The mesoporous molecular sieve MCM-41 was covalently grafted with 3-chloropropyl trimethoxylsilane and then was reacted with [Cr(salpr)(H2O)]Cl, (salpr = N,N'-bis(3-salicylidenaminopropyl)amine) to afford MCM-41 containing Cr(salpr) moiety, Cr(salpr)MCM-41. Powder X-ray diffraction and nitrogen adsorption-desorption analyses revealed that not only the textural characteristics of the support were preserved during the grafting experiments but also the channels remained accessible despite sequential reduction in surface area, pore volume and pore size. The chromium content of the prepared catalyst was 0.57 mmol.g-1. The chromium-containing MCM-41 was shown to successfully catalyze the epoxidation of 1-hexene, 1-octene, cyclohexene, cyclooctene, trans-stilbene and norbornene and also benzylic oxidation of toluene and ethyl benzene with tert-butylhydroperoxide (TBHP).
Masteri-Farahani,M . (2012). Synthesis, Characterization and Catalytic Activity of a New Chromium Catalyst Supported on Nanoporous MCM-41 for Oxidation of Olefins and Alkyl Aromatics. Journal of Sciences, Islamic Republic of Iran, 23(3), 219-223.
MLA
Masteri-Farahani,M . "Synthesis, Characterization and Catalytic Activity of a New Chromium Catalyst Supported on Nanoporous MCM-41 for Oxidation of Olefins and Alkyl Aromatics", Journal of Sciences, Islamic Republic of Iran, 23, 3, 2012, 219-223.
HARVARD
Masteri-Farahani M. (2012). 'Synthesis, Characterization and Catalytic Activity of a New Chromium Catalyst Supported on Nanoporous MCM-41 for Oxidation of Olefins and Alkyl Aromatics', Journal of Sciences, Islamic Republic of Iran, 23(3), pp. 219-223.
CHICAGO
M Masteri-Farahani, "Synthesis, Characterization and Catalytic Activity of a New Chromium Catalyst Supported on Nanoporous MCM-41 for Oxidation of Olefins and Alkyl Aromatics," Journal of Sciences, Islamic Republic of Iran, 23 3 (2012): 219-223,
VANCOUVER
Masteri-Farahani M. Synthesis, Characterization and Catalytic Activity of a New Chromium Catalyst Supported on Nanoporous MCM-41 for Oxidation of Olefins and Alkyl Aromatics. J. Sci. I. R. I.. 2012;23(3):219-223.