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pH-Dependent Selective Transfer Hydrogenation of α,β-Unsaturated Carbonyls in Aqueous Media Utilizing Half-Sandwich Ruthenium(II) Complexes

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posted on 15.01.2007, 00:00 authored by Charles A. Mebi, Radhika P. Nair, Brian J. Frost
Half-sandwich ruthenium(II) PTA complexes bearing the 1,2-dihydropentalenyl (C8H9-, Dp) and indenyl (C9H7-, Ind) ancillary ligands have been synthesized and characterized using multinuclear NMR spectroscopy and X-ray crystallography. The complexes DpRu(PTA)(PPh3)Cl, DpRu(PTA)2Cl, IndRu(PTA)(PPh3)Cl, and [IndRu(PTA)2(PPh3)]Cl were obtained in good to excellent yields. The solid-state structures of these compounds exhibit piano stool geometries with η5-coordination of the indenyl and dihydropentalenyl moieties. DpRu(PTA)2Cl is water-soluble (S25°C = 43 mg/mL), while the mixed phosphine compounds are slightly soluble in acidic solutions. The Ru−H complexes, Cp‘Ru(PTA)(PPh3)H (Cp‘ = Ind, Cp), have been synthesized in good yield and spectroscopically and structurally characterized. The ruthenium hydrides undergo an H/D exchange reaction with CD3OD with relative rates CpRu(PTA)(PPh3)H ≫ IndRu(PTA)(PPh3)H > CpRu(PTA)2H. The air-stable Cp‘Ru(PTA)(PR3)Cl complexes (Cp‘ = Cp, Dp, Ind; PR3 = PPh3 or PTA) exhibit activity in the regioselective transfer hydrogenation of α,β-unsaturated carbonyls in aqueous media with HCOONa, HCOOH, or isopropanol/Na2CO3 serving as the hydrogen source. They were found to be effective in the selective reduction of the carbonyl functionality of cinnamaldehyde and the CC bond of benzylidene acetone and chalcone. IndRu(PTA)(PPh3)Cl was less active than Cp‘Ru(PTA)(PPh3)Cl (Cp‘ = Cp or Dp). Results of the transfer hydrogenation of unsaturated substrates using CpRu(PTA)(PPh3)H are also reported.