ENTHALPIES OF REACTION OF CP'RU(COD)CL(CP'=C5H5,C(5)ME(5), COD EQUALSCYCLOOCTADIENE) WITH P(P-XC(6)H(4))(3) (X=CL, F, H, CH3, CF3,OCH3) LIGANDS - LIGAND STERIC VS ELECTRONIC CONTRIBUTIONS TO THE ENTHALPY OF REACTION
Sa. Serron et al., ENTHALPIES OF REACTION OF CP'RU(COD)CL(CP'=C5H5,C(5)ME(5), COD EQUALSCYCLOOCTADIENE) WITH P(P-XC(6)H(4))(3) (X=CL, F, H, CH3, CF3,OCH3) LIGANDS - LIGAND STERIC VS ELECTRONIC CONTRIBUTIONS TO THE ENTHALPY OF REACTION, Organometallics, 14(11), 1995, pp. 5290-5297
The enthalpies of reaction of Cp'Ru(COD)Cl (1; Cp' = eta(5)-C5H5, eta(
5)-C(5)Me(5); COD cyclooctadiene) with a series of para-substituted mo
nodentate tertiary phosphine ligands, leading to the formation of Cp'R
u(PR(3))(2)Cl, have been measured by anaerobic solution calorimetry in
THF at 30.0 degrees C. These reactions are rapid and quantitative. St
ructural studies have been carried out on three complexes in this seri
es. The relative importance of phosphine steric vs electronic ligand p
arameters is more closely examined in terms of the presented quantitat
ive thermochemical and structural information. Comparisons with enthal
py data in this and related organometallic systems are also presented.