Olefin Epoxidation in Aqueous Phase Using Ionic-Liquid Catalysts

Mirza Cokoja, Robert M. Reich, Michael E. Wilhelm, Marlene Kaposi, Johannes Schäffer, Danny S. Morris, Christian J. Münchmeyer, Michael H. Anthofer, Iulius I.E. Markovits, Fritz E. Kühn, Wolfgang A. Herrmann, Andreas Jess, Jason B. Love

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Hydrophobic imidazolium-based ionic liquids (IL) act as catalysts for the epoxidation of unfunctionalized olefins in water using hydrogen peroxide as oxidant. Although the catalysts are insoluble in both the substrate and in water, surprisingly, they are very well soluble in aqueous H2 O2 solution, owing to perrhenate-H2 O2 interactions. Even more remarkably, the presence of the catalyst also boosts the solubility of substrate in water. This effect is crucially dependent on the cation design. Hence, the imidazolium perrhenates enable both the transfer of hydrophobic substrate into the aqueous phase, and serve as actual catalysts, which is unprecedented. At the end of the reaction and in absence of H2 O2 the IL catalyst forms a third phase next to the lipophilic product and water and can easily be recycled.

Original languageEnglish
Pages (from-to)1773-1776
Number of pages4
JournalChemSusChem
Volume9
Issue number14
DOIs
StatePublished - 21 Jul 2016

Keywords

  • epoxidation
  • homogeneous catalysis
  • ionic liquids
  • solubility
  • two-phase catalysis

Fingerprint

Dive into the research topics of 'Olefin Epoxidation in Aqueous Phase Using Ionic-Liquid Catalysts'. Together they form a unique fingerprint.

Cite this