An intramolecular bifurcated H-bond from the axial HO-2 group to the axial F-4 atom and to the O5 atom of α-D-hexopyranosides in apolar solvents is evidenced in (1)H NMR spectra. The H-accepting properties of the F atom are modulated by the orientation of the O-substituent at the C3 atom and by an additional F atom at the C4 atom.
Keywords:
carbohydrates
,density functional calculations
,fluorinated alcohols
,hydrogen bonds
,scalar couplings
,Carbohydrates
,Hydrocarbons, Fluorinated
,Hydrogen Bonding
,Models, Molecular
,Molecular Structure
,Pyrans