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dc.contributor.author
Silva, Oscar Fernando

dc.contributor.author
Correa, Nestor Mariano

dc.contributor.author
Chessa, Juana Josefa

dc.contributor.author
Hoyos, Maria Rita Micaela

dc.contributor.author
Fernández, Mariana Adela

dc.date.available
2017-12-26T19:02:57Z
dc.date.issued
2014-03
dc.identifier.citation
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
dc.identifier.issn
0743-7463
dc.identifier.uri
http://hdl.handle.net/11336/31570
dc.description.abstract
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.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society

dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Cycilodextrins
dc.subject
Reverse Micelle
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Chiral Complex
dc.subject
Dichroism Circular Induced
dc.subject.classification
Otras Ciencias Químicas

dc.subject.classification
Ciencias Químicas

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CIENCIAS NATURALES Y EXACTAS

dc.title
Supramolecular Assemblies Obtained by Mixing Different Cyclodextrins and AOT or BHDC Reverse Micelles
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2017-12-26T14:31:51Z
dc.journal.volume
30
dc.journal.number
12
dc.journal.pagination
3354-3362
dc.journal.pais
Estados Unidos

dc.journal.ciudad
Washington
dc.description.fil
Fil: Silva, Oscar Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.description.fil
Fil: Correa, Nestor Mariano. Universidad Nacional de Río Cuarto; Argentina
dc.description.fil
Fil: Chessa, Juana Josefa. Universidad Nacional de Río Cuarto; Argentina
dc.description.fil
Fil: Hoyos, Maria Rita Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.description.fil
Fil: Fernández, Mariana Adela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.journal.title
Langmuir

dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/la404584q
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/la404584q
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