Dissociation of acetaldehyde on beta-Mo2C to yield ethylidene and oxo surface groups: a possible pathway for active site formation in heterogeneous olefin metathesis.

Abstract

The dissociative adsorption of acetaldehyde on beta-Mo2C was studied using reflection absorption infrared spectroscopy. In contrast to what is observed for all metals previously studied, acetaldehyde undergoes selective carbonyl bond scission on the carbide surface. By comparison to calculated spectra, the surface product is identified as an oxo-ethylidene species. The study thus provides the first extended-range infrared spectrum of a propene metathesis initiator or propagator alkylidene. Aldehydes may be formed in the presence of olefins during the induction period of supported metal oxide olefin metathesis catalysts. Hence, the observed dissociative chemisorption of acetaldehyde suggests a possible answer to the question of how initiator sites are formed in heterogeneous olefin metathesis. This question has never been satisfactorily answered. In the proposed mechanism, aldehydes formed during the induction period subsequently react with the catalyst surface to generate alkylidene sites.