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Hiromasa Tanaka

Researcher at Daido University

Publications -  23
Citations -  1251

Hiromasa Tanaka is an academic researcher from Daido University. The author has contributed to research in topics: Catalysis & Pincer ligand. The author has an hindex of 13, co-authored 23 publications receiving 972 citations. Previous affiliations of Hiromasa Tanaka include Kyushu University & Kyoto University.

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Catalytic Reduction of Dinitrogen to Ammonia by Use of Molybdenum–Nitride Complexes Bearing a Tridentate Triphosphine as Catalysts

TL;DR: Newly designed and prepared molybdenum-nitride complexes bearing a mer-tridentate triphosphine as a ligand have been found to work as the most effective catalysts toward the catalytic reduction of dinitrogen to ammonia under ambient conditions.
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Catalytic formation of ammonia from molecular dinitrogen by use of dinitrogen-bridged dimolybdenum-dinitrogen complexes bearing PNP-pincer ligands: remarkable effect of substituent at PNP-pincer ligand.

TL;DR: Time profiles for the catalytic reactions indicate that the rates of the formation of ammonia and molecular dihydrogen depend on the nature of the substituent on the PNP-pincer ligand of the complexes, which is complementary in the reaction system.
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Direct Transformation of Molecular Dinitrogen into Ammonia Catalyzed by Cobalt Dinitrogen Complexes Bearing Anionic PNP Pincer Ligands

TL;DR: The direct formation of ammonia from molecular dinitrogen under mild reaction conditions was achieved by using new cobalt dinitrogens complexes bearing an anionic PNP-type pincer ligand.
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Catalytic Reduction of Molecular Dinitrogen to Ammonia and Hydrazine Using Vanadium Complexes

TL;DR: This is the first successful example of vanadium-catalyzed dinitrogen reduction under mild reaction conditions.
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Synergic Catalysis of PdCu Alloy Nanoparticles within a Macroreticular Basic Resin for Hydrogen Production from Formic Acid

TL;DR: The present catalytic system is particularly desirable for an ideal hydrogen vector in terms of potential industrial application for fuel cells and is cost-effective because of the superior catalytic activity compared with that of well-established precious PdAg or PdAu catalysts.