Abstract

In this study, we improved the catalytic performance of manganese porphyrin encapsulated HY zeolite for alkene epoxidation reaction. For this purpose, Manganese tetra pyridyl porphyrin encapsulated into modified dealuminated Y zeolite (MnTPP-MDAZY) was synthesized using zeolite template synthesis method. This heterogenized catalyst was characterized by FT-IR, UV–Vis, XRD and atomic absorption spectra (AAS) technique. Catalyst loading was 0.263 mmol/g support. In this way, high catalyst loading is probably related to the decrease of the size of metalloporphyrin and the post-synthesis treatment. The latter one causes the increase of the diameter of the mesoporous structure as a result of the dealumination of zeolite with EDTA treatment. High catalyst loading efficiently enhances the epoxidation of alkenes.

Highlights

  • IntroductionIn the post-synthesis treatment, secondary mesoporous structure is formed using the dealumination of zeolite [7, 10, 15,16,17]

  • Zeolite-encapsulated metal complexes have attracted special attention as modern catalytic systems and as model compounds for enzyme mimicking [1]

  • In this study, we improved the catalytic performance of manganese porphyrin encapsulated HY zeolite for alkene epoxidation reaction

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Summary

Introduction

In the post-synthesis treatment, secondary mesoporous structure is formed using the dealumination of zeolite [7, 10, 15,16,17] It leads to high Si/Al ratio and the replacement of large macromolecules such as porphyrin in the supercage of zeolite becomes possible [18]. The dealuminated sample was washed with hot distilled water dried and was used in the synthesis of manganese porphyrin inside nanocage of zeolite [22]. To prepare manganese tetra pyridyl porphyrin in the supercages of zeolite, 900 ll (equal 0.873 g) pyrrol, 1,320 ll (equal 1.386 g) fresh distilled benzaldehyde and 2 g MDAZY were mixed in 50 ml with propionic acid according to the reported procedure (Scheme 1) [22]. The crude filtrates were purified on a silicagel plate or a silica-gel column and identified by IR and 1H NMR spectral data

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