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
- 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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1842269944908087296 |
score |
13.13397 |