“Side Chain” Modification of MCM-41 Silica through the Exchange of the Surfactant Template with Charged Functionalized Organosiloxanes:  An Efficient Route to Valuable Reconstructed MCM-41 Derivatives

The synthesis of “side chain” functionalized MCM-41 inorganic−organic hybrids, through the exchange method of the template with the cationic organosiloxanes (CH3O)3SiCH2CH2CH2NH3 +Cl-, (CH3O)3SiCH2CH2CH2NHCH2CH2NH3 +Cl-, and (CH3CH2O)3SiCH2CH2CH2N(CH3)3 +Cl- is reported. The first two derivatives ar...

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Bibliographic Details
Published inThe journal of physical chemistry. B Vol. 107; no. 4; pp. 920 - 925
Main Authors Bourlinos, A. B, Karakostas, Th, Petridis, D
Format Journal Article
LanguageEnglish
Published American Chemical Society 30.01.2003
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Summary:The synthesis of “side chain” functionalized MCM-41 inorganic−organic hybrids, through the exchange method of the template with the cationic organosiloxanes (CH3O)3SiCH2CH2CH2NH3 +Cl-, (CH3O)3SiCH2CH2CH2NHCH2CH2NH3 +Cl-, and (CH3CH2O)3SiCH2CH2CH2N(CH3)3 +Cl- is reported. The first two derivatives are converted to free basis by neutralization of the acidic forms with Na2CO3. After the exchange and neutralization reactions, the as received derivatives retain the hexagonal symmetry of the original MCM-41 material, whereas, due to the high loading of the pore channels of the MCM-41 silica with the organo-modifier, the final solids exhibit rather small BET surface areas (∼100 m2 g-1) and microporosity. The functionalized organic moieties, covalently attached to the walls of the MCM-41 mesoporous silica, exhibit the characteristic reactions of the particular end groups, including nucleophilic substitution reactions, chelation of transition metal ions, and anion exchange behavior.
Bibliography:istex:D910803335662C294FDDA2D2F1725F7967DBCEA9
ark:/67375/TPS-05ZS7MW5-0
ISSN:1520-6106
1520-5207
DOI:10.1021/jp0205113