Palladium leaching dependent on reaction parameters in Suzuki-Miyaura coupling reactions catalyzed by palladium supported on alumina under mild reaction conditions

被引:134
作者
Soomro, Saeeda S. [1 ]
Ansari, Farzana L. [2 ]
Chatziapostolou, Konstantinos [1 ]
Koehler, Klaus [1 ]
机构
[1] Tech Univ Munich, Dept Chem, D-85747 Garching, Germany
[2] Quaid i Azam Univ, Dept Organ Chem, Islamabad 45320, Pakistan
关键词
Suzuki-Miyaura couplings; Palladium leaching; Supported catalysts; Heterogeneous catalysis; HIGHLY-ACTIVE CATALYST; HETEROGENEOUS SUZUKI; ARYL CHLORIDES; ARYLBORONIC ACIDS; LIGAND-FREE; HECK REACTIONS; C-C; PD/C; NANOPARTICLES; CARBON;
D O I
10.1016/j.jcat.2010.05.007
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
Suzuki couplings of aryl bromides as well as activated aryl chlorides can be efficiently performed by palladium supported on alumina under mild reaction conditions (T=65 degrees C). The catalyst prepared by controlled precipitation of palladium hydroxide shows a high activity and represents a perfect and robust alternative to other complex and expensive preparation procedures. Palladium leaching in the Suzuki couplings by supported palladium catalysts has been investigated in detail for the first time for such mild reaction conditions. Catalytic activity is due to palladium species dissolved from the solid particles. The active palladium species in solution are re-deposited onto the support with the completion of the reaction. Catalytic activity correlates with the amount of palladium dissolved. Palladium leaching is a prerequisite for highly efficient catalysis in particular for more demanding substrates. Palladium leaching depends on a variety of parameters (temperature, solvent, base, substrates, and additives). Transmission electron microscopic investigations show that - depending on the parameters - the efficient palladium re-deposition process can leave the catalyst with an unchanged dispersion and particle size distribution after the reaction. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:138 / 146
页数:9
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