Chiral Ammonium-Capped Rhodium(0) Nanocatalysts: Synthesis, Characterization, and Advances in Asymmetric Hydrogenation in Neat Water

被引:30
作者
Bile, Elodie Guyonnet [1 ,2 ]
Cortelazzo-Polisini, Elodie [1 ,2 ]
Denicourt-Nowicki, Audrey [1 ,2 ]
Sassine, Rita [3 ]
Launay, Franck [3 ]
Roucoux, Alain [1 ,2 ]
机构
[1] Ecole Natl Super Chim Rennes, CNRS, UMR 6226, F-35708 Rennes 7, France
[2] Univ Europeenne Bretagne, Rennes, France
[3] UPMC, Equipe Etud Supports Poreux Act & Catalyse Enviro, Lab Reactivite Surface, UMR CNRS 7197, F-94200 Ivry, France
关键词
ammonium; chirality; hydrogenation; nanoparticles; surfactants; PROMISING CATALYTIC-SYSTEMS; DIASTEREOSELECTIVE HYDROGENATION; ENANTIOSELECTIVE HYDROGENATION; RUTHENIUM NANOPARTICLES; HETEROGENEOUS CATALYSTS; SUBSTITUTED AROMATICS; ARENE HYDROGENATION; PLATINUM CATALYSTS; SUPPORTED RHODIUM; ACID-DERIVATIVES;
D O I
10.1002/cssc.201100364
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Optically active amphiphilic compounds derived from N-methylephedrine, N-methylprolinol, or cinchona derivatives possessing bromide or chiral lactate counterions were efficiently used as protective agents for rhodium(0) nanoparticles. The full characterization of these surfactants and the obtained nanocatalysts was performed by means of different techniques. These spherical nanoparticles, with sizes between 0.82.5 nm depending on the stabilizer, were evaluated in the hydrogenation of model substrates in neat water as a green solvent. The rhodium catalysts showed relevant kinetic properties, but modest enantiomeric excess values of up to 13?% in the hydrogenation of ethyl pyruvate. They were also investigated in the hydrogenation of disubstituted arenes, such as m-methylanisole, providing interesting catalytic activities and a preferential cis selectivity of around 80?%; however, no asymmetric induction was observed.
引用
收藏
页码:91 / 101
页数:11
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