy of molecular orbitals associated with the {Cr≡N} unit change to a lesser extent for the CrV ligand radical derivative ([CrVNSalNMe2]•+) in comparison to the CrVI derivatives ([CrVINSalR]+; R = CF3, tBu). As a result, [CrVNSalNMe2]•+ reacts with B(C6F5)3, thus exhibiting similar nucleophilic reactivity to the neutral CrV nitride derivatives. In contrast, the CrVI derivatives ([CrVINSalR]+; R = CF3, tBu) act as electrophiles, displaying facile reactivity with PPh3 and no reaction with B(C6F5)3. Thus, while oxidation to the ligand radical does not change the reactivity profile, metal-based oxidation to CrVI results in umpolung, a switch from nucleophilic to electrophilic reactivity at the terminal nitride.