Abstract
Modern valence-bond theory, in its spin-coupled form, is used to study the electronic structure of the transition structures in the Cope rearrangement. It is found that the transition structure described by a “chair” geometry with a “6-in-6” CASSCF/6-31G* wave function is clearly aromatic while the CASSCF/6-31G*“boat” transition structure corresponds more closely to two weakly interacting allyl radicals. Moreover, there is a striking resemblance between the CASSCF chair transition structure and the benzene molecule, arising from the modern valence-bond analysis in terms of Rumer spin functions. In agreement with previous works, dynamical correlated wave functions show shorter interallylic distances in the optimized transitions structures. The use of spin-coupled wave functions on the latter geometries results in diradical and aromatic character for the chair and boat transition structures, respectively.
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More From: Theoretical Chemistry Accounts: Theory, Computation, and Modeling (Theoretica Chimica Acta)
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