Ketone transfer hydrogenation reactions catalyzed by catalysts based on a phosphinite ligand


Karakaş D.E. Rafikova K. Baysal A. Meriç N. Zazybin A. Kayan C. Işik U. Saparbaykyzy I.S. Durap F. Aydemir M.
2022Taylor and Francis Ltd.

Journal of Coordination Chemistry
2022#75Issue 3-4493 - 506 pp.

Reaction of (±)-1-(2-furyl) ethanol with an equivalent Ph2PCl in the presence of Et3N proceeds in dry toluene under an argon atmosphere to give 1-(furan-2-yl)ethyl diphenylphosphinite (1) in good yield. Mononuclear complexes [dichloro(η6-p-cymene)(1-furan-2-ylethyl diphenylphosphinite)ruthenium(II)] (2), [dichloro(η6-benzene)(1-furan-2-ylethyl diphenylphosphinite)ruthenium(II)] (3), [chloro(η4-1,5-cyclooctadiene)(1-furan-2-ylethyl diphenylphosphinite)rhodium(I)] (4) and [dichloro(η5-pentamethylcyclopentadienyl)(1-furan-2-ylethyl diphenylphosphinite)iridium(III)] (5) were synthesized and characterized by microanalysis, infrared, MS, and NMR spectroscopies. The complexes are employed as catalysts in transfer hydrogenation of aromatic ketones. The complexes catalyzed reduction of a variety of aromatic ketone substrates bearing electron-withdrawing or donating substituents with very high conversion rates (up to 99%); 5 was the most efficient catalyst for the transfer hydrogenation of ketones.

iridium , ketone , phosphinite ligand , Transfer hydrogenation , transition metal

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Science and Technology Application and Research Center (SIUBTAM), Siirt University, Siirt, Turkey
Institute of Chemical and Biological Technologies, Satbayev University, Almaty, Kazakhstan
School of Chemical Engineering, Kazakh-British Technical University, Almaty, Kazakhstan
Faculty of Science, Department of Chemistry, Dicle University, Diyarbakir, Turkey

Science and Technology Application and Research Center (SIUBTAM)
Institute of Chemical and Biological Technologies
School of Chemical Engineering
Faculty of Science

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