Ammonia Synthesis from a Pincer Ruthenium Nitride via Metal-Ligand Cooperative Proton-Coupled Electron Transfer

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American Chemical Society

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The conversion of metal nitride complexes to ammonia may be essential to dinitrogen fixation. We report a new reduction pathway that utilizes ligating acids and metal-ligand cooperation to effect this conversion without external reductants. Weak acids such as 4-methoxybenzoic acid and 2-pyridone react with nitride complex [(H-PNP)RuN]+ (H-PNP = HN(CH2CH2PtBu2)2) to generate octahedral ammine complexes that are κ2-chelated by the conjugate base. Experimental and computational mechanistic studies reveal the important role of Lewis basic sites proximal to the acidic proton in facilitating protonation of the nitride. The subsequent reduction to ammonia is enabled by intramolecular 2H+/2e- proton-coupled electron transfer from the saturated pincer ligand backbone. © 2017 American Chemical Society.

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Ammonia, Chelation, Electron transitions, Ligands, Nitrides, Refractory metal compounds, Dipyrone, Hydrogen, Metal, Ruthenium, Ammine complexes, Ammonia synthesis, Lewis basic site, Mechanistic studies, Metal nitrides, Pincer ligands, Proton coupled electron transfers, Subsequent reduction, Article, Chemical structure, Cyclic potentiometry, Electron transport, Heteronuclear single quantum coherence, Hydrogenation, Isomerization, Proton nuclear magnetic resonance, Proton transport, Synthesis, X ray crystallography, Ruthenium compounds

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