Artículos de revistas
Conformational Analysis And Stereoelectronic Effects In Trans-1,2-dihalocyclohexanes: 1h Nmr And Theoretical Investigation.
Registro en:
Spectrochimica Acta. Part A, Molecular And Biomolecular Spectroscopy. v. 61, n. 8, p. 1771-6, 2005-Jun.
1386-1425
10.1016/j.saa.2004.07.007
15863046
Autor
Freitas, Matheus P
Rittner, Roberto
Tormena, Cláudio F
Abraham, Raymond J
Institución
Resumen
The conformational equilibrium of trans-1,2-difluoro- (1), trans-1,2-dichloro- (2) and trans-1,2-dibromo-cyclohexane (3) was studied through a combined method of NMR, theoretical calculations and solvation theory. The solvent dependence of the 3JH1,H2 NMR coupling constants together with theoretical calculations allow the direct determination of the conformational equilibria without recourse to model compounds. The coupling constants were obtained with the aid of spectrum simulation, since these symmetric molecules present complex coupling systems. The observed couplings, when analysed by solvation theory and utilising DFT geometries (B3LYP/6-311+G**), gave energy values of E(ee) -E(aa) of 0.10, 0.95 and 1.40 kcalmol(-1) in the vapour phase for 1, 2 and 3, respectively, decreasing to -0.63, 0.36 and 0.93 kcalmol(-1) in CCl4 and to -1.91, -0.80 and -0.05 kcalmol(-1) in DMSO solution. The diaxial preference for all compounds is explained by natural bond orbital (NBO) analysis, which shows important hyperconjugative effects in this conformation. The gauche effect for compounds with more electronegative substituents, which are in gauche arrangement in the ee conformation, also plays a relevant role in more polar solvents. 61 1771-6