Abstract
Oxovanadium(IV) and dioxomolybdenum(VI) salen complexes were firstly tethered onto amino-functionalized mesoporous SBA-15 materials by a stepwise procedure and were screened as catalysts for the epoxidation of cyclooctene. The mesoporous structural integrity throughout the tethering procedure, the successful tethering of the organometallic complexes, the loadings of metal ions and organic ligands as well as the catalyst surface constitution and location of active organometallic species on the SBA-15 support were determined by comprehensive characterization techniques such as XRD, N 2 adsorption/desorption, FT-IR, UV–vis spectroscopy, ICP-AES, XPS and TG/DTA. Catalytic properties in the epoxidation of cyclooctene demonstrate that both tethered oxovanadium(IV) and dioxomolybdenum(VI) catalysts were more active than their respective homogeneous analogue, and the tethered oxovanadium(IV) complex showed the best activity (64.3%) with H 2O 2 as the oxidant and CH 3CN as the solvent.
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