A Combined Experimental and Theoretical Study Examining the Binding of N-Heterocyclic Carbenes (NHC) to the Cp*RuCl (Cp* = η5-C5Me5) Moiety: Insight into Stereoelectronic Differences between Unsaturated and Saturated NHC Ligands

Authors: Anna C. Hillier, William Sommer, Ben S. Yong, Jeffrey L. Petersen, Luigi Cavallo, Steven P. Nolan - Organometallics 2003 cited by 459

Combined solution calorimetric and quantum mechanics studies of reactions involving saturated and unsaturated N -heterocyclic carbene (NHC) ligands show that the difference in their relative bond dissociation energies is very small (1 kcal·mol - 1 ). Structural and computational studies reveal small metric parameter differences. These observations in conjunction with relative reactivity profiles of NHC-modified ruthenium-based olefin metathesis catalysts suggest that very small changes in the donor properties of the NHC ligands can translate into significant differences in catalytic properties.