Artigo Revisado por pares

Manganeseporphyrin-catalyzed alkenes epoxidation by iodobenzene diacetate in a room temperature ionic liquid

2003; Elsevier BV; Volume: 252; Issue: 1 Linguagem: Inglês

10.1016/s0926-860x(03)00376-4

ISSN

1873-3875

Autores

Z. Li,

Tópico(s)

Polyoxometalates: Synthesis and Applications

Resumo

Abstract Catalytic epoxidation of alkenes with iodobenzene diacetate by the manganeseporphyrin in environmentally benign and ambient temperature ionic liquid 1-n-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF6) has been studied. The use of [bmim]PF6 as the reaction medium brought definitive advantages over an organic catalytic phase: the reaction proceeded with high efficiency and the rate was much higher than that of in CH2Cl2; the ionic liquid–manganeseporphyrin system could be reused at least 12 times without losing activity. The mechanism of the reaction was also investigated.

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