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Título: | Chiral imprinting with amino acids of ordered mesoporous silica exhibiting enantioselectivity after calcination |
Autor: | Romero, Pilar CSIC ORCID ; Larrea, A. CSIC ORCID ; Vispe, Eugenio CSIC ORCID; López-Ram-de-Víu, Pilar CSIC ORCID ; Uriel, Santiago CSIC ORCID; Coronas, Joaquín CSIC ORCID | Fecha de publicación: | 2011 | Editor: | American Chemical Society | Citación: | Chemistry of Materials 23(5): 1280-1287 (2011) | Resumen: | Chiral ordered mesoporous silica (COMS) was synthesized in basic media by combining tetraethyl orthosilicate and quaternized aminosilane (with a templating role) silica sources together with four different standard amino acids (arginine, histidine, isoleucine, and proline). Besides the hexagonal MCM-41-type structure, narrow pore size distribution, and high specific surface area, it was found that these solids have potential for enantiomeric separation because of the transference of chirality from the amino acid to the silica. This is illustrated by the resolution of several racemic mixtures (those of proline, isoleucine, trans-4-hydroxyproline, pipecolic acid, valine, leucine, and phenylglycine) with the calcined COMS prepared with l-proline. The opposite behavior observed in induced circular dichroism experiments with calcined COMS, obtained using both enantiomers of proline, confirmed their chiral nature. The high number and variety of existing amino acids, and chiral organic compounds in general, makes these ordered silicas attractive for the production of enantiopure substances.(Figure Presented) © 2011 American Chemical Society. | URI: | http://hdl.handle.net/10261/52493 | DOI: | 10.1021/cm1032546 | Identificadores: | doi: 10.1021/cm1032546 issn: 0897-4756 e-issn: 1520-5002 |
Aparece en las colecciones: | (ICMA) Artículos |
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