Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones

Autores
Pérez, María Emilia; Ruiz, Diego Manuel; Autino, Juan Carlos; Blanco, Mirta Noemí; Pizzio, Luis René; Romanelli, Gustavo Pablo
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Mesoporous TiO₂/H₃PW₁₂O₄₀ composites were synthesized by sol–gel reactions using urea as a low-cost template, and adding tungstophosphoric acid (TPA) at the same time as the template. The TPA concentration was varied in order to obtain TPA contents of 0, 10, and 20 (w/w) in the solid. The samples presented mesopores with a diameter higher than 3.0 nm. The specific surface area of the solids decreased with both the increase of the TPA content and the calcination temperature. From Fourier transform infrared and ³¹P magic angle spinning-nuclear magnetic resonance studies it was observed that the main heteropolyoxometallate species present in the composites is the [PW₁₂O₄₀]³⁻ anion, which was partially transformed into the [P₂W₂₁O₇₁]⁶⁻ and [PW₁₁O₃₉]⁷⁻ anions during the synthesis and drying step. The X-ray diffraction patterns of the modified samples only exhibited the characteristic peaks of the anatase phase of titanium oxide. The point of zero charge decreased with both the increase of TPA content in the solids and the calcination temperature. The materials were found to be efficient and recyclable catalysts for the synthesis of a series of flavones. The reaction was carried out in different reaction media: heterogeneous and solvent-free conditions. The solvent-free conditions represent the best green conditions. Initially, we optimize the reaction condition to obtain 6-chloroflavone by direct reaction of the cyclodehydration of 1-(2-hydroxy-5-chlorophenyl)-3-phenyl-1,3-propanodione in the presence of a catalytic amount of mesoporous titania modified with tungstophosphoric acid catalyst. Reactions were performed in two conditions: low volume of toluene, at 110 °C, typically 24 h, and solvent-free at the same temperature, 1 h. In all cases the product (6-chloroflavone) was obtained with high selectivity. Conversions up to 76 and 92 % were obtained respectively, using the supported catalyst (TiTPA10). Optimal reaction conditions were applied to the preparation of six substituted flavones in both conditions.
Facultad de Ciencias Agrarias y Forestales
Centro de Investigación y Desarrollo en Ciencias Aplicadas
Materia
Ciencias Exactas
Química
Mesoporous titania modified with tungstophosphoric
Keggin heteropolyacids
Flavone synthesis
Solvent-free organic reaction
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/139731

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oai_identifier_str oai:sedici.unlp.edu.ar:10915/139731
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavonesPérez, María EmiliaRuiz, Diego ManuelAutino, Juan CarlosBlanco, Mirta NoemíPizzio, Luis RenéRomanelli, Gustavo PabloCiencias ExactasQuímicaMesoporous titania modified with tungstophosphoricKeggin heteropolyacidsFlavone synthesisSolvent-free organic reactionMesoporous TiO₂/H₃PW₁₂O₄₀ composites were synthesized by sol–gel reactions using urea as a low-cost template, and adding tungstophosphoric acid (TPA) at the same time as the template. The TPA concentration was varied in order to obtain TPA contents of 0, 10, and 20 (w/w) in the solid. The samples presented mesopores with a diameter higher than 3.0 nm. The specific surface area of the solids decreased with both the increase of the TPA content and the calcination temperature. From Fourier transform infrared and ³¹P magic angle spinning-nuclear magnetic resonance studies it was observed that the main heteropolyoxometallate species present in the composites is the [PW₁₂O₄₀]³⁻ anion, which was partially transformed into the [P₂W₂₁O₇₁]⁶⁻ and [PW₁₁O₃₉]⁷⁻ anions during the synthesis and drying step. The X-ray diffraction patterns of the modified samples only exhibited the characteristic peaks of the anatase phase of titanium oxide. The point of zero charge decreased with both the increase of TPA content in the solids and the calcination temperature. The materials were found to be efficient and recyclable catalysts for the synthesis of a series of flavones. The reaction was carried out in different reaction media: heterogeneous and solvent-free conditions. The solvent-free conditions represent the best green conditions. Initially, we optimize the reaction condition to obtain 6-chloroflavone by direct reaction of the cyclodehydration of 1-(2-hydroxy-5-chlorophenyl)-3-phenyl-1,3-propanodione in the presence of a catalytic amount of mesoporous titania modified with tungstophosphoric acid catalyst. Reactions were performed in two conditions: low volume of toluene, at 110 °C, typically 24 h, and solvent-free at the same temperature, 1 h. In all cases the product (6-chloroflavone) was obtained with high selectivity. Conversions up to 76 and 92 % were obtained respectively, using the supported catalyst (TiTPA10). Optimal reaction conditions were applied to the preparation of six substituted flavones in both conditions.Facultad de Ciencias Agrarias y ForestalesCentro de Investigación y Desarrollo en Ciencias Aplicadas2013-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1433-1440http://sedici.unlp.edu.ar/handle/10915/139731enginfo:eu-repo/semantics/altIdentifier/issn/1380-2224info:eu-repo/semantics/altIdentifier/issn/1573-4854info:eu-repo/semantics/altIdentifier/doi/10.1007/s10934-013-9729-8info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:32:06Zoai:sedici.unlp.edu.ar:10915/139731Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:32:07.272SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
title Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
spellingShingle Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
Pérez, María Emilia
Ciencias Exactas
Química
