UC Pd: A New Form of Pd/C for Sonogashira Couplings

被引:24
作者
Duplais, Christophe [1 ]
Forman, Arnold J. [1 ]
Baker, Benjamin A. [1 ]
Lipshutz, Bruce H. [1 ]
机构
[1] Univ Calif Santa Barbara, Santa Barbara, CA 93106 USA
关键词
cross-coupling; green chemistry; heterogeneous catalysis; palladium; Sonogashira couplings; HECK REACTIONS; LIGAND-FREE; ARYL HALIDES; COPPER-FREE; ARYLDIAZONIUM SALTS; EFFICIENT SYNTHESIS; PALLADIUM; CATALYST; CARBON; SUZUKI;
D O I
10.1002/chem.200902471
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Screening of different sources of Pd/C shows reagents of highly variable nanoparticle sizes and oxidation states of the metal. Typically, catalysts with higher surface area are viewed as likely to be the more reactive. In this paper a new form of Pd/C, "UC Pd" is described that is shown to contain larger nanoparticles yet it is the most reactive catalyst of those sold commercially for Sonogashira coupling reactions. UC Pd functions efficiently in the absence of a copper co-catalyst, under very mild and "green" conditions using inexpensive 95% EtOH at 50 degrees C. It is also the only form of Pd/C that can be recycled. In side-by-side reactions with several commercially available forms of Pd/C, none compete successfully with UC Pd under standardized conditions. Physical data obtained from extensive surface analysis using TEM, XRD, XPS, and CO-TPD measurements lead to an explanation behind the unique reactivity of this new recyclable form of Pd/C.
引用
收藏
页码:3366 / 3371
页数:6
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