Oxidation of cyclohexanol to epsilon-caprolactone with aqueous hydrogen peroxide on H3PW12O40 and Cs2.5H0.5PW12O40

Liquid phase cyclohexanol catalytic oxidation to cyclohexanone and epsilon(ε)-caprolactone were studied using aqueous hydrogen peroxide as oxidant and H3PW12O40 (HPA) and H0.5Cs2.5PW12O40 (Cs-salt) as catalysts. The hydrophobic and insoluble Cs-salt showed the highest activity (per unit catalytic we...

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Detalles Bibliográficos
Autores: Balbinot, L., Schuchardt, U., Vera, Carlos Roman, Sepúlveda, Juan
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2008
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/65307
Acceso en línea:http://hdl.handle.net/11336/65307
Access Level:acceso abierto
Palabra clave:Cyclohexanol
Caprolactone
Heteropolyacid
https://purl.org/becyt/ford/2.7
https://purl.org/becyt/ford/2
Descripción
Sumario:Liquid phase cyclohexanol catalytic oxidation to cyclohexanone and epsilon(ε)-caprolactone were studied using aqueous hydrogen peroxide as oxidant and H3PW12O40 (HPA) and H0.5Cs2.5PW12O40 (Cs-salt) as catalysts. The hydrophobic and insoluble Cs-salt showed the highest activity (per unit catalytic weight and turnover number) and selectivity to (ε)-caprolactone. The ultrafine Cs-salt crystallites could be filtrated and recycled. Solvent effects on the activity and selectivity and the rate of peroxide decomposition were assessed and they were correlated to their polarity and protic/aprotic nature. When employing acetonitrile at 90 °C the highest activity and selectivity were achieved and also the lowest rate of hydrogen peroxide decomposition.