Article Dans Une Revue Organometallics Année : 2026

Ligand-Directed Divergent Selectivities in Cobalt-Catalyzed Transfer Hydrogenation of Quinolines: Insights from Experiment and Theory

Sélectivités divergentes ligand-dirigées dans des hydrogénations par transfert catalysées au cobalt sur des quinolines : Perspectives expérimentales et théoriques

Résumé

The selective hydrogenation of quinolines is a valuable transformation for accessing functionalized N-heterocycles but achieving control over the degree of reduction under mild and sustainable conditions remains challenging. Herein, we report the transfer hydrogenation of quinoline using one equivalent of ammonia-borane (NH3BH3) at room temperature, catalyzed by two well-defined cobalt hydride complexes: HCo(PMe3)4 and H3Co(PPh3)3. The Co(I) hydride complex HCo(PMe3)4 selectively affords 1,2-dihydroquinoline (1,2-DHQ), while the Co(III) trihydride H3Co(PPh3)3, for which we report the first X-ray crystal structure, yields the doubly reduced tetrahydroquinoline (THQ). A detailed mechanistic study combining DFT calculations and deuterium labeling experiments reveals that the phosphine ligand plays a decisive role in directing the reaction selectivity: the bulky and less donating PPh3 ligands facilitate isomerization of 1,2-DHQ to 1,4-DHQ, whereas the PMe3 ligand favors the halting at the 1,2-DHQ stage. These results provide a rare case of ligand-controlled divergence in base-metal-catalyzed transfer hydrogenation and highlight the potential of cobalt hydride complexes for tunable and selective N-heteroarene reductions.

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hal-05582910 , version 1 (07-04-2026)

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Valentin Poirier, Cassandre C Bories, Marion Barbazanges, Jérémy Forté, Alexandre Pradal, et al.. Ligand-Directed Divergent Selectivities in Cobalt-Catalyzed Transfer Hydrogenation of Quinolines: Insights from Experiment and Theory. Organometallics, 2026, 45, pp.367. ⟨10.1021/acs.organomet.5c00495⟩. ⟨hal-05582910⟩
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