首页> 外文期刊>Inorganica Chimica Acta >Synthesis, characterization and reactivity of a series of dinuclear copper complexes bearing the ligand bis[3-(2-hydroxybenzylideneamino)phenyl] sulfone and derivatives
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Synthesis, characterization and reactivity of a series of dinuclear copper complexes bearing the ligand bis[3-(2-hydroxybenzylideneamino)phenyl] sulfone and derivatives

机译:一系列带有配体双[3-(2-羟基亚苄基氨基)苯基]砜及其衍生物的双核铜配合物的合成,表征和反应性

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The ligands bis[3-(X-2-hydroxybenzylideneamino)phenyl] sulfones (X = none: BHBAPS, X = 3-tert-butyl: BH(t-Bu)BAPS and X = 3,5-dichloro: BHCl(2)BAPS) were prepared. These, together with Cu(OAc)(2) were used in the syntheses of the dinuclear copper complexes Cu-2(BBAPS)(mu -OMe)(2) (1), Cu-2[B(t-Bu)BAPS] (mu -OH)(2) (2), and Cu-2[BCl(2)BAPS] (mu -OMe)(2) (3). Complex 1 was crystallographically characterized. The structures of 2 and 3 are similar to 1 by comparison of IR, UV-Vis, FAB-MS and elemental analyses results. Complexes 1-3 (1 mol%) were used in the oxidation of 2,4- and 2,6-di-t-butylphenol (dtbp) at -50 degreesC with H2O2. The results show that (1) the coupling products are preferred when CH2Cl2 is used; and (2) the quinone yield increases when THF is utilized. In CH2Cl2 with 2,4-dtbp, the yield of the coupling product based on the complex amount, is in the order 2, 1, and 3 with yields of 6300, 4700 and 200%, respectively, Low temperature UV-Vis results of the reaction of 1 with H2O2 showed the growth of peaks at 390 and 580 nm indicative of a mu-eta (2):eta (2)-peroxo or mu-eta (1):eta (1)-hydroperoxo intermediate. At -50 degreesC, this spectrum does not change. But when warmed to 0 degreesC, a spectrum similar to the original spectrum was obtained. This probably indicates hydrogen radical abstractions of the peroxo intermediate from solvents, and if excess H2O2 is present, the peroxo intermediate may again be formed. This reusability of the complex explains the high yield using 1 and 2. (C) 2001 Elsevier Science B.V. All rights reserved. [References: 25]
机译:配体双[3-(X-2-羟基苄叉基氨基)苯基]砜(X =无:BHBAPS,X = 3-叔丁基:BH(t-Bu)BAPS,X = 3,5-二氯:BHCl(2准备)这些与Cu(OAc)(2)一起用于双核铜络合物Cu-2(BBAPS)(mu -OMe)(2)(1),Cu-2 [B(t-Bu)BAPS ](μ-OH)(2)(2)和Cu-2 [BCl(2)BAPS](μ-OMe)(2)(3)。对配合物1进行了晶体学表征。通过比较IR,UV-Vis,FAB-MS和元素分析结果,2和3的结构与1相似。配合物1-3(1 mol%)用于在-50°C下用H2O2氧化2,4-和2,6-二叔丁基苯酚(dtbp)。结果表明:(1)当使用CH2Cl2时,偶合产物是优选的; (2)当使用THF时,醌产率增加。在具有2,4-dtbp的CH2Cl2中,基于复合量的偶联产物的收率约为2、1和3,分别为6300、4700和200%,低温UV-Vis结果为1与H2O2的反应表明在390和580 nm处出现峰增长,表明存在mu-eta(2):eta(2)-过氧或mu-eta(1):eta(1)-氢过氧中间体。在-50摄氏度下,该光谱不变。但是当加热到0℃时,获得了类似于原始光谱的光谱。这可能表明过氧中间体从溶剂中夺取了氢自由基,如果存在过量的H2O2,则可能再次形成过氧中间体。该复合物的可重复使用性说明了使用1和2可以实现高产量。(C)2001 Elsevier Science B.V.保留所有权利。 [参考:25]

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