Reactivity of thiophosphinous acid bound to ruthenium

The thiophosphinous acid coordinated to ruthenium through the phosphorus atom in [CpRu(PPh3)2(PH2SH)]CF3SO3 (1) is deprotonated in the presence of proton sponge to yield the neutral compound [CpRu(PPh3)2(PH2S)] (2), where the thiophosphinite, PH2S−, anion remains bound to the metal through the phosphorus atom. The parent complex 1 is easily restored in the presence of a weak acid. The sulfur of the coordinated anion may be alkylated with CF3SO3Me to yield [CpRu(PPh3)2(PH2SCH3)]CF3SO3 (3), the methyl thioester of the acid being bound to ruthenium through the phosphorus. The new compounds have been characterized by elemental analyses, IR and multinuclear NMR spectroscopy. The crystal structure of 2 · CH3CN has been determined by X-ray diffraction methods.

The thiophosphinous acid, PH2SH, stabilized through coordination to the CpRu(PPh3)2 platform, is reversibly deprotonated to yield the neutral compound [CpRu(PPh3)2(PH2S)], where the thiophosphinite anion, PH2S−, remains bound to the metal through the phosphorus atom. The sulfur of the coordinated anion may be alkylated to yield [CpRu(PPh3)2(PH2SCH3)]CF3SO3.Figure optionsDownload as PowerPoint slide