“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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Published in | The journal of physical chemistry. B Vol. 107; no. 4; pp. 920 - 925 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
30.01.2003
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Online Access | Get full text |
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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. |
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Bibliography: | istex:D910803335662C294FDDA2D2F1725F7967DBCEA9 ark:/67375/TPS-05ZS7MW5-0 |
ISSN: | 1520-6106 1520-5207 |
DOI: | 10.1021/jp0205113 |