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Artículo

Supramolecular Assemblies Obtained by Mixing Different Cyclodextrins and AOT or BHDC Reverse Micelles

Silva, Oscar FernandoIcon ; Correa, Nestor MarianoIcon ; Chessa, Juana JosefaIcon ; Hoyos, Maria Rita MicaelaIcon ; Fernández, Mariana AdelaIcon
Fecha de publicación: 03/2014
Editorial: American Chemical Society
Revista: Langmuir
ISSN: 0743-7463
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Otras Ciencias Químicas

Resumen

In this contribution we show the effect of the surfactant polar head and the external solvent on the incorporation of different cyclodextrins (CDs) {α-CD, β-CD, γ-CD, decenylsuccinyl-β-CD (Mod-β-CD), and hydroxypropyl-β-CD (hp-β-CD)} in different reverse micelles (RMs) {benzene/sodium 1,4-bis(2-ethylhexyl) sulfosuccinate(AOT)/water, and benzene/benzyl-n-hexadecyldimethylammonium chloride (BHDC)/water} and compare them with previous results obtained in n-heptane/AOT/water RMs. To investigate the different systems, we have used UV–vis spectrophotometry, induced circular dichroism spectroscopy (ICD), and the achiral molecular probe methyl orange (MO). The results show dramatic differences changing the external solvent and the surfactant, which are explained by considering the differences in the RMs interface composition, the water–surfactant interaction, and the CDs’ location in the different media investigated. None of the CDs were incorporated into the benzene/AOT/water RMs at any [H2O]/[surfactant] ratio studied (W0) whereas it was previously shown that Mod-β-CD and hp-β-CD could be included in n-heptane/AOT/water RMs. However, all of the CDs are incorporated in benzene/BHDC/water RMs at W0 > 10 and hp-β-CD is dissolved even at W0 = 0. Different from what was found in n-heptane/AOT RMs, in BHDC RMs MO showed ICD signals with two different CDs: Mod-β-CD and hp-β-CD. The results are explained by considering the known difference in the interfacial water structure for AOT and BHDC RMs and the electron-rich region on the secondary hydroxyl (wider side of the CDs), which helps to solubilize all CDs in BHDC. This study shows that chiral cyclodextrin could be available for a guest in an organic medium such as the RMs. Therefore we have created a potentially powerful nanoreactor with two different confined regions in the same aggregate: the polar core of the RMs and the chiral hydrophobic cavity of cyclodextrin.
Palabras clave: Cycilodextrins , Reverse Micelle , Chiral Complex , Dichroism Circular Induced
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info:eu-repo/semantics/openAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/31570
DOI: http://dx.doi.org/10.1021/la404584q
URL: http://pubs.acs.org/doi/10.1021/la404584q
Colecciones
Articulos(CCT - CORDOBA)
Articulos de CTRO.CIENTIFICO TECNOL.CONICET - CORDOBA
Articulos(INFIQC)
Articulos de INST.DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Citación
Silva, Oscar Fernando; Correa, Nestor Mariano; Chessa, Juana Josefa; Hoyos, Maria Rita Micaela; Fernández, Mariana Adela; Supramolecular Assemblies Obtained by Mixing Different Cyclodextrins and AOT or BHDC Reverse Micelles; American Chemical Society; Langmuir; 30; 12; 3-2014; 3354-3362
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