4.7 Article

Synthesis, Structure, and Ammonia Oxidation Catalytic Activity of Ru-NH3 Complexes Containing Multidentate Polypyridyl Ligands

期刊

INORGANIC CHEMISTRY
卷 60, 期 18, 页码 13929-13940

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.1c01528

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资金

  1. BIST Postdoctoral Fellowship Program [754510-PROBIST]
  2. BIST PhD Fellowship Programme foundation [2017 FI_B 01160]
  3. Ministerio de Ciencia, Innovacion y Universidades
  4. FEDER [PID2019-111617RB-I00]
  5. AGAUR [2017SGR-1631]
  6. Ministerio de Ciencia e Innovacion [2020-2023, CEX2019-000925-S]

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The study presented in this report focuses on investigating the catalytic activity of [Ru(tda-kappa-(NO)-O-3)(py)(2)] as a precursor for the ammonia oxidation reaction (AOR). Spectroscopic characterization of the newly synthesized complexes was performed, along with X-ray diffraction analysis of selected compounds. The study also examined the catalytic cycle proposed based on electrochemical and kinetic evidence, achieving promising turnover numbers under bulk electrolysis conditions in acetonitrile.
Ammonia (electro)oxidation with molecular catalysts is a rapidly developing topic with wide practical applications ahead. We report here the catalytic ammonia oxidation reaction (AOR) activity using [Ru(tda-kappa-(NO)-O-3)(py)(2)], 2, (tda(2-) is 2,2':6',2 ''-terpyridine-6,6 ''-dicarboxylate; py is pyridine) as a catalyst precursor. Furthermore, we also describe the rich chemistry associated with the reaction of Ru-tda and Ru-tPa (tPa(-4) is 2,2':6',2 ''-terpyridine-6,6 ''-diphosphonate) complexes with NH3 and N2H4 using [RuII(tda-kappa-N3O)(dmso)Cl] (dmso is dimethyl sulfoxide) and [RuII(tPa-kappa-N3O)(py)(2)], 8, as synthetic intermediates, respectively. All the new complexes obtained here were characterized spectroscopically by means of UV-vis and NMR. In addition, a crystal X-ray diffraction analysis was performed for complexes trans-[Ru-II(tda-kappa-N-3)(py)(2)(NH3)], 4, trans-[Ru-II(tda-kappa-N-3)(N-NH2)(py)(2)], 5, cis-[Ru-II(tda-kappa-N-3)(py)(NH3)(2)], 6 (30%), and cis-[Ru-II(tda-k-N-3)(dmso)(NH3)(2)], 7 (70%). The AOR activity associated with 2 and 8 as catalyst precursors was studied in organic and aqueous media. For 2, turnover numbers of 7.5 were achieved under bulk electrolysis conditions at an E-app = 1.4 V versus normal hydrogen electrode in acetonitrile. A catalytic cycle is proposed based on electrochemical and kinetic evidence.

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