OH-substituted tridentate ONO Schiff base ligands and related molybdenum(VI) complexes for solvent-free (ep)oxidation catalysis with TBHP as oxidant

被引:29
|
作者
Wang, Weili [1 ,2 ]
Daran, Jean-Claude [1 ]
Poli, Rinaldo [1 ,3 ]
Agustin, Dominique [1 ,2 ]
机构
[1] Univ Toulouse, UPS, INPT, CNRS,LCC, 205 Route Narbonne, F-31077 Toulouse, France
[2] Univ Toulouse, Inst Univ Technol Paul Sabatier, Dept Chim, Ave Georges Pompidou,BP 20258, F-81104 Castres, France
[3] Inst Univ France, 103 Bd St Michel, F-75005 Paris, France
关键词
Molybdenum; Solvent-free; Epoxidation; DFT; X-ray structures; DINUCLEAR DIOXOMOLYBDENUM(VI) COMPLEXES; MOLECULAR-ORBITAL METHODS; GAUSSIAN-TYPE BASIS; X-RAY-STRUCTURE; CRYSTAL-STRUCTURE; DIOXO COMPLEXES; BASIS-SETS; EPOXIDATION; MONONUCLEAR; OXO-VANADIUM(V);
D O I
10.1016/j.molcata.2016.02.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Molybdenum complexes with ONO tridentate Schiff base ligands based on salicylideneaminophenolato (SAP) backbone with OH substitution on the salicyl arene ring have been synthesized and characterized. The molecular structures of the full series of OH substituted molybdenum complexes were determined by X-ray crystallography as monomers stabilized by one solvent molecule, [MoO2L(D)]. All dimeric complexes [MoO2L](2) were tested for the epoxidation of cyclooctene and cyclohexene under organic solvent-free conditions using aqueous TBHP as oxidant. The position of the OH on the SAP-modified ligand influenced the catalytic activity of the respective complexes. DFT calculations for the catalytic cycle yield energy spans in agreement with the experimentally observed activity trend. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 126
页数:10
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