Molybdenum(VI) dioxo complexes for the epoxidation of allylic alcohols and olefins

被引:17
作者
Pandhare, Swati L. [1 ]
Jadhao, Rajesh R. [1 ]
Puranik, Vedavati G. [2 ]
Joshi, Pranaya V. [2 ]
Capet, Frederic [3 ]
Dongare, Mohan K. [1 ]
Umbarkar, Shubhangi B. [1 ]
Michon, Christophe [3 ]
Agbossou-Niedercorn, Francine [3 ]
机构
[1] Natl Chem Lab, Pune 411008, Maharashtra, India
[2] CSIR Natl Chem Lab, Ctr Mat Characterizat, Pune 411008, Maharashtra, India
[3] Univ Lille Nord France, CNRS UMR 8181, Ecole Natl Super Chim Lille, Unite Catalyse & Chim Solide, Villeneuve Dascq, France
关键词
Allylic alcohol; Molybdenum; Oxidation; Epoxidation; Peroxide; SCHIFF-BASE LIGANDS; DIOXOMOLYBDENUM(VI) COMPLEXES; CATALYTIC APPLICATIONS; HYDROGEN-PEROXIDE; TUNGSTEN COMPLEXES; TERMINAL OXIDANT; ETA(5)-CYCLOPENTADIENYL MOLYBDENUM; ASYMMETRIC OXIDATIONS; ALKYL HYDROPEROXIDES; TRICARBONYL COMPLEX;
D O I
10.1016/j.jorganchem.2014.09.029
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Several molybdenum(VI) dioxo complexes have been investigated as catalyst precursors for allylic alcohol epoxidation using mainly hydrogen peroxide as oxidant. All catalysts proved to be efficient and selective for the epoxidation of allylic alcohols provided the olefins were rather electron rich. Indeed, electron poor substrates could be converted selectively into the corresponding unsaturated aldehydes. A chiral dioxomolybdenum complex based on an optically pure tridentate Schiff base ligand was synthesized and characterized. Though that complex provided an efficient epoxidation catalyst for allylic alcohols and olefins, no chiral induction was observed. During the X-ray diffraction analysis, the cooling at 100 K led to the appearance of super-lattice reflections on diffraction patterns reflecting an ordering of the structure. Instead of one organometallic species observed at 298 K, three similar complexes of the same molecular structure could be observed in the asymmetric unit at 100 K. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:271 / 279
页数:9
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