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Published on: December 6, 2021
Beryllium Atom Mediated Dinitrogen Activation via Coupling with Carbon Monoxide
Guohai Deng1, Sudip Pan2,3, Guanjun Wang1
1Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysts and Innovative Materials, Fudan University, Shanghai, 200438, China.
Abstract:
The reactions of laser-ablated beryllium atoms with dinitrogen and carbon monoxide mixtures form the end-on bonded NNBeCO and side-on bonded (η2 -N2 )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 2s0 2p2 excited configuration and that the metal-ligand bonds can be described in terms of N2 →Be←CO σ donation and concomitant N2 ←Be→CO π backdonation. The results demonstrate that the activation of N2 with the N-N bond being completely cleaved can be achieved via coupling with carbon monoxide mediated by a main group atom.
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