Iron-dinitrogen complexes bearing methyl- and phenyl-substituted pyrrole-based anionic PNP-type pincer ligands are prepared and characterized by X-ray analysis. The former complex is found to work as a more effective catalyst than that bearing a non-substituted PNP-type pincer ligand toward the transformation of nitrogen gas into ammonia and hydrazine under mild reaction conditions.
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http://dx.doi.org/10.1039/c7cc06987a | DOI Listing |
Dalton Trans
October 2023
Department of Applied Chemistry, School of Engineering, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.
Angew Chem Int Ed Engl
October 2023
Department of Applied Chemistry, School of Engineering, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan.
Chem Sci
March 2023
Max Planck Institute for Chemical Energy Conversion Stiftstr. 34-36, 45470 Mülheim an der Ruhr Germany
The stepwise catalytic reduction of carbon dioxide (CO) to formic acid, formaldehyde, and methanol opens non-fossil pathways to important platform chemicals. The present article aims at identifying molecular control parameters to steer the selectivity to the three distinct reduction levels using organometallic catalysts of earth-abundant first-row metals. A linear scaling relationship was developed to map the intrinsic reactivity of 3d transition metal pincer complexes to their activity and selectivity in CO hydrosilylation.
View Article and Find Full Text PDFDalton Trans
November 2022
Departament de Química Inorgànica i Orgànica. Secció de Química Inorgànica. Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona, Spain.
The synthesis and characterization of two dinuclear and five tetranuclear gold(I) complexes bearing the 2,6-bis(diphenylphosphinomethyl)pyridine diphosphane ligand (DPPMPY) are herein reported. The reaction between the dinuclear complexes, DPPMPY(AuCl) (1) or DPPMPY(AuBr) (2), with 1 or 2 equivalents of Ag salts yielded five tetranuclear gold(I) complexes, DPPMPYAuX (3-7), differing in the terminal ancillary ligands (X = Cl, Br, acetonitrile) and the counter ions (SbF or BF). The structures of complexes 1, 2, 3, and 5 were confirmed by single-crystal X-ray diffraction studies.
View Article and Find Full Text PDFChem Commun (Camb)
October 2022
Department of Chemistry, and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8, Canada.
While classical cross-couplings are dominated by palladium and nickel catalysts, cobalt-based catalysts have shown unique advantages for such cross-coupling reactions in terms of higher catalytic activity and lower toxicity. Herein, we describe a novel cobalt-catalyzed alkyl-alkyl cross-coupling reaction of hydrazone with alkyl halides under mild reaction conditions, where the use of a PNP-type pincer ligand is essential for catalysis. Both aldehyde and ketone hydrazones are compatible with this reaction, giving a series of C(sp)-C(sp) coupling products in moderate to good yields.
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