Chiral ruthenium porphyrin encapsulated in ordered mesoporous molecular sieves (MCM-41 and MCM-48) as catalysts for asymmetric alkene epoxidation and cyclopropanationElectronic supplementary information (ESI) available: experimental section. See http://www.rsc.org/suppdata/cc/b2/b209276j/

2002 ◽  
pp. 2906-2907 ◽  
Author(s):  
Jun-Long Zhang ◽  
Yun-Ling Liu ◽  
Chi-Ming Che
Author(s):  
Marcela N. Barbosa ◽  
Maria J. F. Costa ◽  
Maricele N. Barbosa ◽  
Valter J. Fernandes Jr. ◽  
Giancarlo R. Salazar-Banda ◽  
...  

The adsorption of carbon dioxide on amino silanes-functionalized MCM-41 and SBA-15 materials is reported. The functionalization of mesoporous silicas was made by post-synthesis method, by impregnation of 3-aminopropyltriethoxysilane. The obtained materials were characterized by X-ray diffraction, scanning and transmission electron microscopies, nitrogen adsorption-desorption and X-ray photoelectron spectroscopy measurements. The carbon dioxide adsorption capacities for the samples were carried out under ambient pressures. The obtained results evidenced that amino-silanes with a terminal amine (–NH2) were functionalized through covalent coupling of this group on the surface of the channels in the ordered mesoporous silica, meaning that the amine is anchored on the surface of the bigger pores of the MCM-41 and SBA-15 support. For functionalized materials, the CO2 adsorption capacity of the AMCM-41 increased from 0.18 to 1.1 mmol·g−1, whereas for ASBA-15, it was from 0.6 to 1.8 mmol·g−1. The Lagergren kinetic algorithms were applied in order to validate the obtained results, evidencing the enhanced carbon dioxide adsorption capacity and stability of the functionalized ordered mesoporous molecular sieves.


1999 ◽  
Vol 2 (3) ◽  
pp. 173-179 ◽  
Author(s):  
Rogério A.A. Melo ◽  
Marcus V. Giotto ◽  
João Rocha ◽  
Ernesto A. Urquieta-González

Author(s):  
Marcela N. Barbosa ◽  
Maria J. F. Costa ◽  
Maricele N. Barbosa ◽  
Valter J. Fernandes Jr. ◽  
Giancarlo R. Salazar-Banda ◽  
...  

The adsorption of carbon dioxide on amino silanes-functionalized MCM-41 and SBA-15 materiais is reported. The functionalization of mesoporous silicas was made by post-synthesis method, by impregnation of 3-aminopropyltriethoxysilane. The obtained materials were characterized by X-ray diffraction, scanning and transmission electron microscopies, nitrogen adsorption-desorption and X-ray photoelectron spectroscopy measurements. The carbon dioxide adsorption capacities for the samples were carried out under ambient pressures. The obtained results evidenced that amino-silanes with a terminal amine (–NH2) were functionalized through covalent coupling of this group on the surface of the channels in the ordered mesoporous silica, meaning that the amine is anchored on the surface of the bigger pores of the MCM-41 and SBA-15 support. For functionalized materials, the CO2 adsorption capacity of the AMCM-41 increased from 0.18 to 1.1 mmol g−1, whereas for ASBA-15, it was from 0.6 to 1.8 mmol g−1. The Lagergren kinetic algorithms were applied in order to validate the obtained results, evidencing the enhanced carbon dioxide adsorption capacity and stability of the functionalized ordered mesoporous molecular sieves.


1999 ◽  
Vol 35 (1) ◽  
pp. 52-56
Author(s):  
F. M. Bobonich ◽  
Yu. G. Voloshina ◽  
L. A. Matkovskaya ◽  
V. N. Solomakha ◽  
Yu. G. Gol’tsov

2011 ◽  
Vol 7 ◽  
pp. 22-28 ◽  
Author(s):  
Hynek Balcar ◽  
Tushar Shinde ◽  
Naděžda Žilková ◽  
Zdeněk Bastl

A commercially available Hoveyda–Grubbs type catalyst (RC303 Zhannan Pharma) was immobilized on mesoporous molecular sieves MCM-41 and on SBA-15 by direct interaction with the sieve wall surface. The immobilized catalysts exhibited high activity and nearly 100% selectivity in several types of alkene metathesis reactions. Ru leaching was found to depend on the substrate and solvent used (the lowest leaching was found for ring-closing metathesis of 1,7-octadiene in cyclohexane – 0.04% of catalyst Ru content). Results of XPS, UV–vis and NMR spectroscopy showed that at least 76% of the Ru content was bound to the support surface non-covalently and could be removed from the catalyst by washing with THF.


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