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Demonstrates an iron-mediated method for carbene generation from diazo compounds, suggesting a new mechanism for N2 extrusion.
One of the main pathways to (metal)carbene formation proceeds via the decomposition of diazo compounds, which can be triggered thermally, photochemically, or by transition-metal mediation. An alternative pathway for carbene generation from diazo compounds is the “pulling-out” N 2 by different reagents. Herein, we report an iron-mediated strategy for the homolytic cleavage of C═N bond in diazo compounds, enabling the generation of free carbenes and iron–dinitrogen complexes under mild conditions. The corresponding Fe–diazo intermediates were isolated and fully characterized by X-ray crystallography and NMR spectroscopy. Homolytic C–N bond cleavage occurs upon warming, affording a persistent (phosphino)(silyl)carbene. The kinetics of this process were further elucidated by Eyring analysis. Computational modeling highlighted the critical role of Fe → N π-backdonation in cleaving the C═N π bond. These findings establish a new mechanistic framework for metal-assisted dinitrogen extrusion from diazo compounds and offer valuable insights into controlled carbene generation.
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Cui et al. (2026) studied this question.
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