화학공학소재연구정보센터
Journal of the American Chemical Society, Vol.129, No.51, 15774-15774, 2007
An electronic rationale for observed initiation rates in ruthenium-mediated olefin metathesis: Charge donation in phosphine and N-heterocyclic carbene ligands
Ru K-edge XAS data indicate that second generation ruthenium-based olefin metathesis precatalysts (L = N-heterocyclic carbene) possess a more electron-deficient metal center than in the corresponding first generation species (L = tricyclohexylphosphine). This surprising effect is also observed from DFT calculations and provides a simple rationale for the slow phosphine dissociation kinetics previously noted for second-generation metathesis precatalysts.