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dc.contributor.authorGichumbi, Joel M.
dc.contributor.authorFriedrich, Holger B.
dc.contributor.authorOmondi, Bernard
dc.date.accessioned2020-10-30T07:07:31Z
dc.date.available2020-10-30T07:07:31Z
dc.date.issued2018-12-25
dc.identifier.citationJournal Journal of Coordination Chemistry Volume 72 - Issue 1 Pages 135-147en_US
dc.identifier.urihttps://doi.org/10.1080/00958972.2018.1548702
dc.identifier.urihttp://repository.chuka.ac.ke/handle/chuka/4915
dc.description.abstractNew water-soluble complexes [(η6-C6H6)RuCl(C5H4N-2-CH = N-R)]Cl (1) (with R = 4-hydroxymethylphenyl (a), 2,4-dichlorophenyl (b), 2-fluorophenyl (c), 3-carboxyphenyl (d)) have been synthesized by reacting [(η6-C6H6)Ru(μ-Cl)Cl]2 with the N,N′-bidentate ligands in a 1:2 ratio. Full characterization of all complexes was accomplished using 1H and 13C NMR, elemental analyses, UV-Vis spectroscopy, IR spectroscopy and single crystal X-ray crystallography for determination of the structure of 1d, as 1d•4H2O. The single crystal structure confirmed coordination of the ligand to the ruthenium(II) center leading to a structure commonly described as a pseudo-octahedral, three-legged piano stool. The geometry around the Ru(II) center is such that the arene ring occupies the apex of the stool while the N,N′-bidentate ligand and a chloride occupy the base of the stool. The synthesized Ru(II) complexes were tested as catalysts for oxidation of styrene using NaIO4 as a co-oxidant in a biphasic system. All complexes were active, giving good yields of benzaldehyde. Catalyst 1c was later investigated for olefin oxidation and gave high yields of the corresponding aldehydes as the major products in all cases.en_US
dc.language.isoenen_US
dc.subjectWater-solubleen_US
dc.subjectruthenium-areneen_US
dc.subjectN,N′-bidentate ligandsen_US
dc.subjectolefin oxidationen_US
dc.subjectX-ray structureen_US
dc.titleSynthesis and characterization of water-soluble arene- ruthenium complexes and their application in biphasic olefin oxidationen_US
dc.typeArticleen_US


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