Synthesis, single crystal structures and efficient catalysis for tetralin oxidation of two novel complexes of Cu(II) with 2-aminomethyl pyridine

被引:11
|
作者
Wang, Chunling [1 ]
Zhang, Yuecheng [1 ]
Yuan, Baoguo [1 ]
Zhao, Jiquan [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Tianjin 300130, Peoples R China
关键词
Tetralin; alpha-Tetralone; Oxidation; tert-Butyl hydroperoxide; Cu(II) complex; TERT-BUTYL HYDROPEROXIDE; MCM-41; MOLECULAR-SIEVES; ALLYLIC OXIDATION; PRIMARY ALCOHOLS; COPPER; OXYGEN; CYCLOHEXANE; PEROXIDES; BENZENE; ALKENES;
D O I
10.1016/j.molcata.2010.10.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two novel Cu(II) complexes were synthesized through the reaction of 2-aminomethyl pyridine (AMP) with CuCl2 center dot 2H(2)O by changing the metal/ligand ratio. Their structures were thoroughly characterized by FT-IR, elemental analysis and X-ray diffraction method. The results revealed that complex 1 [Cu(AMP)Cl-2] consists of isolated binuclear molecules unit and displays distorted tetragonal pyramid. Complex 2 [Cu(AMP)(2)(H2O)(2)]Cl-2 exhibits a octahedral geometry. The complexes were both evaluated as catalysts in the tetralin oxidation with TBHP as oxidant. Complex 1 showed high catalytic activity and selectivity towards alpha-tetralone under mild conditions. Thus, under the optimized conditions (acetonitrile 10 ml, catalyst 0.045 mmol, tetralin 4.5 mmol, 65% TBHP 22.5 mmol, T = 50 degrees C), the conversion of tetralin reached 89% with a selectivity of 71% towards alpha-tetralone. Compared with complex 1, complex 2 displayed low catalytic activity mainly due to the strong steric hindrance from the two coordinated 2-aminomethyl pyridine molecules. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:173 / 179
页数:7
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