Solid state NMR characterisation of encapsulated molecules in mesoporous silica
Ibuprofen molecules have been encapsulated in mesoporous MCM-41 type-silica functionalised or not by amino groups. They have been characterised by 13C and 1H solid state NMR spectroscopy. The 13C MAS single pulse or cross polarization NMR spectra, as well as the 1H MAS NMR spectra demonstrate an ext...
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Veröffentlicht in: | Journal of sol-gel science and technology 2004-08, Vol.31 (1-3), p.219-223 |
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creator | BABONNEAU, Florence YEUNG, Laurence STEUNOU, Nathalie GERVAIS, Christel RAMILA, Ainhoa VALLET-REGI, Maria |
description | Ibuprofen molecules have been encapsulated in mesoporous MCM-41 type-silica functionalised or not by amino groups. They have been characterised by 13C and 1H solid state NMR spectroscopy. The 13C MAS single pulse or cross polarization NMR spectra, as well as the 1H MAS NMR spectra demonstrate an extremely high mobility of the ibuprofen molecules when the matrix is not functionalised. On the contrary, when the silica matrix is functionalized by amino groups, the 13C NMR response shows less mobility suggesting the existence of interactions between the amino groups and the carboxylic groups. Benzoic acid as well as benzamide have also been encapsulated and their NMR responses compared to that of ibuprofen. |
doi_str_mv | 10.1023/B:JSST.0000047991.73840.8b |
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They have been characterised by 13C and 1H solid state NMR spectroscopy. The 13C MAS single pulse or cross polarization NMR spectra, as well as the 1H MAS NMR spectra demonstrate an extremely high mobility of the ibuprofen molecules when the matrix is not functionalised. On the contrary, when the silica matrix is functionalized by amino groups, the 13C NMR response shows less mobility suggesting the existence of interactions between the amino groups and the carboxylic groups. Benzoic acid as well as benzamide have also been encapsulated and their NMR responses compared to that of ibuprofen.</description><identifier>ISSN: 0928-0707</identifier><identifier>EISSN: 1573-4846</identifier><identifier>DOI: 10.1023/B:JSST.0000047991.73840.8b</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Benzamide ; Benzoic acid ; Chemistry ; Colloidal gels. 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They have been characterised by 13C and 1H solid state NMR spectroscopy. The 13C MAS single pulse or cross polarization NMR spectra, as well as the 1H MAS NMR spectra demonstrate an extremely high mobility of the ibuprofen molecules when the matrix is not functionalised. On the contrary, when the silica matrix is functionalized by amino groups, the 13C NMR response shows less mobility suggesting the existence of interactions between the amino groups and the carboxylic groups. Benzoic acid as well as benzamide have also been encapsulated and their NMR responses compared to that of ibuprofen.</description><subject>Benzamide</subject><subject>Benzoic acid</subject><subject>Chemistry</subject><subject>Colloidal gels. Colloidal sols</subject><subject>Colloidal state and disperse state</subject><subject>Cross polarization</subject><subject>Encapsulation</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Ibuprofen</subject><subject>NMR spectroscopy</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Porous materials</subject><subject>Silicon dioxide</subject><subject>Solid state</subject><subject>Spectrum analysis</subject><issn>0928-0707</issn><issn>1573-4846</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpFkMtOwzAQRS0EEqXwDxaIZYodv7ujFU8VKtHuLddxhKs0Dnay4O9xaaXOZjZn7lwdAG4xmmBUkofZ9H21Wk_QfqhQCk8EkRRN5OYMjDATpKCS8nMwQqqUBRJIXIKrlLYZZxSLEViuQuMrmHrTO_j58QXtt4nG9i76ZHofWhhq6FprujQ0mangLjTODo1L0Ldw51LoQgxDgsk33pprcFGbJrmb4x6D9fPTev5aLJYvb_PHRWGJ4H3heC5HKSuNNIxLQhzN_bnChBtBczlSUVY7oTCvsOWEGcN5uakZsbhikozB3SG2i-FncKnX2zDENn_UZckUY0oglKnpgbIxpBRdrbvodyb-aoz03p-e6b0_ffKn__1pucnH98cXJlnT1NG01qdTAudIKFKSPyy0cJo</recordid><startdate>20040801</startdate><enddate>20040801</enddate><creator>BABONNEAU, Florence</creator><creator>YEUNG, Laurence</creator><creator>STEUNOU, Nathalie</creator><creator>GERVAIS, Christel</creator><creator>RAMILA, Ainhoa</creator><creator>VALLET-REGI, Maria</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>L6V</scope><scope>M7S</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope></search><sort><creationdate>20040801</creationdate><title>Solid state NMR characterisation of encapsulated molecules in mesoporous silica</title><author>BABONNEAU, Florence ; YEUNG, Laurence ; STEUNOU, Nathalie ; GERVAIS, Christel ; RAMILA, Ainhoa ; VALLET-REGI, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-e61574452a8a56833e404769136a740053d45fe7916d1c635aa662bf53c1d583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Benzamide</topic><topic>Benzoic acid</topic><topic>Chemistry</topic><topic>Colloidal gels. 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They have been characterised by 13C and 1H solid state NMR spectroscopy. The 13C MAS single pulse or cross polarization NMR spectra, as well as the 1H MAS NMR spectra demonstrate an extremely high mobility of the ibuprofen molecules when the matrix is not functionalised. On the contrary, when the silica matrix is functionalized by amino groups, the 13C NMR response shows less mobility suggesting the existence of interactions between the amino groups and the carboxylic groups. Benzoic acid as well as benzamide have also been encapsulated and their NMR responses compared to that of ibuprofen.</abstract><cop>Heidelberg</cop><pub>Springer</pub><doi>10.1023/B:JSST.0000047991.73840.8b</doi><tpages>5</tpages></addata></record> |
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subjects | Benzamide Benzoic acid Chemistry Colloidal gels. Colloidal sols Colloidal state and disperse state Cross polarization Encapsulation Exact sciences and technology General and physical chemistry Ibuprofen NMR spectroscopy Nonsteroidal anti-inflammatory drugs Porous materials Silicon dioxide Solid state Spectrum analysis |
title | Solid state NMR characterisation of encapsulated molecules in mesoporous silica |
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