Oxoperoxo molybdenum(VI)- and tungsten(VI) complexes with 1-(2′-hydroxyphenyl) ethanone oxime: Synthesis, structure and catalytic uses in the oxidation of olefins, alcohols, sulfides and amines using H2O2 as a terminal oxidant

被引:92
作者
Gharah, Narottam [1 ]
Chakraborty, Santu [2 ]
Mukherjee, Alok K. [2 ]
Bhattacharyya, Ramgopal [1 ]
机构
[1] Jadavpur Univ, Dept Chem, Kolkata 700032, W Bengal, India
[2] Jadavpur Univ, Dept Phys, Kolkata 700032, W Bengal, India
关键词
Synthesis; Crystal structure; Catalysis; Epoxidation; Oxoperoxo molybdenum and tungsten; Alcohol; amine and sulfide oxidation; OXYGEN-ATOM TRANSFER; HIGHLY EFFICIENT EPOXIDATION; 30-PERCENT HYDROGEN-PEROXIDE; ELECTRON-DEFICIENT OLEFINS; METHYLRHENIUM TRIOXIDE; METAL CATALYSIS; ASYMMETRIC EPOXIDATION; ENVIRONMENTALLY BENIGN; CRYSTAL-STRUCTURE; HYDROXAMIC ACIDS;
D O I
10.1016/j.ica.2008.05.017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
High yield synthesis of two new oxodiperoxo-molybdate, PPh4[MoO(O-2)(2)(HPEOH)] (1), and -tungstate, PPh4[WO(O-2)(2)(HPEOH)] (2), complexes with 1-(2'-hydroxyphenyl) ethanone oxime (HPEOH2) as organic ligand has been achieved by adding methanol solution of the ligand to the pale-yellow solution obtained by dissolving molybdic-/tungstic-acid (freshly prepared) in hydrogen peroxide and precipitating the complexes using tetraphenylphosphonium chloride. The orange-yellow complexes have been characterized by elemental analysis, IR, H-1 NMR, UV-Vis spectroscopy and. finally by X-ray structure analysis. Both the complexes function as facile olefin epoxidation catalysts with hydrogen peroxide as terminal oxidant and bicarbonate as a co-catalyst at room temperature. Catalytic potentiality of 1 and 2 is also exhibited in the case of oxidation of alcohols, amines and sulfides. The catalysts are very much efficient especially in olefin epoxidation giving high yield, TON (turnover number) and TOF (turnover frequency). The method described is environmentally benign and cost-effective in all the cases. (C) 2008 Elsevier B. V. All rights reserved.
引用
收藏
页码:1089 / 1100
页数:12
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