Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media

Autores
Pellegrino Vidal, Rocio; Ibañez, Gabriela Alejandra; Escandar, Graciela Monica
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
This study focuses on the spectrofluorimetric behavior of bisphenol A (BPA), 4-octylphenol (OP) and 4-nonylphenol (NP) in the presence of native and derivative cyclodextrins (CDs). The weak fluorescence emission bands of these endocrine disrupting compounds in aqueous media are significantly enhanced by β-CD and its hydroxyethyl-, hydropropyl, methyl-, and heptakis(2,6-di-o-methyl)-derivatives. A 1 : 1 guest : host stoichiometry for most complexes is established, although the additional presence of weak 1 : 2 complexes is suggested in both BPA–hydroxyethyl–β-CD and BPA–heptakis(2,6-di-o-methyl)–β-CD systems. The association constants are calculated by applying a non-linear regression method to the changes brought about by the presence of each CD in the corresponding fluorescence spectra, and these values are corroborated using a Benesi–Hildebrand type equation. The participation of the CD substituents in the inclusion phenomenon is indirectly demonstrated through the comparison of the acidity constant values in the absence and in the presence of β-CD derivatives. On the basis of 1H-NMR studies, possible structures of the formed complexes are suggested, and the structural information is supplemented by AM1 semiempirical calculations. The potential of the studied complexes in relation to their use for analytical purposes and/or for environmental remediation is discussed.
Fil: Pellegrino Vidal, Rocio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Ibañez, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Escandar, Graciela Monica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Materia
Cyclodextrin
Phenols
Fluorescence
Endocrine Disruptors
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/6128

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spelling Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins mediaPellegrino Vidal, RocioIbañez, Gabriela AlejandraEscandar, Graciela MonicaCyclodextrinPhenolsFluorescenceEndocrine Disruptorshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1This study focuses on the spectrofluorimetric behavior of bisphenol A (BPA), 4-octylphenol (OP) and 4-nonylphenol (NP) in the presence of native and derivative cyclodextrins (CDs). The weak fluorescence emission bands of these endocrine disrupting compounds in aqueous media are significantly enhanced by β-CD and its hydroxyethyl-, hydropropyl, methyl-, and heptakis(2,6-di-o-methyl)-derivatives. A 1 : 1 guest : host stoichiometry for most complexes is established, although the additional presence of weak 1 : 2 complexes is suggested in both BPA–hydroxyethyl–β-CD and BPA–heptakis(2,6-di-o-methyl)–β-CD systems. The association constants are calculated by applying a non-linear regression method to the changes brought about by the presence of each CD in the corresponding fluorescence spectra, and these values are corroborated using a Benesi–Hildebrand type equation. The participation of the CD substituents in the inclusion phenomenon is indirectly demonstrated through the comparison of the acidity constant values in the absence and in the presence of β-CD derivatives. On the basis of 1H-NMR studies, possible structures of the formed complexes are suggested, and the structural information is supplemented by AM1 semiempirical calculations. The potential of the studied complexes in relation to their use for analytical purposes and/or for environmental remediation is discussed.Fil: Pellegrino Vidal, Rocio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaFil: Ibañez, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaFil: Escandar, Graciela Monica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaRoyal Society of Chemistry2015-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/6128Pellegrino Vidal, Rocio; Ibañez, Gabriela Alejandra; Escandar, Graciela Monica; Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media; Royal Society of Chemistry; RSC Advances; 5; 27; 2-2015; 20914-209232046-2069enginfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2015/RA/c4ra13023einfo:eu-repo/semantics/altIdentifier/doi/10.1039/C4RA13023Einfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:06:09Zoai:ri.conicet.gov.ar:11336/6128instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:06:10.153CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
title Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
spellingShingle Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
Pellegrino Vidal, Rocio
Cyclodextrin
Phenols
Fluorescence
Endocrine Disruptors
