Mononuclear and dinuclear salen type copper(II) Schiff base complexes: Synthesis, characterization, crystal structures and catalytic epoxidation of cyclooctene

被引:48
|
作者
Abbasi, Zeinab [1 ]
Behzad, Mahdi [1 ]
Ghaffari, Abolfazl [1 ]
Rudbari, Hadi Amiri [2 ]
Bruno, Giuseppe [3 ]
机构
[1] Semnan Univ, Dept Chem, Semnan 3535119111, Iran
[2] Univ Isfahan, Fac Chem, Esfahan 8174673441, Iran
[3] Univ Messina, Dip Sci Chim, I-98166 Messina, Italy
关键词
Copper(II); Schiff base; Crystal structure; Dinuclear; Epoxidation; OXIDATION; LIGANDS; ELECTROCHEMISTRY;
D O I
10.1016/j.ica.2014.01.047
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of salen type Schiff base ligands and their mononuclear (CuLn, n = 1-4) or dinuclear Cu(II) complexes (Cu-2(L-5)(2)) were synthesized and characterized by H-1 NMR, IR and UV-Vis spectroscopy as well as elemental analyses. The ligands were synthesized from the condensation of meso-1,2-diphenyl-1,2-ethylenediamine with various salicylaldehyde derivatives (x-salicylaldehyde for H2Ln, x = H (n = 1), 5-Br (n = 2), 5-Br-3-NO2 (n = 3), 3-OMe, (n = 5)) and 20-hydroxyacetophenone (n = 4). Crystal structures of two complexes (CuL4 and Cu-2(L-5)(2)) were determined. Catalytic performance of the complexes was studied in the epoxidation of cyclooctene using tert-butylhydroperoxide (TBHP) as oxidant. Various factors including reaction temperature, solvent type, time, catalyst amount and substrate to oxidant ratio were optimized. High catalytic activity and epoxides selectivity was found. Solvent free epoxidation of cyclooctene was also studied and higher catalytic activity, epoxide selectivity and lower reaction times were observed. (C) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
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