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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/139731
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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 Articulo 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://sedici.unlp.edu.ar/handle/10915/139731 |
url |
http://sedici.unlp.edu.ar/handle/10915/139731 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/1380-2224 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 |
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http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
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