A facile route to ruthenium-carbene complexes and their application in furfural hydrogenation

Authors
Publication date 2010
Journal Applied Organometallic Chemistry
Volume | Issue number 24 | 2
Pages (from-to) 142-146
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
Abstract
A number of new N-heterocyclic carbene (NHC) ligands were synthesized via a multicomponent reaction, wherein an aldehyde or ketone, a primary amine and an α-acidic isocyanide were reacted, giving the corresponding 2H-2-imidazolines. These were easily alkylated with an alkyl halide at position N-3, yielding the final NHC precursors, that were then complexed with Ru in situ. The resulting complexes are shown to be active and selective catalysts for the transfer hydrogenation of furfural to furfurol, using isopropanol as the hydrogen source. Importantly, the carbene ligand remains coordinated to the ruthenium center throughout the reaction.
Document type Article
Language English
Published at https://doi.org/10.1002/aoc.1584
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