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Journal of Materials Science

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09-07-2018 | Chemical routes to materials

Preparation, characterization and catalytic oxidation properties of silica composites immobilized with cationic metalloporphyrins

Authors: Dongbo Zhao, Yongsong Wang, Yujing Xu, Ning Wang, Jun Li

Published in: Journal of Materials Science | Issue 20/2018

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Abstract

Herein, the metalloporphyrins Co(II) (5, 10, 15, 20-tetra (4-(3-(N-ethyl-4-pyridyl)pyrazolyl)phenyl)porphyrin) (CoTEtPyP) and Mn(III) (5, 10, 15, 20-tetra(4-(3-(N-ethyl-4-pyridyl)pyrazolyl)phenyl)porphyrin) (MnTEtPyP(OAc)) were synthesized and characterized spectroscopically. The cationic metalloporphyrins were firstly immobilized on the surface of SiO₂ by electrostatic attractions with hydrothermal method to get the gels. Then, the gels were extracted by supercritical CO₂ to remove the redundant solvent molecules and the unreacted metal salt. The structures and properties of porphyrin–SiO₂ porous composites (PSC1 and PSC2) were characterized by Fourier transform infrared spectroscopy, ultraviolet–visible spectroscopy, scanning electron microscopy, transmission electron microscope, powder X-ray diffraction, thermalgravimetric analysis and nitrogen sorption measurements. N₂ absorptions have verified that the porous materials have large BET surface area and big N₂ uptake capacity. The composites also have shown higher specific surface area and superior thermal stability. The catalytic activities of the new PSCs to the ethylbenzene oxidation carried out indicated that both of them exhibit highly selectivity of acetophenone (> 99%) with the conversion of 87.6% (PSC1) and 93.0% (PSC2), respectively.

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Title: Preparation, characterization and catalytic oxidation properties of silica composites immobilized with cationic metalloporphyrins
Authors: Dongbo Zhao
Yongsong Wang
Yujing Xu
Ning Wang
Jun Li
Publication date: 09-07-2018
Publisher: Springer US
Published in: Journal of Materials Science / Issue 20/2018
Print ISSN: 0022-2461
Electronic ISSN: 1573-4803
DOI: https://doi.org/10.1007/s10853-018-2662-0

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