ISSN:
0020-7608
Keywords:
Computational Chemistry and Molecular Modeling
;
Atomic, Molecular and Optical Physics
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
The direct dissociation of ethylene into two methylenes is studied along the least motion reaction path by means of an ab initio multiconfiguration self-consistent-field (MCSCF) calculation. All eight configurations arising from those valence orbitals that form the CC bonds, seven of them singlet coupled and one triplet coupled, are taken into account. The HCH bond angle is optimized along the entire reaction path. Separate MCSCF optimizations are carried through for the lowest two states of 1Ag symmetry. The (1Agσ2π2) ethylene ground state dissociates into two (3B1σπ) ground-state methylenes. The (1Agσ2π*2) excited state of ethylene dissociates into two (1A1σ2) excited methylenes. It is established that both these dissociations proceed without any barrier in the energy curve. In the ground state, where orbital symmetry is conserved, the π-bond breaks before the σ-bond, and the calculated heat of reaction agrees within 6 kcal/mol with the experimental value. In the excited state, where orbital symmetry is not conserved, the nonbonded repulsion between methylene σ2 lone pairs is found to blend into the antibonding character of the excited ethylene, yielding an energy curve that is everywhere repulsive. However, the variation of the HCH angle during the dissociation process is not simple, initially it expands and subsequently it contracts. Quantitative analytical approaches are developed which furnish conceptual interpretations of the orbital changes and configurational changes along the reaction path.
Additional Material:
13 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/qua.560160512
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