The mixed-metal complex, [RhOs(CO)(4)(dppm)(2)][BF4] (1; dppm = gamma-Ph2PCH2PPh2) reacts with diazomethane to yield a number of products resulting from methylene incorporation into the bimetallic core. At -80degreesC the reaction between 1 and CH2N2 yields the methylene-bridged [RhOs(CO)(3)(mu-CH2)(mu-CO)-(dppm)(2)][BF4] (2), which reacts further at ambient temperature to give the allyl methyl species, [RhOs(eta(1)-C3H5)(CH3)(CO)(3)(dppm)(2)][BF4] (4). At intermediate temperatures Compounds 1 and 2 react with diazomethane to yield the butanediyl complex [RhOs(C4H8)(CO)(3)(dppm)(2)][BF4] (3) by the incorporation and coupling of four methylene units. Compound 2 is proposed to be an intermediate in the formation of 3 and 4 from 1 and on the basis of labeling studies a mechanism has been proposed in which sequential insertions of diazomethane-generated methylene fragments into the Rh-C bond of bridging hydrocarbyl fragments occur. Reaction of the tricarbonyl species, [RhOs(CO)(3)(mu-CH2)(dppm)(2)][BF4] with diazomethane over a range of temperatures generates the ethylene complex [RhOs(eta(2)-C2H4)(CO)(3)(dppm)(2)][BF4] (7a), but no further incorporation of methylene groups is observed. This observation suggests that carbonyl loss in the formation of the above allyl and butanediyl species only occurs after incorporation of the third methylene fragment. Attempts to generate C-2-bridged species by the reaction of 1 with ethylene gave no reaction, however, in the presence of trimethylamine oxide the ethylene adducts [RhOS(eta(2)-C2H4)(CO)(3)(dppm)(2)][BF4] (7b; an isomer of 7a) and [RhOs(eta(2)-C2H4)(2)(CO)(2)(dppm)(2)][BF4] (8) were obtained. The relationship of the above products to the selective coupling of methylene groups, and the roles of the different metals are discussed.