Bifunctional (Cyclopentadienone) Iron-Tricarbonyl Complexes: Synthesis, Computational Studies and Application in Reductive Amination

被引:111
作者
Moulin, Solenne [1 ]
Dentel, Helene [1 ]
Pagnoux-Ozherelyeva, Anastassiya [1 ]
Gaillard, Sylvain [1 ]
Poater, Albert [2 ]
Cavallo, Luigi [3 ]
Lohier, Jean-Francois [1 ]
Renaud, Jean-Luc [1 ]
机构
[1] Univ Caen Basse Normandie, Normandie Univ, CNRS, Lab Chim Mol & Thioorgan,UMR 6507, F-14050 Caen, France
[2] Univ Girona, IQCC, Dept Quim, Girona 17071, Catalonia, Spain
[3] King Abdullah Univ Sci & Technol, Phys Sci & Engn Div, KAUST Catalysis Ctr, Thuwal 239556900, Saudi Arabia
关键词
amination; catalysis; density functional calculations; hydrogenation; iron; ASYMMETRIC TRANSFER HYDROGENATION; METAL-DIENE COMPLEXES; CATALYST DEACTIVATION PATHWAYS; MEDIATED 2+2+1 CYCLOADDITIONS; CHIRAL TITANOCENE CATALYST; OPPENAUER-TYPE OXIDATION; LIGAND-EXCHANGE REACTION; TRANSITION-METAL; ORGANIC-SYNTHESIS; CARBONYL-COMPOUNDS;
D O I
10.1002/chem.201302432
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reductive amination under hydrogen pressure is a valuable process in organic chemistry to access amine derivatives from aldehydes or ketones. Knolker's complex has been shown to be an efficient iron catalyst in this reaction. To determine the influence of the substituents on the cyclopentadienone ancillary ligand, a series of modified Knolker's complexes was synthesised and fully characterised. These complexes were also transformed into their analogous acetonitrile iron-dicarbonyl complexes. Catalytic activities of these complexes were evaluated and compared in a model reaction. The scope of this reaction is also reported. For mechanistic insights, deuterium-labelling experiments and DFT calculations were undertaken and are also presented.
引用
收藏
页码:17881 / 17890
页数:10
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