Thermochemical data hydride complexes

This type of side-on bending, which has been established by X-ray crystallographic methods for the related acyl complexes (r 5-C5H5)2Zr(COMe)Me (38) and (T>5-C5H5)2Ti(COMe)Cl (39), could overcome the thermodynamic objection, previously discussed, against the formation of a normal, linearly bonded formyl by CO insertion into a metal-hydride bond. Thermochemical data obtained from alcoholysis of zirconium tetralkyl species show that the mean bond energy of Zr—O is 50 kcal/mole greater than that of Zr—C (40). 

The stepwise bond dissociation enthalpies Dj (Ti-Me) and D2(Ti-Me) in TiMe2Cp2 established from thermochemical data and extended Huckel calculations are compared to the respective halides and hydrides.34 The isolated C-H stretches of M(CH2D)2Cp2 (M = Ti, Zr, Hf) are lower than any other studied methyl complexes and the C-H bonds in the hafnium species are the longest and weakest yet characterised by this method.35... 

Eq. (8) requires determination of the two-electron oxidation potential of L M by electrochemical methods. When combined with the two-electron reduction of protons in Eq. (9), the sum provides Eq. (10), the AGh- values of which can be compared for a series of metal hydrides. Another way to determine the AGh-entails the thermochemical cycle is shown in Scheme 7.3. This method requires measurement of the K of Eq. (11) for a metal complex capable of heterolytic cleavage of H2, using a base (B), where the pK., of BH+ must be known in the solvent in which the other measurements are conducted. In several cases, Du-Bois et al. were able to demonstrate that the two methods gave the same results. The thermodynamic hydricity data (AGh- in CH3CN) for a series of metal hydrides are listed in Table 7.4. Transition metal hydrides exhibit a remarkably large range of thermodynamic hydricity, spanning some 30 kcal mol-1. 

M—H bond dissociation energies, 1, 287 photochemistry, 1, 251 single crystal neutron diffraction, 1, 578 stability toward disproportionation, 1, 301 Metal—hydrogen bonds bond dissociation energy in 1,2-dichloroethane, 1, 289 stable metal hydrides in acetonitrile, 1, 287 thermochemical cycle, 1, 286 in THF and dichloromethane, 1, 289 olefin insertion thermodynamics, 1, 629 in Zr(IV) bis-Cp complexes, 4, 878 Metal—hydrogen hydricity data, 1, 292... 

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