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The surface chemistry of isolated and aggregated silica-bound rhodium complexes

Journal Article · · Journal of Catalysis; (USA)

The chemisorption activity of silica-bound molecular Rh complexes has been studied using Fourier transform infrared, temperature-programmed desorption, and X-ray photoelectron spectroscopy on samples treated variously with CO, NO, and H{sub 2}. Beginning with a {mu}-oxo rhodium carbonyl species, treatment with NO leads to no (bis)nitrosyl rhodium complexes but to a mixture of an oxygen adduct and a nitrite/nitrate complex. Treatment of the latter with CO does not form isocyanate; treatment of it with H{sub 2} leads to an aggregated Rh complex and an unidentified complex, probably involving nitrogen and derived from the nitrate/nitrite complex. Treatment of the aggregated complex with NO and CO leads to some isocyanate on the Rh but none on the support. High-temperature treatment under vacuum leads to irreversible sintering after which the Rh behaves like conventional Rh metal particles with respect to formation of isocyanate on both the metal and the support upon exposure to NO and CO. The authors conclude that isocyanate formation depends strongly on the form of the Rh.

OSTI ID:
7055418
Journal Information:
Journal of Catalysis; (USA), Journal Name: Journal of Catalysis; (USA) Vol. 120:2; ISSN 0021-9517; ISSN JCTLA
Country of Publication:
United States
Language:
English

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