title_short Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
title_full Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
title_fullStr Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
title_full_unstemmed Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
title_sort Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media
dc.creator.none.fl_str_mv Pellegrino Vidal, Rocio
Ibañez, Gabriela Alejandra
Escandar, Graciela Monica
author Pellegrino Vidal, Rocio
author_facet Pellegrino Vidal, Rocio
Ibañez, Gabriela Alejandra
Escandar, Graciela Monica
author_role author
author2 Ibañez, Gabriela Alejandra
Escandar, Graciela Monica
author2_role author
author
dc.subject.none.fl_str_mv Cyclodextrin
Phenols
Fluorescence
Endocrine Disruptors
topic Cyclodextrin
Phenols
Fluorescence
Endocrine Disruptors
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv This study focuses on the spectrofluorimetric behavior of bisphenol A (BPA), 4-octylphenol (OP) and 4-nonylphenol (NP) in the presence of native and derivative cyclodextrins (CDs). The weak fluorescence emission bands of these endocrine disrupting compounds in aqueous media are significantly enhanced by β-CD and its hydroxyethyl-, hydropropyl, methyl-, and heptakis(2,6-di-o-methyl)-derivatives. A 1 : 1 guest : host stoichiometry for most complexes is established, although the additional presence of weak 1 : 2 complexes is suggested in both BPA–hydroxyethyl–β-CD and BPA–heptakis(2,6-di-o-methyl)–β-CD systems. The association constants are calculated by applying a non-linear regression method to the changes brought about by the presence of each CD in the corresponding fluorescence spectra, and these values are corroborated using a Benesi–Hildebrand type equation. The participation of the CD substituents in the inclusion phenomenon is indirectly demonstrated through the comparison of the acidity constant values in the absence and in the presence of β-CD derivatives. On the basis of 1H-NMR studies, possible structures of the formed complexes are suggested, and the structural information is supplemented by AM1 semiempirical calculations. The potential of the studied complexes in relation to their use for analytical purposes and/or for environmental remediation is discussed.
Fil: Pellegrino Vidal, Rocio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Ibañez, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Escandar, Graciela Monica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
description This study focuses on the spectrofluorimetric behavior of bisphenol A (BPA), 4-octylphenol (OP) and 4-nonylphenol (NP) in the presence of native and derivative cyclodextrins (CDs). The weak fluorescence emission bands of these endocrine disrupting compounds in aqueous media are significantly enhanced by β-CD and its hydroxyethyl-, hydropropyl, methyl-, and heptakis(2,6-di-o-methyl)-derivatives. A 1 : 1 guest : host stoichiometry for most complexes is established, although the additional presence of weak 1 : 2 complexes is suggested in both BPA–hydroxyethyl–β-CD and BPA–heptakis(2,6-di-o-methyl)–β-CD systems. The association constants are calculated by applying a non-linear regression method to the changes brought about by the presence of each CD in the corresponding fluorescence spectra, and these values are corroborated using a Benesi–Hildebrand type equation. The participation of the CD substituents in the inclusion phenomenon is indirectly demonstrated through the comparison of the acidity constant values in the absence and in the presence of β-CD derivatives. On the basis of 1H-NMR studies, possible structures of the formed complexes are suggested, and the structural information is supplemented by AM1 semiempirical calculations. The potential of the studied complexes in relation to their use for analytical purposes and/or for environmental remediation is discussed.
publishDate 2015
dc.date.none.fl_str_mv 2015-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/6128
Pellegrino Vidal, Rocio; Ibañez, Gabriela Alejandra; Escandar, Graciela Monica; Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media; Royal Society of Chemistry; RSC Advances; 5; 27; 2-2015; 20914-20923
2046-2069
url http://hdl.handle.net/11336/6128
identifier_str_mv Pellegrino Vidal, Rocio; Ibañez, Gabriela Alejandra; Escandar, Graciela Monica; Spectrofluorimetric study of phenolic endocrine disruptors in cyclodextrins media; Royal Society of Chemistry; RSC Advances; 5; 27; 2-2015; 20914-20923
2046-2069
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2015/RA/c4ra13023e
info:eu-repo/semantics/altIdentifier/doi/10.1039/C4RA13023E
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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