An Attempt for the Quantitative DFT-based Interpretation of the Conformational Preference of Negative Hyperconjugative Anomeric Effects in Trans-2,3- and Trans-2,5-dihalo-1,4-dioxanes
Journal: Chemical Methodologies (Vol.4, No. 3)Publication Date: 2020-05-01
Authors : Elahe Faramarzi; Reza Ghiasi; Masumeh Abdoli-Senejani;
Page : 311-323
Keywords : 1; 4-Dioxane; negative hyperconjugative effect; conformers; natural bond orbital analysis; electron deformation density;
Abstract
In this study, the stabilities of trans-2,3- and trans-2,5-dihalo-1,4-dioxanes conformers were investigated at the LC-BLYP/6-311+G(d,p) theory level. The total energies and dipole moments of the axial and equatorial conformations were calculated for the mentioned molecules. The stability of theconformers, bond distances and spin-spin coupling constants of C-Hax and C-Heq bonds were explained with the negative hyperconjugative anomeric effects. The negative hyperconjugative anomeric effects on these conformers were illustrated using the natural bond orbital (NBO) analysis. Deformation maps of electron density for these conformers were provided, as well. In the basis of these calculations, the axial conformer was more stable than equatorial conformer in the studied molecules. Moreover, the trans-2,3- and trans-2,5-dihalo-1,4-dioxanes molecules were iso-energetic.
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