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首页> 外文期刊>Inorganica Chimica Acta >Vanadyl tetradentate Schiff base complexes as catalyst for C-H bond activation of olefins with tert-butylhydroperoxide: Synthesis, characterization and structure
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Vanadyl tetradentate Schiff base complexes as catalyst for C-H bond activation of olefins with tert-butylhydroperoxide: Synthesis, characterization and structure

机译:钒基四齿席夫碱配合物作为叔丁基氢过氧化物活化烯烃的C-H键的催化剂:合成,表征和结构

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摘要

Three N2O2 tetradentate Schiff base ligands (H2L1-3) were prepared by reaction of 1,2-propylenediamine and appropriate aldehyde and ketone and characterized by FT-IR, H-1 and C-13 NMR. The vanadyl complexes were synthesized by treating an ethanolic solution of the appropriate ligand and one equivalent of VO(acac)(2) to yield VOL1-3. These oxovanadium (IV) complexes were characterized on the basis of their FT-IR, UV-Vis spectroscopy and elemental analysis. The crystal structure of VOL3 has been determined. The metal center in VOL3 is a deformed tetragonal pyramidal N2O3 coordination sphere. These complexes are used as catalyst for the selective epoxidation of olefins. High selectivity of epoxidation for cyclooctene observed from oxidation data. The catalytic activity increases as the number of electron-donor groups increases, and the catalytic selectivity is varied by changing the substituents on the ligands. The catalytic system described here is an efficient and inexpensive method for the oxidation of olefins, with the advantages of high activity, selectivity, re-usability and short reaction time. (C) 2007 Elsevier B.V. All rights reserved.
机译:通过1,2-丙二胺与适当的醛和酮反应制备了三个N2O2四齿席夫碱配体(H2L1-3),并通过FT-IR,H-1和C-13 NMR进行了表征。通过处理适当配体的乙醇溶液和一当量的VO(acac)(2)合成钒基配合物,生成VOL1-3。这些氧钒(IV)配合物的特征在于其FT-IR,UV-Vis光谱和元素分析。 VOL3的晶体结构已经确定。 VOL3中的金属中心是变形的四角锥N2O3配位球。这些络合物用作烯烃选择性环氧化的催化剂。从氧化数据观察到环辛烯对环氧化的高选择性。随着电子给体基团数目的增加,催化活性也增加,并且通过改变配体上的取代基来改变催化选择性。本文所述的催化系统是一种高效且廉价的烯烃氧化方法,具有高活性,选择性,可重复使用性和短反应时间的优点。 (C)2007 Elsevier B.V.保留所有权利。

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