Reaction of the sodium metalates Na[M(CO)2C5R5] [M = Fe, R = H (1a), Me (1b); M = Ru, R = H (1c), Me (1d)] with an equimolar amount of hexachlorodisilane yields the metallo‐pentachlorodisilanes C5R5(OC)2M–SiCl2–SiCl3 (2a–d), which can be converted into the pentahydrido analogues C5R5(OC)2M–SiH2–SiH3 (3a–c) via Cl/H exchange with LiAlH4. Due to the activating effect of the transition metal fragment chlorination of 3a–c with CCl4 or HCCl3 occurs at the α‐silicon to give C5R5(OC)2M–SiCl2–SiH3 (4a–c). The metallo‐disilanes were characterised by 1H‐, 13C‐, 29Si‐NMR, IR and especially Raman spectroscopy. The structures of C5H5(OC)2Fe–Si2Cl5 (2a) andC5Me5(OC)2Fe–Si2H5 (3b) have been determined by X‐ray analysis; 2a,b, 3a,b were theoretically described by DFT calculations.