Issue 86, 2015

Direct covalent attachment of Mn(iii) salophen complex to the hydroxyapatite-encapsulated γ-Fe2O3 nanocrystallites: an efficient magnetic and reusable catalyst for oxidation of alcohols

Abstract

In the present work, the highly efficient oxidation of alcohols catalyzed by manganese(III) salophen acetate, [Mn(salophen)OAc], supported on hydroxyapatite coated magnetite nanoparticles, HAp–Fe2O3, is reported. First, the HAp–Fe2O3 nanoparticles were modified with 5-chloromethyl-2-hydroxybenzaldehyde and then using 1,2-diamino benzene, 2-hydroxybenzaldehyde and Mn(CH3COO)2·4H2O, [Mn(salophen)OAc] was synthesized and attached to the support via covalent linkages. The prepared catalyst was characterized by FT-IR spectroscopy, X-ray diffraction, diffuse reflectance UV-Vis spectrophotometry and scanning electron microscopy. This new heterogeneous catalyst was used for efficient oxidation of alcohols with NaIO4 at room temperature. This new heterogeneous catalyst is of high reusability in the oxidation reactions, in which the catalyst was reused several times without significant loss of its catalytic activity.

Graphical abstract: Direct covalent attachment of Mn(iii) salophen complex to the hydroxyapatite-encapsulated γ-Fe2O3 nanocrystallites: an efficient magnetic and reusable catalyst for oxidation of alcohols

Article information

Article type
Paper
Submitted
08 May 2015
Accepted
21 Jul 2015
First published
18 Aug 2015

RSC Adv., 2015,5, 70577-70585

Direct covalent attachment of Mn(III) salophen complex to the hydroxyapatite-encapsulated γ-Fe2O3 nanocrystallites: an efficient magnetic and reusable catalyst for oxidation of alcohols

A. Saffar-Teluri, RSC Adv., 2015, 5, 70577 DOI: 10.1039/C5RA08594B

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