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N-heterocyclic carbenes, part 33. Combining stable NHC and chelating pyridinyl-alcoholato ligands: A ruthenium catalyst for applications at elevated temperatures

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60 Scopus citations

Abstract

Ruthenium alkylidene complexes bearing one NHC ligand and one chelating pyridinyl alcoholate ligand 6 are generated by exchange of a phosphine ligand. Two synthetic approaches are presented: reacting the NHC phosphine complex 5 with the chelating ligand or reacting the pyridinyl-alcohol-atophosphine complex 3 with a free NHC ligand. To evaluate the properties of 6 as metathesis catalysts, ROMP experiments with the strained olefin norbornene and the less strained cyclooctene were performed at different temperatures.

Original languageEnglish
Pages (from-to)666-670
Number of pages5
JournalAdvanced Synthesis and Catalysis
Volume344
Issue number6-7
DOIs
StatePublished - 2002

Keywords

  • Homogeneous catalysis
  • N-heterocyclic carbenes
  • Olefin metathesis
  • Pyridinyl alcoholates
  • Ruthenium

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