Diferric Oxo-Bridged Complexes of a Polydentate Aminopyridyl Ligand: Synthesis, Structure and Catalytic Reactivity
Abstract
The catalytic reactivity of a group of diferric oxo-bridged complexes (1-3) of a tetradentate ligand (bpmen = N,N'-dimethyl-N,N'-bis(2-pyridylmethyl)-1,2-diaminoethane) toward alkane hydroxylation has been evaluated. Among the three complexes, the µ-oxo diiron(III) complex [Fe(bpmen)(µ-O)FeCl3] (1) has been synthesized for the first time. The complex 1 has been characterized by spectroscopic analysis and X-ray crystallography. At room temperature, the µ-oxo diiron(III) complexes 1-3 have been found to be useful catalysts in hydroxylation of alkanes with m-chloroperbenzoic acid as oxidant. [Fe(bpmen)(µ-O)FeCl3] (1) has been found to be the most active catalyst. Moreover, the catalytic ability of the complexes in the oxidation of alcohols to ketones with hydrogen peroxide at room temperature has also been investigated.
Recommended Citation
A. Kejriwal et al., "Diferric Oxo-Bridged Complexes of a Polydentate Aminopyridyl Ligand: Synthesis, Structure and Catalytic Reactivity," Transition Metal Chemistry, vol. 39, no. 8, pp. 909 - 915, Springer International Publishing, Sep 2014.
The definitive version is available at https://doi.org/10.1007/s11243-014-9875-0
Department(s)
Chemistry
Keywords and Phrases
Catalysts; Catalytic oxidation; Chelation; Crystallography; Hydroxylation; Ketones; Ligands; Paraffins; Spectroscopic analysis; Synthesis (chemical); X ray crystallography; Active catalyst; Alkane hydroxylations; Catalytic ability; Catalytic reactivity; M-chloroperbenzoic acid; Oxidation of alcohols; Room temperature; Tetradentate ligands; Iron compounds
International Standard Serial Number (ISSN)
0340-4285; 1572-901X
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2014 Springer International Publishing, All rights reserved.
Publication Date
01 Sep 2014