Abstract

The new triple-bridged dinuclear cation [(η6-C6Me6)2Ru2(μ2-p-S–C6H4–OH)(μ2-PPh2)(μ2-H)]+, isolated and characterized as the tetra­fluoro­borate salt, was prepared by reacting the precursor [(η6-C6Me6)2Ru2(μ2-H)2(μ2-PPh2)](BF4) and p-hydroxy­thio­phenol in refluxing ethanol. The single-crystal X-ray structure analysis of [(η6-C12H18)2Ru2(μ2-S–C6H4–OH)(μ2-H){μ2-P(C6H5)2}](BF4) shows the formation of the meso form; despite the two stereogenic centres the complex is not chiral.

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