The Mechanism and Design of Asymmetric Co-Arctate Br+ (Mobius) Atom Transfers Between Alkenes. A Computational Study

Ab initio calculations at the correlated MP2 and B3LYP/pVTZ level reveal that a bromine cation transfer between two alkenes involves a symmetrically 4-coordinated species which is an energy minimum in the gas phase energy profile. Electron withdrawing and donating substituents on one alkene distort the position of the bromine respectively away from and towards the substituted alkene. Alkenes strained by incorporating a trans configuration into 6-8 membered rings preferentially bind the Br cation, an equilibrium which can be tuned by using a combination of substituents and strain. The classification of such an atom transfer as a concerted coarctate reaction is discussed. Original publication: Internet Journal of Chemistry [online computer file]
Volume: 4
Pages: No pp. given, Article No. 10
Journal
2001