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Suzuki coupling reactions in pure water catalyzed by supported palladium -relevance of the surface polarity of the support

  • RWTH Aachen University
  • Technical University of Munich

Research output: Contribution to journalArticlepeer-review

72 Scopus citations

Abstract

Heterogeneous (supported) palladium catalysts like palladium on carbon and a variety of metal oxides have been shown to be highly active for Suzuki coupling reactions in neat water under mild reaction conditions (T=65°C). It has been demonstrated for the first time that hydrophobic effects of the catalyst surface play an important role for the catalyst activity in water. Catalysts possessing hydrophobic surfaces (e.g., palladium on carbon) show higher activity for Suzuki coupling reactions in water than their hydrophilic counterparts (palladium on metal oxides). Tuning of the surface polarity of metal oxide supports (by silylation) results in higher activity under these conditions. Stronger alkaline conditions (three-fold excess of base) compensate the effect of hydrophobic supports and result in high activity of the catalysts also with hydrophilic supports. The addition of tetrabutylammonium bromide to generate, activate and stabilize the catalytic species (dissolved palladium complexes) is necessary for the conversion of more demanding substrates. The reaction is considered to be homogeneous taking place near the catalyst surface inside a droplet or layer of the reactant.

Original languageEnglish
Pages (from-to)767-775
Number of pages9
JournalAdvanced Synthesis and Catalysis
Volume353
Issue number5
DOIs
StatePublished - 28 Mar 2011

Keywords

  • Suzuki-Miyaura reaction
  • palladium
  • supported catalysts
  • water

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