N-Donor ligands based on bipyridine and ionic liquids: an efficient partnership to stabilize rhodium colloids. Focus on oxygen-containing compounds hydrogenation

被引:31
作者
Denicourt-Nowicki, Audrey [1 ,3 ]
Leger, Bastien [1 ,2 ,3 ,4 ,5 ]
Roucoux, Alain [1 ,3 ]
机构
[1] Ecole Natl Super Chim Rennes, CNRS, UMR 6226, F-35708 Rennes 7, France
[2] UCCS, UArtois, F-62300 Lens, France
[3] Univ Europeenne Bretagne, Rennes, France
[4] Univ Lille Nord France, F-59000 Lille, France
[5] CNRS, UMR 8181, F-75700 Paris, France
关键词
TRANSITION-METAL NANOPARTICLES; PALLADIUM NANOPARTICLES; SELECTIVE HYDROGENATION; RUTHENIUM NANOPARTICLES; CATALYTIC-HYDROGENATION; BIPHASIC HYDROGENATION; ARENE HYDROGENATION; GOLD NANOPARTICLES; COORDINATION MODES; PHASE-TRANSFER;
D O I
10.1039/c1cp20602h
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
Polynitrogen ligands and/in ionic liquids (ILs) are described as a pertinent tandem to efficiently stabilize rhodium nanoparticles (NPs) in the size range of 2.0 nm for catalytic applications. Several N-donor ligands based on bipyridine skeleton were used as extra protective agents in [BMI][PF6] and compared in the hydrogenation of functionalized aromatic compounds at 80 degrees C and under 40 bar H-2. The nature of the bipyridine derivative and its influence on the coordination mode on the particle surface were proposed to explain the observed different kinetic properties. The hydrogenation of various oxygen-containing arenes was investigated and original results were described in the reduction of anisole and cresols as model lignin compounds, providing a significant ratio of ketone derivatives. A first explanation based on possible reaction routes is proposed to justify the formed products.
引用
收藏
页码:13510 / 13517
页数:8
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