Beryllium Atom Mediated Dinitrogen Activation via Coupling with Carbon Monoxide

The reactions of laser‐ablated beryllium atoms with dinitrogen and carbon monoxide mixtures form the end‐on bonded NNBeCO and side‐on bonded (η(2)‐N(2))BeCO isomers in solid argon, which are predicted by quantum chemical calculations to be almost isoenergetic. The end‐on bonded complex has a triplet ground state while the side‐on bonded isomer has a singlet electronic ground state. The complexes rearrange to the energetically lowest lying NBeNCO isomer upon visible light excitation, which is characterized to be an isocyanate complex of a nitrene derivative with a triplet electronic ground state. A bonding analysis using a charge‐ and energy decomposition procedure reveals that the electronic reference state of Be in the NNBeCO isomers has an 2s(0)2p(2) excited configuration and that the metal‐ligand bonds can be described in terms of N(2)→Be←CO σ donation and concomitant N(2)←Be→CO π backdonation. The results demonstrate that the activation of N(2) with the N−N bond being completely cleaved can be achieved via coupling with carbon monoxide mediated by a main group atom.