Metal-Mediated Production of Isocyanates, R3 EN=C=O from Dinitrogen, Carbon Dioxide, and R3 ECl
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Updated: Apr 8, 2026

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Andrew J Keane1, Wesley S Farrell1, Brendan L Yonke1
1Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742 (USA).
Abstract:
A highly efficient and versatile chemical cycle has been developed for the production of isocyanates through the molecular fixation of N2 , CO2 and R3 ECl (E=C, Si, and Ge). Key steps include a 'one-pot' photolytic N-N bond cleavage of a Group 6 dinuclear dinitrogen complex with in situ trapping by R3 ECl to provide a metal terminal imido complex that can engage in simultaneous nitrene-group transfer and oxygen-atom transfer to generate an intermediate metal terminal oxo complex with release of the isocyanate product. Reaction of the oxo complex with additional equivalents of R3 ECl regenerates a metal dichloride that is the precursor for dinuclear dinitrogen starting material.
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