A hybrid system bases on silica-alumina and Keggin heteropolyacids as catalyst in the suitable 2-(2-furyl)-chromones and chromanones synthesis

Molybdophosphoric acid/silica-alumina composites are synthesized a through a process described, in which the heteropolyacid was impregnated on different silica-aluminas, obtained by sol-gel. Three different techniques were used to prepare the samples. The catalysts were prepared by incipient wetness...

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Autores:
Tipo de recurso:
Fecha de publicación:
2022
Institución:
Universidad Pedagógica y Tecnológica de Colombia
Repositorio:
RiUPTC: Repositorio Institucional UPTC
Idioma:
spa
OAI Identifier:
oai:repositorio.uptc.edu.co:001/15351
Acceso en línea:
https://revistas.uptc.edu.co/index.php/ciencia_en_desarrollo/article/view/14165
https://repositorio.uptc.edu.co/handle/001/15351
Palabra clave:
Keggin heteropolyacids, Silica-alumina, Sol–gel synthesis, 2-(2-Furyl)-chromones, 2-(2-Furyl)-chromanones
Keggin heteropolyacids, Silica-alumina, Sol–gel synthesis, 2-(2-Furyl)-chromones, 2-(2-Furyl)-chromanones
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License
http://purl.org/coar/access_right/c_abf2
Description
Summary:Molybdophosphoric acid/silica-alumina composites are synthesized a through a process described, in which the heteropolyacid was impregnated on different silica-aluminas, obtained by sol-gel. Three different techniques were used to prepare the samples. The catalysts were prepared by incipient wetness impregnation and different thermal treatments were applied. The hybrid systems were characterized by using SBET, DRX, XRD and acidity measurements.  The catalytic activity of these materials was tested in the solvent-free cyclization of 1-(2-hydroxyphenyl)-3-(2-furyl)-1,3-propanedione to 2-(2-furyl)-chromones. The transformation gives very good yields of product, free of secondary products. Environmental benign procedure, and easy catalyst separation, is relevant features of this methodology. In this way the catalyst can be used and reused six cycles without loss of catalytic activity. The most active catalyst was also used in the solvent-free cyclization of 1-(2-hydroxyphenyl)-3-(2-furyl)-2-propen-1-one and the methodology can be extended to the synthesis of other 2-(2-(furyl)-chromones and chromanones. The green context for this new procedure was confirmed by greenmetrics parameters.