CATALYTIC EPOXIDATION OF CYCLOHEXENE WITH TERT-BUTYLHYDROPEROXIDE USING AN IMMOBILIZED MOLYBDENUM CATALYST

This work describes the synthesis of molybdenum complexes immobilized on a silica support and their performance in the epoxidation reaction of cyclohexene using tert-butylhydroperoxide (TBHP) as the oxidizing agent. The catalyst synthesis included solubilization of variable amounts of bis-oxomolybde...

ver descrição completa

Detalhes bibliográficos
Autores: Morales-delaRosa, Silvia, Campos Martín, José Miguel, Terreros Ceballos, Pilar, García Fierro, José Luis
Formato: artículo
Estado:Versión enviada para evaluación y publicación
Fecha de publicación:2015
País:España
Recursos:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/116372
Acesso em linha:http://hdl.handle.net/10261/116372
Access Level:acceso abierto
Palavra-chave:Epoxidation
molybdenum
immobilized catalysts
tertbutylhydroperoxide
Descrição
Resumo:This work describes the synthesis of molybdenum complexes immobilized on a silica support and their performance in the epoxidation reaction of cyclohexene using tert-butylhydroperoxide (TBHP) as the oxidizing agent. The catalyst synthesis included solubilization of variable amounts of bis-oxomolybdenum (VI) acetylacetonate precursor in different solvents such as tetrahydrofuran (THF), ethanol, THF/water and ethanol/water mixtures and contact with the silica support. Characterization techniques demonstrated that the nature of the incorporated molybdenum species depends markedly on the solvent employed. If the solvent employed is an ethanol:water mixture, physical adsorption of the Mo-species onto the support surface occurs; however, when THF is used as the solvent (THF catalyst series), molybdenum is grafted on the silica surface via chemical bonding with the surface hydroxyl groups of silica. Specifically, these latter catalysts show similar performance to that of the homogeneous catalyst, although long-term experiments showed deactivation by leaching of the active phase.