| Literature DB >> 27219852 |
Mirza Cokoja1, Robert M Reich2, Michael E Wilhelm2, Marlene Kaposi2, Johannes Schäffer3, Danny S Morris4, Christian J Münchmeyer2, Michael H Anthofer2, Iulius I E Markovits2, Fritz E Kühn2, Wolfgang A Herrmann2, Andreas Jess3, Jason B Love4.
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.Entities:
Keywords: epoxidation; homogeneous catalysis; ionic liquids; solubility; two-phase catalysis
Mesh:
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Year: 2016 PMID: 27219852 DOI: 10.1002/cssc.201600373
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928