AB Initio Study Of Bond Breaking In Olefins. GVB Computations On Propene Ã¯ÂÂ Methyl + Vinyl And Propene Ã¯ÂÂ H+Propen-2-YlAuthor(s): Y.Moussaoui, O.Ouamerali, George R.De Mare
The Generalized-Valence-Bond-Perfect-Pairing (GVB-PP) method is used to investigate the structural behaviour, energy, and dipole moment along the reaction coordinates for (1) propeneï®methyl+vinyl and for(2) propeneï®H+propen-2-yl. Geometry optimisations are carried out at the GVB(9)/STO-3G level (complete valence shell) for the minimum energy propene structure and for numerous structures up to r(C2-C3) and r(H3-C2)=10Aï°(only the elongated C2-C3 and C3-H2 distances are kept fixed, respectively). Both dissociation curves are smooth, without a maximum, and yield predicted dissociation energies for reaction(1) and (2) of 499.1 and 543.6 kJ.mol-1, respectively. (The latter value is about 10 kJ.mol-1 lower than those predicted for the primary ï¡(C-H) bond ruptures in propene, using the same method and basis set) GVB(7)/ 6-31G//GVB(9)/STO-3G computations lower the predicted dissociation energies for reactions(1) and (2) to 392.6 kJ.mol-1 and 435.7 kJ.mol-1, respectively. CCSD/cc-pVDZ calculations yield intermediate dissociation energies of 427.6 and 460.5 kJ.mol-1 for reactions(1) and (2), respectively. Linear behaviour is observed at long bond distances when the reduced energy concept, ER=(Er - E8)/De, is applied to the reaction coordinates.