首页> 外文期刊>Inorganica Chimica Acta >Cu(II) and Ni(II) complexes based on monofunctional and dendrimeric pyrrole-imine ligands: Applications in catalytic liquid phase hydroxylation of phenol
【24h】

Cu(II) and Ni(II) complexes based on monofunctional and dendrimeric pyrrole-imine ligands: Applications in catalytic liquid phase hydroxylation of phenol

机译:基于单官能和树枝状吡咯-亚胺配体的Cu(II)和Ni(II)配合物:在酚的催化液相羟基化中的应用

获取原文
获取原文并翻译 | 示例
           

摘要

New bis(pyrrolide-imine) copper(II) and Ni(II) complexes Cl and C2 [{(C_3H_7)-N=CH(C_4H_3N)} _2Cu], [{(C_3H_7)-N=CH-(C_4H _3N)}_2Ni] as well as the bimetallic dendrimeric (pyrrolide-imine) copper(II) and nickel(II) complexes C3 and C4, [DAB-{(N=CH-C_4H_3N)_4}Cu_2], [DAB-{(N=CH-C_4H_3N)_2}Ni_2] (DAB-G1-polypropyleneimine dendrimer with a diaminobutane core) were prepared in good yields. The structure and composition of the complexes were confirmed by a combination of analytical techniques. These complexes were investigated as catalysts in the hydroxylation of phenol in aqueous media in the pH range of 2-6 for the mononuclear complexes, C1 and C2 while the bimetallic systems, C3 and C4 were studied over the pH range 2-8. H_2O_2 was used as the oxidant under an oxygen atmosphere. The copper systems generally showed higher activity as compared to their nickel analogues. Catechol was the predominant product followed by hydroquinone with small amounts of para-benzoquinone. The nickel complexes showed better selectivity for catechol. The pH of the reaction medium also plays a role in both activity and selectivity with pH 3 being optimal for activity and pH 6 for selectivity to catechol.
机译:新的双(吡咯化物-亚胺)铜(II)和Ni(II)络合物Cl和C2 [{(C_3H_7)-N = CH(C_4H_3N)} _2Cu],[{(C_3H_7)-N = CH-(C_4H _3N) } _2Ni]以及双金属树枝状(吡咯化物-亚胺)铜(II)和镍(II)配合物C3和C4,[DAB-{(N = CH-C_4H_3N)_4} Cu_2],[DAB-{(N = CH-C_4H_3N)_2} Ni_2](具有二氨基丁烷核的DAB-G1-聚丙烯亚胺树状大分子)以良好的产率制备。配合物的结构和组成通过分析技术的结合得到证实。研究了这些络合物作为单核络合物C1和C2在pH范围为2-6的水性介质中苯酚羟基化的催化剂,而在2-8的pH范围内研究了双金属体系C3和C4的情况。在氧气气氛下,将H_2O_2用作氧化剂。与镍类似物相比,铜系统通常表现出更高的活性。邻苯二酚是主要产物,其次是对苯二酚和少量对苯醌。镍配合物对儿茶酚具有更好的选择性。反应介质的pH值在活性和选择性中都起着作用,其中pH 3的活性最佳,而儿茶酚的选择性pH 6。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号