New copper(II) dimer with 3-(2-hydroxy-4-nitrophenylhydrazo)pentane-2,4-dione and its catalytic activity in cyclohexane and benzyl alcohol oxidations

被引:77
作者
Mahmudov, Kamran T. [1 ]
Kopylovich, Maximilian N. [1 ]
Guedes da Silva, M. Fatima C. [1 ,2 ]
Figiel, Pawel J. [1 ]
Karabach, Yauhen Yu. [1 ]
Pombeiro, Armando J. L. [1 ]
机构
[1] Univ Tecn Lisboa, Inst Super Tecn, Ctr Quim Estrutural, P-1049001 Lisbon, Portugal
[2] Univ Lusofona Humanidades & Tecnol, P-1749024 Lisbon, Portugal
关键词
3-(2-Hydroxy-4-nitrophenylhydrazo)pentane-2,4-dione complexes; Azoderivatives of beta-diketones; Copper; X-ray structure; Oxidation of cyclohexane; Oxidation of benzyl alcohol; TEMPO; MILD PEROXIDATIVE OXIDATION; AEROBIC OXIDATION; PHOTOMETRIC-DETERMINATION; SELECTIVE OXIDATION; HYDROGEN-PEROXIDE; AZO DERIVATIVES; COMPLEXES; ALKANES; TRIETHANOLAMINE; REAGENT;
D O I
10.1016/j.molcata.2009.11.006
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
3-(2-Hydroxy-4-nitrophenylhydrazo)pentane-2,4-dione (H2L, 1)was synthesized by azocoupling of diazonium salts of 2-hydroxy-4-nitroaniline with pentane-2,4-dione and shown to exist in the hydrazone tautomeric form in the free state and in its new dicopper(II)complex [Cu-2(H2O)(2)(mu-L)(2)] (2) whose X-ray crystal structure was determined. Complex 2 acts as a catalyst, under mild conditions, for the peroxidative oxidation (with H2O2) of cyclohexane to cyclohexanol, cyclohexanone and cyclohexyl hydroperoxide, in MeCN/H2O, and for the aerobic TEMPO-mediated selective oxidation of benzylic alcohols to the corresponding aldehydes, thus showing that azoderivatives of beta-diketones can be the suitable ligands for such types of reactions. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 50
页数:7
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