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Título: | Self-assembly of chiral (1R,2S)-ephedrine and (1S,2S)-pseudoephedrine into low-dimensional aluminophosphate materials driven by their amphiphilic nature |
Autor: | Bernardo-Maestro, Beatriz CSIC; Garrido-Martín, Elisa; López-Arbeloa, Fernando; Pérez-Pariente, Joaquín CSIC ORCID ; Gómez-Hortigüela Sainz, Luis CSIC ORCID | Palabras clave: | Aluminophosphates Ephedrine Pseudoephedrine Supramolecular Self-assembly Chirality |
Fecha de publicación: | 15-mar-2018 | Editor: | Royal Society of Chemistry (UK) | Citación: | Physical Chemistry Chemical Physics13: 8564-8578 (2018) | Resumen: | In an attempt to promote the crystallization of chiral inorganic frameworks, we explore the ability of chiral (1R,2S)-ephedrine and its diastereoisomer (1S,2S)-pseudoephedrine to act as organic building blocks for the crystallization of hybrid organo-inorganic aluminophosphate frameworks in the presence of fluoride. These molecules were selected because of their particular molecular asymmetric structure, which enables a rich supramolecular chemistry and a potential chiral recognition phenomenon during crystallization. Up to four new low-dimensional materials have been produced, wherein the organic molecules form an organic bilayer in-between the inorganic networks. We analyze by molecular simulations the trend of these chiral molecules to form these types of framework, which is directly related to their amphiphilic nature that triggers a strong self-assembly through hydrophobic interactions between aromatic rings and hydrophilic interactions with the fluoro-aluminophosphate inorganic units. Such a self-assembly process is strongly dependent on the concentration of the organic molecules. | Versión del editor: | http://dx.doi.org/10.1039/c7cp08573g | URI: | http://hdl.handle.net/10261/162386 | DOI: | 10.1039/c7cp08573g | ISSN: | 1463-9076 | E-ISSN: | 1463-9084 |
Aparece en las colecciones: | (ICP) Artículos |
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amphiphilic_nature.pdf | 4,04 MB | Adobe PDF | Visualizar/Abrir |
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