Diferric oxo-bridged complexes of a polydentate aminopyridyl ligand: synthesis, structure and catalytic reactivity

被引:6
|
作者
Kejriwal, Ambica [1 ]
Biswas, Achintesh Narayan [2 ]
Choudhury, Amitava [3 ]
Bandyopadhyay, Pinaki [1 ]
机构
[1] Univ N Bengal, Dept Chem, Raja Rammohunpur 734013, Siliguri, India
[2] Siliguri Coll, Dept Chem, Siliguri 734001, India
[3] Missouri Univ Sci & Technol, Dept Chem, Rolla, MO 65409 USA
关键词
CRYSTAL-STRUCTURE; METHANE MONOOXYGENASE; DIOXYGEN ACTIVATION; DIAMOND CORE; OXIDATION; H2O2; HYDROXYLATION; N,N'-DIMETHYL-N,N'-BIS(2-PYRIDYLMETHYL)ETHANE-1,2-DIAMINE; HYDROCARBONS; MECHANISM;
D O I
10.1007/s11243-014-9875-0
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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 A mu-oxo diiron(III) complex [Fe(bpmen)(A mu-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 A mu-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)(A mu-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.
引用
收藏
页码:909 / 915
页数:7
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