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首页> 外文期刊>Revista de Chimie >Synthesis Characterization and Catalytic Activity of Some New Manganese (II) Compounds with Tetra-chloro R-bis(salicylaldehyde) Ethylenediamine and R- bis(salicylaldehyde) Phenylenediamine Ligands (R= H, CH3, CH2-CH3)
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Synthesis Characterization and Catalytic Activity of Some New Manganese (II) Compounds with Tetra-chloro R-bis(salicylaldehyde) Ethylenediamine and R- bis(salicylaldehyde) Phenylenediamine Ligands (R= H, CH3, CH2-CH3)

机译:四氯R-双(水杨醛)乙二胺和R-双(水杨醛)苯二胺配体(R = H,CH3,CH2-CH3)的一些新型锰(II)化合物的合成表征和催化活性

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摘要

The Schiff bases with two chlorine atoms grafted on each salicyl-aldehyde or salicyl-ketone molecules and with -H, -CH3 or CH3-CH2- in the azomethynic-position were synthesized as ligands. The chain between donors N-N atoms is either ethylene or -o-phenylene. The manganese (II) ion forms with such ligands coordinative compounds. The free ligands and manganese compounds were characterized by elemental analysis, UV-VIS, FT IR, NMR spectroscopy and cyclic voltammetry. The semi waves potentials are influenced of nature of substituents (Cl and R) grafted on the molecule of the ligands. These complexes are able to oxidize the 2,6-di-tert-butyi-phenol (DtBuP), in presence of molecular oxygen in DMF solution, with formation of the tetra-tert-butyl-diphenoquinone (TtBuDQ).
机译:合成了具有两个接枝在每个水杨醛或水杨基酮分子上的氯原子以及在甲亚甲基位置上带有-H,-CH3或CH3-CH2-的席夫碱作为配体。供体N-N原子之间的链是乙烯或-邻-亚苯基。锰(II)离子与这些配体形成配位化合物。游离配体和锰化合物通过元素分析,UV-VIS,FT IR,NMR光谱和循环伏安法进行表征。半波电势受接枝在配体分子上的取代基(Cl和R)的性质影响。这些络合物能够在DMF溶液中存在分子氧的情况下氧化2,6-二叔丁基苯酚(DtBuP),并形成四叔丁基-二苯醌(TtBuDQ)。

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