Abstract

Alumina-supported catalysts were prepared by conventional aqueous impregnation with [H 2OsCl 6] and by reaction of organoosmium clusters {[Os 3(CO) 12], [H 4Os 4(CO) 12], and [Os 6(CO) 18]} with the support. The catalysts were tested for CO hydrogenation at 250–325 °C and 10 atm, the products being Schulz-Flory distributions of hydrocarbons with small yields of dimethyl ether. The fresh and used catalysts were characterized by infrared spectroscopy and high-resolution transmission electron microscopy. The catalyst prepared from [H 2OsCl 6] had larger particles of Os (~70 Å). The cluster-derived catalysts initially consisted of molecular clusters on the support; the used catalysts contained small Os aggregates (typically 10–20 Å in diameter). The catalytic activity for hydrocarbon formation increased with increasing Os aggregate size, but the activity for dimethyl ether formation was almost independent of aggregate size. The hydrocarbon synthesis was evidently catalyzed by the Os aggregates, and the ether synthesis was perhaps catalyzed by mononuclear Os Complexes.

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