Single Site Supported Cationic Rhodium(I) Complexes for the Selective Redox Isomerization of Allylic Alcohols

被引:23
|
作者
Sahoo, Suman [1 ,2 ]
Lundberg, Helena [1 ,3 ]
Eden, Mattias [4 ]
Ahlsten, Nanna [1 ,3 ]
Wan, Wei [1 ,2 ]
Zou, Xiaodong [1 ,2 ]
Martin-Matute, Belen [1 ,3 ]
机构
[1] Stockholm Univ, Berzelii Ctr EXSELENT Porous Mat, SE-10691 Stockholm, Sweden
[2] Stockholm Univ, Inorgan & Struct Chem Unit, Dept Mat & Environm Chem, SE-10691 Stockholm, Sweden
[3] Stockholm Univ, Dept Organ Chem, SE-10691 Stockholm, Sweden
[4] Stockholm Univ, Phys Chem Unit, Dept Mat & Environm Chem, SE-10691 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
aluminosilicates; heterogeneous catalysis; hydrogen bonds; immobilization; mesoporous materials; noncovalent interactions; TRANSITION-METAL-COMPLEXES; SOLID-STATE NMR; CARBONYL-COMPOUNDS; CATALYZED ISOMERIZATION; ENANTIOSELECTIVE HYDROGENATION; HETEROGENEOUS CATALYSIS; HOMOGENEOUS CATALYSTS; MESOPOROUS SILICA; MOLECULAR-SIEVES; AQUEOUS-MEDIA;
D O I
10.1002/cctc.201100321
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
The isomerization of allylic alcohols to carbonyl compounds by a heterogeneous rhodium complex is reported. Different silica material supports and catalyst/ligand systems were evaluated. The most efficient catalyst in terms of catalytic activity and stability was found to be a cationic rhodium(I) complex with sulfonated phosphine ligands anchored on a mesoporous aluminosilica AlSBA-15. The heterogeneous complex catalyzed the isomerization of a variety of allylic alcohols in excellent yields with very low catalyst loadings (0.5 mol?%). The catalyst could be recycled without significant loss of activity or selectivity. The optimized catalyst was characterized by N2 sorption, powder X-ray diffraction, transmission electron microscopy, as well as solution and solid-state nuclear magnetic resonance, and Fourier Transform infrared spectroscopies.
引用
收藏
页码:243 / 250
页数:8
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