Abstract
Ta-HMS mesoporous molecular sieve was synthesized hydrothermally and vapor-silylated using hexamethyldisilazane. Two samples were characterized by Fourier transform infrared spectrometry, 29Si cross-polarization and magic angle spinning nuclear magnetic resonance, hydrophilicity–lipophilicity tests, X-ray diffraction, N2 adsorption, and diffuse reflectance ultraviolet–visible spectroscopy (DR UV–Vis), respectively. They were also evaluated by the epoxidation of cyclohexene using tert-butyl hydroperoxide as oxidant. Trimethylsilyl groups have been anchored on the surface of Ta-HMS after silylation treatment. The silylated Ta-HMS keeps a typical mesoporous structure, whereas it has a less pore diameter and a less specific area than Ta-HMS. On the other hand, the silylated Ta-HMS gives the less hydrophilicity and higher lipophilicity as well as the higher dispersity of Ta sites than Ta-HMS, and as a result, the silylated Ta-HMS exhibits the more excellent catalytic performance in epoxidation of cyclohexene than Ta-HMS.
Graphical Abstract
Ta-HMS mesoporous molecular sieve was synthesized hydrothermally and vapor-silylated using hexamethyldisilazane. Trimethylsilyl groups have been anchored on the surface of Ta-HMS after silylation treatment. The silylated Ta-HMS keeps the typical mesoporous structure, whereas it has the less pore diameter and specific area compared with Ta-HMS. On the other hand, the silylated Ta-HMS gives the less hydrophilicity and higher lipophilicity as well as the higher dispersity of Ta sites than Ta-HMS, and as a result, the silylated Ta-HMS exhibits more excellent catalytic performance in epoxidation of cyclohexene than Ta-HMS.
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Acknowledgments
This work was supported by the Natural Science Foundation of Education Department of Henan Province in China (12B530004) and the Program for Young Core Teachers in Colleges and Universities of Henan Province in China (2012GGJS-171).
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Li, X. Vapor silylation of Ta-HMS mesoporous molecular sieve. J Sol-Gel Sci Technol 76, 476–481 (2015). https://doi.org/10.1007/s10971-015-3796-z
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DOI: https://doi.org/10.1007/s10971-015-3796-z