Novel ruthenium(II) diamine complexes |
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Authors: | Matthew D Jones John E Davies Jacek Klinowski |
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Institution: | a Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK b The Royal Institution of Great Britain, Davy Faraday Research Laboratory, 21 Albemarle Street, London W1S 4BS, UK |
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Abstract: | The complex cations Ru(C7H16N2)(C10H14)Cl]+, Ru(C7H16N2)(C6H6)Cl]+, Ru(C9H18N2)(C6H6)Cl]+, Ru(C9H18N2)(C10H14)Cl]+ and Ru(C14H16N2)(C10H14)Cl]+ have been synthesised from the reaction between the ruthenium-arene complexes with C6H6 (benzene) or C10H14 (p-cymene)] and the respective chiral diamines C7H16N2=(S)-(−)-2-aminomethyl-1-ethylpyrrolidine, C9H18N2=(S)-(+)-2-(pyrrolidinylmethyl)-pyrrolidine, or C14H16N2=(1R,2R)-(+)-1,2-diphenylethylenediamine], isolated and characterised as chloride salts using single-crystal X-ray diffraction. All complexes were fully characterised by elemental analysis, mass spectrometry, 13C and 1H NMR, and also found to exhibit catalytic activity in the transfer hydrogenation of acetophenone to 1-phenylethanol at 50 °C (enantiomeric excesses range from ca. 25% to 60%, and conversions from ca. 30% to 50%). |
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