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Amine-Modified Silica NH2-(CH2)x-SiO2 (x = 0, 2, 3) as Support for Cobalt-Substituted Polyoxometalate TBA4HPW11CoO39: Effect of the Nature of the Support on the Oxidation Activity Full article

Journal Journal of Molecular Catalysis A: Chemical
ISSN: 1381-1169
Output data Year: 2010, Volume: 319, Number: 1-2, Pages: 119-125 Pages count : 7 DOI: 10.1016/j.molcata.2009.12.010
Tags Amino-groups, Immobilization, Oxidation, Polyoxometalates
Authors Panchenko V.N. 1 , Borbáth I. 2 , Timofeeva M.N. 1 , Gőbölös S. 2
Affiliations
1 Boreskov Institute of Catalysis SB RAS
2 Institute of Nanochemistry and Catalysis, Chemical Research Center, Hungarian Academy of Sciences

Funding (1)

1 National Research, Development and Innovation Office HAS-RAS/2008-2010 (No. 32)

Abstract: Acidic tetra-n-butylammonium (TBA) salts of Keggin type transition-metal-monosubstituted polyoxometalate TBA4HPW11CoO39 (Co-POM) have been chemically anchored to the amino-modified silica (NH2–(CH2)x–SiO2, x = 0, 2, 3) containing 40–710 μmol NH2-groups per 1 g of support. The interaction of Co-POM with NH2–(CH2)x–SiO2 was studied by DR-UV–vis spectroscopy. Spectroscopic data revealed that the type of interaction between Co-POM and support depends on the amount of anchored functional NH2-groups. It was found that Co-POM was attached to NH2–(CH2)x–SiO2 support both by the electrostatic NH3+⋯Co-POM− and dative (Si–OH⋯Co-POM) bonding. Both the amount of anchored NH2-groups and the distance between NH2-group and surface of silica affect the nature of the interaction between Co-POM and surface functional groups. The increase of the amount of anchored NH2–(CH2)3-groups leads to decrease in the contribution of dative bonding Si–OH⋯Co-POM and an increase in the contribution of electrostatic bonding NH3+⋯Co-POM−. The activity of the immobilized Co-POM was tested in benzyl alcohol oxidation with oxygen in CH3CN medium. It was found that catalytic activity and stability of Co-POM depend on the nature of interaction between Co-POM and surface groups of support that is adjustable both by the amount of anchored functional NH2-groups on silica support and the distance between NH2-group and surface of silica.
Cite: Panchenko V.N. , Borbáth I. , Timofeeva M.N. , Gőbölös S.
Amine-Modified Silica NH2-(CH2)x-SiO2 (x = 0, 2, 3) as Support for Cobalt-Substituted Polyoxometalate TBA4HPW11CoO39: Effect of the Nature of the Support on the Oxidation Activity
Journal of Molecular Catalysis A: Chemical. 2010. V.319. N1-2. P.119-125. DOI: 10.1016/j.molcata.2009.12.010 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jun 27, 2009
Accepted: Dec 21, 2009
Published online: Dec 29, 2009
Published print: Mar 17, 2010
Identifiers:
Web of science: WOS:000275244800015
Scopus: 2-s2.0-75149115649
Elibrary: 15315032
Chemical Abstracts: 2010:134841
Chemical Abstracts (print): 152:571042
OpenAlex: W2080649912
Citing:
DB Citing
Web of science 31
Scopus 34
Elibrary 33
OpenAlex 31
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