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gamma-Al(2)O(3)-supported Ir(4) and Ir(6) were prepared by decarbonylation of tetra- and hexanuclear iridium carbonyls, respectively, and compared as catalysts for ethene hydrogenation at atmospheric pressure and temperatures in the range 273-300 K. Rates of the reaction were determined along with extended X-ray absorption fine structure (EXAFS) and IR spectra characterizing the clusters in the working catalysts. EXAFS data show that the Ir(4) and Ir(6) cluster frames remained intact during catalysis. Di-sigma-bonded ethene and pi-bonded ethene on the clusters were identified by IR spectroscopy and found to compete as the principal reaction intermediates, with the former predominating at ethene partial pressures less than about 200 Torr and the latter at higher ethene partial pressures. Hydrogen on the clusters is inferred to form by dissociative adsorption of H(2); alternatively, it is provided by OH groups of the support. The rate of ethene hydrogenation on Ir(4) is typically several times greater than that on Ir(6).
Argo et al. (Sat,) studied this question.