Dinitrogen Cleavage and Hydrogenation by a Uranium Hydride Complex Enabled through Metal–Ligand Cooperativity

Dinitrogen cleavage and hydrogenation by metal hydride complexes are relevant to both enzymatic and industrial dinitrogen (N<sub>2</sub>) fixation but remain limited to a few examples. Here, we report the cleavage and functionalization of N<sub>2</sub> mediated by a pincer ligand-supported diuranium(IV) hydride complex [{(Dipp-NON)U<sup>IV</sup>(η<sup>4</sup>-HDipp)}(<i>μ-</i>H){(η<sup>6</sup>-Dipp)U<sup>IV</sup>(NON-Dipp)}], <b>1</b>. In this complex, a total of six electrons and two protons are stored in two flanking arms of the bis(anilido)xanthene scaffolds and in the bridging hydride, which are stabilized by two uranium(IV) centers. The reaction of complex <b>1</b> with dinitrogen results in concomitant N<sub>2</sub> cleavage and functionalization, affording the bis-imido complex [{(Dipp<sub>2</sub>-NON)U<sup>IV</sup>}<sub>2</sub>(μ-NH)<sub>2</sub>], <b>3</b>, via an unprecedented cooperative metal-ligand pathway and without involving a change of the uranium oxidation state during the overall transformation.

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Journal
Journal of the American Chemical Society
Published
2026-02-25
DOI
https://doi.org/10.1021/jacs.6c00478
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
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article

Dinitrogen Cleavage and Hydrogenation by a Uranium Hydride Complex Enabled through Metal–Ligand Cooperativity

R. Scopelliti, Mikhail S. Batov, Ivica Zivkovic, Marinella Mazzanti et al.
Journal of the American Chemical Society
Asymmetric Hydrogenation and Catalysis
article

Dinitrogen Cleavage and Hydrogenation by a Uranium Hydride Complex Enabled through Metal–Ligand Cooperativity

R. Scopelliti, Mikhail S. Batov, Ivica Zivkovic, Marinella Mazzanti, Yue Pang, Thayalan Rajeshkumar, Laurent Maron
article en

Abstract

Dinitrogen cleavage and hydrogenation by metal hydride complexes are relevant to both enzymatic and industrial dinitrogen (N<sub>2</sub>) fixation but remain limited to a few examples. Here, we report the cleavage and functionalization of N<sub>2</sub> mediated by a pincer ligand-supported diuranium(IV) hydride complex [{(Dipp-NON)U<sup>IV</sup>(η<sup>4</sup>-HDipp)}(<i>μ-</i>H){(η<sup>6</sup>-Dipp)U<sup>IV</sup>(NON-Dipp)}], <b>1</b>. In this complex, a total of six electrons and two protons are stored in two flanking arms of the bis(anilido)xanthene scaffolds and in the bridging hydride, which are stabilized by two uranium(IV) centers. The reaction of complex <b>1</b> with dinitrogen results in concomitant N<sub>2</sub> cleavage and functionalization, affording the bis-imido complex [{(Dipp<sub>2</sub>-NON)U<sup>IV</sup>}<sub>2</sub>(μ-NH)<sub>2</sub>], <b>3</b>, via an unprecedented cooperative metal-ligand pathway and without involving a change of the uranium oxidation state during the overall transformation.

Journal of the American Chemical SocietyVol. 148(9)
Centre National de la Recherche Scientifique (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Institut National des Sciences Appliquées de Toulouse (FR), Institut de Chimie (FR), Institute of Magnetism (UA), École Polytechnique Fédérale de Lausanne (CH)
Openalex Percentile: Top 45%
Asymmetric Hydrogenation and Catalysis
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