“…As a result of the highly reversible orthometallation of [Os 3 (CO) 10 (μ-dppm)] ( 1 ) (dppm = Ph 2 PCH 2 PPh 2 ) to give the unsaturated cluster [Os 3 (CO) 8 {μ 3 -Ph 2 PCH 2 P(Ph)C 6 H 4 }(μ-H)] ( 2 ) with an accessible coordination site, the latter has proven to be a pivotal precursor for the synthesis of a wide variety of interesting and potentially useful clusters. Thus, 2 reacts with CO, H 2 , diphenylacetylene, [Au(PPh 3 )][PF 6 ], [Sn{CH(SiMe 3 ) 2 } 2 ], phosphines, thiols, organic-heterothiols, dithiols, diazomethane, PhSeSePh, HX (X = Cl, Br, F), and benzothiophene 27 under mild conditions. We recently reported the synthesis of the osmium−silicon clusters [Os 3 (CO) 9 (μ-dppm)(SiR 3 )(μ-H)] and [Os 3 (CO) 7 {μ 3 -Ph 2 PCH 2 P(Ph)C 6 H 4 }(SiR 3 )(μ-H) 2 ] (SiR 3 = SiPh 3 , SiEt 3 , SiEtMe 2 ) from the reaction of 2 with R 3 SiH and described the dynamic behavior of the former .…”