Synthesis, Characterization, X-Ray Crystal Structures, and Catalytic Epoxidation Activity of cis-Dioxomolybdenum(VI) and Oxovanadium(V) Complexes With N'-(2-Hydroxy-4-methoxybenzylidene)-4-trifluoromethylbenzohydrazide

Jing Liu, Jiahui Lin, Juan Liu, Wu Chen, Y. Cui
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引用次数: 4

Abstract

A new cis-dioxomolybdenum(VI) complex, [MoO2LMeOH] (1) and a new oxovanadium(V) complex, [VOL(OMe)MeOH] (2), with potentially tridentate ONO aroylhydrazone Schiff base derived from 4-methoxysalicylaldehyde with 4-trifluoromethylbenzohydrazide, have been synthesized and fully characterized on the basis of elemental analysis, FT-IR, molar conductivity, and electronic spectra. Structures of the complexes have been accomplished by single-crystal X-ray diffraction. The complexes have distorted octahedral structures in which the aroylhydrazones behave as binegative ligands. It is also revealed from the crystal structures that the Mo(VI) and V(V) centers adopt NO5 donor environment, and the octahedral coordination is furnished by oxido groups and oxygen atoms of methanol or deprotonated methanol molecules. The catalytic properties were investigated for epoxidation of cyclooctene using aqueous tert-butyl hydroperoxide as the oxidant.
N'-(2-羟基-4-甲氧基苄基)-4-三氟甲基苯并肼顺式二氧钼(VI)和钒(V)配合物的合成、表征、x射线晶体结构和催化环氧化活性
合成了一种新的顺式二氧钼(VI)配合物[MoO2LMeOH](1)和一种新的氧钒(V)配合物[VOL(OMe)MeOH](2),该配合物由4-甲氧基水杨酸醛和4-三氟甲基苯并肼衍生而成,具有潜在的三齿化合物ONO芳基腙希夫碱,并通过元素分析、FT-IR、摩尔电导率和电子能谱对其进行了充分的表征。配合物的结构已通过单晶x射线衍射完成。配合物具有扭曲的八面体结构,其中芳基腙表现为负配体。从晶体结构上也可以看出,Mo(VI)和V(V)中心采用NO5给体环境,八面体配位由甲醇或去质子化甲醇分子的氧化基和氧原子提供。以过氧化叔丁基为氧化剂,研究了环氧化环烯的催化性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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