Article ID Journal Published Year Pages File Type
9577793 Chemical Physics Letters 2005 7 Pages PDF
Abstract
Our results demonstrate that the equatorial C-H groups of 1,3-dioxane form hydrogen-bond-like C-H⋯O interactions more readily than do the axial C-H groups. The peak frequency of the strong axial C-H stretch band of 1,3-dioxane in a dilute D2O solution possesses an unusual non-monotonic pressure dependence, which indicates enhanced C-H⋯O hydrogen bond formation at high pressure. We performed density functional theory calculations to predict the relative energies and total interaction energies of 1,3-dioxane/(water)n clusters and found that the equatorial C-H groups are more favorable sites for hydrogen bonding than are the axial C-H groups.
Related Topics
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
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