Mesoporous titania modified with tungstophosphoric
Keggin heteropolyacids
Flavone synthesis
Solvent-free organic reaction
title_short Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
title_full Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
title_fullStr Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
title_full_unstemmed Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
title_sort Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones
dc.creator.none.fl_str_mv Pérez, María Emilia
Ruiz, Diego Manuel
Autino, Juan Carlos
Blanco, Mirta Noemí
Pizzio, Luis René
Romanelli, Gustavo Pablo
author Pérez, María Emilia
author_facet Pérez, María Emilia
Ruiz, Diego Manuel
Autino, Juan Carlos
Blanco, Mirta Noemí
Pizzio, Luis René
Romanelli, Gustavo Pablo
author_role author
author2 Ruiz, Diego Manuel
Autino, Juan Carlos
Blanco, Mirta Noemí
Pizzio, Luis René
Romanelli, Gustavo Pablo
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Química
Mesoporous titania modified with tungstophosphoric
Keggin heteropolyacids
Flavone synthesis
Solvent-free organic reaction
topic Ciencias Exactas
Química
Mesoporous titania modified with tungstophosphoric
Keggin heteropolyacids
Flavone synthesis
Solvent-free organic reaction
dc.description.none.fl_txt_mv Mesoporous TiO₂/H₃PW₁₂O₄₀ composites were synthesized by sol–gel reactions using urea as a low-cost template, and adding tungstophosphoric acid (TPA) at the same time as the template. The TPA concentration was varied in order to obtain TPA contents of 0, 10, and 20 (w/w) in the solid. The samples presented mesopores with a diameter higher than 3.0 nm. The specific surface area of the solids decreased with both the increase of the TPA content and the calcination temperature. From Fourier transform infrared and ³¹P magic angle spinning-nuclear magnetic resonance studies it was observed that the main heteropolyoxometallate species present in the composites is the [PW₁₂O₄₀]³⁻ anion, which was partially transformed into the [P₂W₂₁O₇₁]⁶⁻ and [PW₁₁O₃₉]⁷⁻ anions during the synthesis and drying step. The X-ray diffraction patterns of the modified samples only exhibited the characteristic peaks of the anatase phase of titanium oxide. The point of zero charge decreased with both the increase of TPA content in the solids and the calcination temperature. The materials were found to be efficient and recyclable catalysts for the synthesis of a series of flavones. The reaction was carried out in different reaction media: heterogeneous and solvent-free conditions. The solvent-free conditions represent the best green conditions. Initially, we optimize the reaction condition to obtain 6-chloroflavone by direct reaction of the cyclodehydration of 1-(2-hydroxy-5-chlorophenyl)-3-phenyl-1,3-propanodione in the presence of a catalytic amount of mesoporous titania modified with tungstophosphoric acid catalyst. Reactions were performed in two conditions: low volume of toluene, at 110 °C, typically 24 h, and solvent-free at the same temperature, 1 h. In all cases the product (6-chloroflavone) was obtained with high selectivity. Conversions up to 76 and 92 % were obtained respectively, using the supported catalyst (TiTPA10). Optimal reaction conditions were applied to the preparation of six substituted flavones in both conditions.
Facultad de Ciencias Agrarias y Forestales
Centro de Investigación y Desarrollo en Ciencias Aplicadas
description Mesoporous TiO₂/H₃PW₁₂O₄₀ composites were synthesized by sol–gel reactions using urea as a low-cost template, and adding tungstophosphoric acid (TPA) at the same time as the template. The TPA concentration was varied in order to obtain TPA contents of 0, 10, and 20 (w/w) in the solid. The samples presented mesopores with a diameter higher than 3.0 nm. The specific surface area of the solids decreased with both the increase of the TPA content and the calcination temperature. From Fourier transform infrared and ³¹P magic angle spinning-nuclear magnetic resonance studies it was observed that the main heteropolyoxometallate species present in the composites is the [PW₁₂O₄₀]³⁻ anion, which was partially transformed into the [P₂W₂₁O₇₁]⁶⁻ and [PW₁₁O₃₉]⁷⁻ anions during the synthesis and drying step. The X-ray diffraction patterns of the modified samples only exhibited the characteristic peaks of the anatase phase of titanium oxide. The point of zero charge decreased with both the increase of TPA content in the solids and the calcination temperature. The materials were found to be efficient and recyclable catalysts for the synthesis of a series of flavones. The reaction was carried out in different reaction media: heterogeneous and solvent-free conditions. The solvent-free conditions represent the best green conditions. Initially, we optimize the reaction condition to obtain 6-chloroflavone by direct reaction of the cyclodehydration of 1-(2-hydroxy-5-chlorophenyl)-3-phenyl-1,3-propanodione in the presence of a catalytic amount of mesoporous titania modified with tungstophosphoric acid catalyst. Reactions were performed in two conditions: low volume of toluene, at 110 °C, typically 24 h, and solvent-free at the same temperature, 1 h. In all cases the product (6-chloroflavone) was obtained with high selectivity. Conversions up to 76 and 92 % were obtained respectively, using the supported catalyst (TiTPA10). Optimal reaction conditions were applied to the preparation of six substituted flavones in both conditions.
publishDate 2013
dc.date.none.fl_str_mv 2013-12
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/139731
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info:eu-repo/semantics/altIdentifier/issn/1573-4854
info:eu-repo/semantics/altIdentifier/doi/10.1007/s10934-013-9729-8
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
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