Abstract
The catalytic oxidation of cis-2-butene and propylene with molecular oxygen in the presence of a well-defined surface coordination compound, (≡SiO)2Mo(=O)2, affords acetaldehyde. Using a cis-2-butene/O2 feed at 350-400 °C, the reaction yields a conversion of approximately 10% and an acetaldehyde selectivity of approximately 70%. This performance is maintained up to an experimental time of 20 h in a continuous flow reactor. The Mo(bis-oxo) surface compound was fully characterized by multiple spectroscopic techniques as well as surface microanalysis. The results from quantum mechanics calculations indicate that the reaction proceeds via [2 + 2] cycloaddition/cycloelimination steps with the formation of metalla-oxacyclobutane intermediates, analogous to the Chauvin mechanism in olefin metathesis.
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CITATION STYLE
Le Quéméner, F., Barman, S., Merle, N., Aljuhani, M. A., Samantaray, M. K., Saih, Y., … Basset, J. M. (2018). Metathetic Oxidation of 2-Butenes to Acetaldehyde by Molecular Oxygen Using the Single-Site Olefin Metathesis Catalyst (≡SiO)2Mo(=O)2. ACS Catalysis, 8(8), 7549–7555. https://doi.org/10.1021/acscatal.8b01767
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