Cu(II) and Mn(II) Anchored on Functionalized Mesoporous Silica with Schiff Bases: Effects of Supports and Metal–Ligand Interactions on Catalytic Activity

Author:

Mureseanu Mihaela1,Filip Mihaela2,Bleotu Irina1,Spinu Cezar Ionut1,Marin Alexandru Horia34ORCID,Matei Iulia2ORCID,Parvulescu Viorica2

Affiliation:

1. Department of Chemistry, Faculty of Sciences, University of Craiova, Calea Bucuresti, 107I, 200478 Craiova, Romania

2. “IlieMurgulescu” Institute of Physical Chemistry, Romanian Academy, Splaiul Independentei 202, 060021 Bucharest, Romania

3. Ken and Mary Alice Lindquist Department of Nuclear Engineering, Penn State University, University Park, State College, PA 16802, USA

4. Surface Analysis Laboratory, Institute for Nuclear Research Pitesti, 115400 Mioveni, Romania

Abstract

New series of Cu(II) and Mn(II) complexes with Schiff base ligands derived from 2-furylmethylketone (Met), 2-furaldehyde (Fur), and 2-hydroxyacetopheneone (Hyd) have been synthesized in situ on SBA-15-NH2, MCM-48-NH2, and MCM-41-NH2 functionalized supports. The hybrid materials were characterized by X-ray diffraction, nitrogen adsorption–desorption, SEM and TEM microscopy, TG analysis, and AAS, FTIR, EPR, and XPS spectroscopies. Catalytic performances were tested in oxidation with the hydrogen peroxide of cyclohexene and of different aromatic and aliphatic alcohols (benzyl alcohol, 2-methylpropan-1-ol, and 1-buten-3-ol). The catalytic activity was correlated with the type of mesoporous silica support, ligand, and metal–ligand interactions. The best catalytic activity of all tested hybrid materials was obtained in the oxidation of cyclohexene on SBA-15-NH2-MetMn as a heterogeneous catalyst. No leaching was evidenced for Cu and Mn complexes, and the Cu catalysts were more stable due to a more covalent interaction of the metallic ions with the immobilized ligands.

Publisher

MDPI AG

Subject

General Materials Science,General Chemical Engineering

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