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Immobilization of manganoporphyrin on a novel polymeric support and catalytic oxidation characteristic of supported catalyst

✍ Scribed by Baojiao Gao; Ruixin Wang; Yan Zhang


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
484 KB
Volume
112
Category
Article
ISSN
0021-8995

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✦ Synopsis


Abstract

Monomer glycidyl methacrylate (GMA) was grafted on silica gel particles in the manner of “grafting from,” and the grafted particles PGMA/SiO~2~ was prepared. The grafted particles PGMA/SiO~2~ is a kind of novel support for the immobilization of metalloporphyrin catalysts. In the presence of basic catalysts, the ring‐opening reaction of the epoxy groups of the grafted PGMA occurred and the bonding of meso‐tetra (4‐hydroxylphenyl) porphyrin (THPP) on the particles PGMA/SiO~2~ was realized, resulting in the bonded particles HPP‐PGMA/SiO~2~. Subsequently, the metallation of the bonded particles HPP‐PGMA/SiO~2~ was carried out via the coordination reaction between HPP‐PGMA/SiO~2~ and manganese salt, resulting in the supported manganoporphyrin (MnP) catalyst MnP‐PGMA/SiO~2~. The supported catalyst was used in the catalytic oxidation of ethyl benzene into acetophenone by molecular oxygen. In this article, the effects of various factors such as the species and amount of the catalyst on the bonding process of THPP were studied because of the importance of the bonding reaction of THPP in the preparation of the catalyst MnP‐PGMA/SiO~2~. Finally, the catalytic performance of MnP‐PGMA/SiO~2~ in the catalytic oxidation process of ethyl benzene was investigated. The experimental results show that triethylamine is a suitable catalyst for the bonding of THPP on the grafted particles PGMA/SiO~2~ and for the forming of MnP‐PGMA/SiO~2~. The supported catalyst MnP‐PGMA/SiO~2~ can effectively activate molecular oxygen, and obviously catalyze the oxidation process of ethyl benzene to acetophenone by molecular oxygen. It was found that the immobilization density of MnP on MnP‐PGMA/SiO~2~ has a great effect on the catalytic activity of the catalyst. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009


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