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Get Free AccessThe one-pot epoxidation of alkenes with O2 is performed with nano-particulated Au/CeO2 and Ti-MCM-41 silylated materials in the presence of a hydrocarbon and azobis-iso-butyronitrile (AIBN) as a promoter. This initiator is able to form organo-gold species that promote the formation of hydrocarbon (3-methyl-pentane, ethylbenzene, or cumene) hydroperoxides which in the presence of Ti-mesoporous material epoxidize the alkene in good yields. The epoxidation reaction of 1-octene with molecular oxygen ( P O 2 = 12 bars ) at 90°C over AIBN–Au/CeO2 +Ti-MCM-41-silylated catalytic system results in alkene conversions close to 9% (≈40% of the maximum conversion attainable) with epoxide selectivity around 90% when working with cumene as a sacrificial hydrocarbon.
Carmela Aprile, Avelino Avelino, Marcelo E. Domine, Hermenegildo Garcı́a, Chris J. Mitchell (2009). A cascade aerobic epoxidation of alkenes over Au/CeO2 and Ti-mesoporous material by “in situ” formed peroxides. Journal of Catalysis, 264(1), pp. 44-53, DOI: 10.1016/j.jcat.2009.03.010.
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Type
Article
Year
2009
Authors
5
Datasets
0
Total Files
0
Language
English
Journal
Journal of Catalysis
DOI
10.1016/j.jcat.2009.03.010
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