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Reaction of a bis(pentafulvene)titanium complex with an N-heterocyclic olefin: C-H-activation leads to resonance between a titanium vinyl and titanium alkylidene complex.

Malte FischerMatthew M D RoySascha HüllerMarc SchmidtmannRuediger Beckhaus
Published in: Dalton transactions (Cambridge, England : 2003) (2022)
The N-heterocyclic olefin (NHO) ImMe 4 CH 2 (2) (ImMe 4 CH 2 = (MeCNMe) 2 CCH 2 ) was employed for the synthesis of the titanium complex 3 derived from an NHO ligand precursor. By reacting 2 with the bis(π-η 5 :σ-η 1 -pentafulvene)titanium complex 1a, the terminal ylidic methylene unit of 2 is deprotonated by the quaternary exocyclic carbon atom of one pentafulvene ligand of 1a yielding the titanium complex 3 which bears an anionic NHO ligand (ImMe 4 CH - ). 3 was characterized by NMR spectroscopy, single crystal X-ray diffraction and quantum chemical calculations. The latter highlight that 3 is best described as a titanium vinyl complex with significant contribution of the titanium alkylidene resonance structure.
Keyphrases
  • room temperature
  • molecular dynamics
  • ionic liquid
  • energy transfer
  • high resolution
  • magnetic resonance imaging
  • molecular dynamics simulations
  • magnetic resonance
  • quantum dots