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

被引:5
|
作者
Liu, Jing [1 ]
Lin, Jiahui [1 ]
Liu, Juan [1 ]
Chen, Wu [1 ,2 ]
Cui, Yongming [3 ]
机构
[1] Wuhan Text Univ, Sch Textile Sci & Engn, Wuhan, Peoples R China
[2] Wuhan Text Univ, Minist Educ, Key Lab Text Fibers & Prod, Wuhan, Peoples R China
[3] Wuhan Text Univ, Sch Environm Engn, Wuhan 430073, Peoples R China
关键词
dioxomolybdenum(VI); oxovanadium(V); aroylhydrazone; Schiff base; X-ray crystal structure; catalytic epoxidation activity; SCHIFF-BASE COMPLEXES; OLEFIN EPOXIDATION; OXOMOLYBDENUM(VI) COMPLEXES; MOLYBDENUM(VI) COMPLEX; DONOR LIGANDS; COPPER(II); OXIDATION; CARBONYL; MODEL;
D O I
10.1080/15533174.2015.1137075
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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.
引用
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页码:1871 / 1878
页数:8
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