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• W3214036706 abstract "Herein we report the preparation of a series of Ru(II) complexes featuring alpha-iminopyridine ligands bearing thioether functionality (NNS^R, where R = Me, CH₂Ph, Ph). Metallation using (<i>p</i> cymene)RuCl dimer permits access to (k²-N,N)Ru complexes in which the thioether moiety remains uncoordinated. In the presence of a strong field ligand such as acetonitrile or triphenylphosphine, the p-cymene moiety is displaced, and the ligand adopts a k³-N,N,S binding mode. These complexes are characterized using a combination of solution and solid state methods, including the crystal structure of [(NNS^Me)Ru(NCMe)₂Cl]Cl. The k²-N,N Ru(II) complexes are shown to serve as efficient precatalysts for the oxidation of sec-phenethyl alcohol at 5 mol% loadings, using a variety of external oxidants and solvents. The complex bearing an S-Ph donor was found to be the most active of those surveyed, suggesting that the thioether donor plays an active role in catalyst speciation for this transformation." @default.
• W3214036706 created "2021-11-22" @default.
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• W3214036706 date "2019-08-21" @default.
• W3214036706 modified "2023-10-17" @default.
• W3214036706 title "Ruthenium(II) Complexes Bearing Thioether-Appended α- Iminopyridine Ligands: Arene Precursors Permit Access to K2-N,N and K3-N,N,S Complexes" @default.
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• W3214036706 doi "https://doi.org/10.26434/chemrxiv.9693506.v1" @default.
• W3214036706 hasPublicationYear "2019" @default.
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