Synthesis and characterization of isomeric 4- and 8-(σ–CHCHPh)-closo-ruthenacarboranes with η3:η2-phosphacarbocyclic ligand

Reactions of [3,3-(PPh3)2-3-Cl-3-H-3,1,2-closo-RuC2B9H11] (1) and its exo-nido isomer [exo-5,6,10-{Ru(Ph3P)2Cl}-5,6,10-(μ-H)3-10-H-7,8-nido-C2B9H8] (2) with NH4PF6 in methanol or ethanol solution followed by heating in the presence of an excess of phenylacetylene (3) affords a mixture of two isomeric closo species [3,3-{(1′-3′-η3):(5′,6′-η2)-ortho-C6H4PPh2CHC(Ph)CHCHPh}-8-(σ–CHCHPh)-3,1,2-closo-RuC2B9H10] (4) and [3,3-{(1′-3′-η3):(5′,6′-η2)-ortho-C6H4PPh2CHC(Ph)CHCHPh}-4-(σ–CHCHPh)-3,1,2-closo-RuC2B9H10] (5) in which boron vertexes in β- and α-sites with respect to the cage carbons bear the (E)–CHCHPh group. The X-ray diffraction study of 4 together with the multinuclear NMR data for 4 and 5 revealed that such an unusual η3:η2-phosphacarbocyclic ligand in both isomeric complexes is formed by specific insertion of the initially metal-bound PPh3 group into the chain of two alkyne molecules coupled in a “head-to-tail” fashion around the metal vertex.

Thermal treatment of [3,3-(PPh3)2-3-Cl-3-H-3,1,2-closo-RuC2B9H11] or its exo-nido isomer [exo-5,6,10-{Ru(Ph3P)2Cl}-5,6,10-(μ-H)3-10-H-7,8-nido-C2B9H8] in MeOH or EtOH solution with an excess of PhCCH in the presence of NH4PF6 affords two isomeric closo species [3,3-{(1′-3′-η3):(5′,6′-η2)-ortho-C6H4PPh2CHC(Ph)CHCHPh}-8-(σ-CHCHPh)-3,1,2-closo-RuC2B9H10] and [3,3-{(1′-3′-η3):(5′,6′-η2)-ortho-C6H4PPh2CHC(Ph)CHCHPh}-4-(σ–CHCHPh)-3,1,2-closo-RuC2B9H10] with an unusual η3:η2-phosphacarbocyclic ligand at the metal vertex.Figure optionsDownload as PowerPoint slideHighlights
► Novel closo-ruthenacarboranes with an unusual phosphacarbocyclic ligand are described.
► Specific insertion of the PPh3 group into the two “head-to-tail” coupled alkynes occurs.
► The X-ray diffraction study of one of these species has been performed.