ISSN:
1572-9028
Keywords:
titania–silica aerogel
;
epoxidation
;
organic modification
;
methyltrimethoxysilane
;
phenyltrimethoxysilane
;
cyclohexene
;
cyclohexenol
;
tert-butylhydroperoxide
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract Titania–silica mixed oxides with covalently bound methyl or phenyl groups were prepared from the corresponding alkyltrimethoxysilane and tetramethoxysilane using a sol–gel process and ensuing low-temperature supercritical extraction with CO2. Prehydrolysis of the organically modified silicon precursor was applied to compensate for their lower sol–gel reactivity compared to the precursors of the other constituents. Trihexylamine was used as a gelation catalyst. The dominantly mesoporous aerogels were characterized by thermal analysis, N2 adsorption, infrared spectroscopy, 29Si- and 13C-NMR spectroscopy, and transmission electron microscopy. Thermal analysis and 29Si MAS NMR measurements indicated covalent incorporation of the modifying group. 13C NMR spectra confirmed the integrity of the incorporated modifying groups. The materials were tested in the epoxidation of cyclohexene and cyclohexenol with tert-butylhydroperoxide. NH3 adsorption studied by DRIFT spectroscopy indicated no significant acidity of the aerogel surfaces, which was traced to the use of trihexylamine as gelation catalyst. Addition of zeolite 4 Å or NaHCO3 did not improve the performance of the unmodified and phenyl-modified aerogel, corroborating the suppressed acidity of the surface. Interestingly, the phenyl-modified aerogel was more selective in the epoxidation of cyclohexenol, when using polar solvents (ethanol or acetone), compared to the reaction in toluene.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1023/A:1027202604286
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