| Abstract
| - Treatment of dinuclear Ru(II)/Ru(IV) half-sandwich complexes (p-cymene)Ru(μ-E2)Ru(S2C2B10H10)2, (E = S, 1a; E = Se, 1b) with alkynes affords addition Ru(II)/Ru(II) complexes, (p-cymene)Ru(μ-E2)Ru(S2C2B10H10)2(R1C=CR2), (2a−7a, 2b−7b), and an unprecedented tetranuclear mixed-valent Ru(IV)Ru(II)3 complex, (p-cymene)2Ru4S4(S2C2B10H10)4(HC=CFc), 8a.
- Treatment of 1a and 1b with phenylacetylene, 1,4-diethynylbenzene, and ethynylferrocene affords addition complexes, (p-cymene)Ru(μ-E2)Ru(S2C2B10H10)2(R1C=CR2), (R1 = Ph (H), R2 = H (Ph), 2a, 2b, 3a, 3b; R1 = −Ph−CCH (H), R2 = H (−Ph−CCH), 4a, 4b, 5a, 5b; R1 = Fc (H), R2 = H (Fc), 6a, 6b, 7a, 7b). Alkyne addition occurs at sulfur atoms of two different chelating 1,2-dicarba-closo-dodecaborane-1,2-dithiolate ligands that leads to a change of 16e Ru(IV) in 1a and 1b to 18e Ru(II) in 2a−7a and 2b−7b, respectively. Moreover, the reaction of 1a with ethynylferrocene produces an unprecedented tetranuclear mixed-valent Ru(IV)Ru(II)3S12 cluster (8a) consisting of two 1a and one ethynylferrocene through the cleavage and generation of Ru−S, S−S, and C−S bonds. The complexes were characterized by IR, MS, and NMR spectroscopy and microanalysis. X-ray structural analyses were performed on 1b, 2a, 3b, 5a, 5b, 7b, and 8a.
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