High-resolution carbon-13 NMR spectra were obtained for three solid fl
uorinated steroids. Assignments were carried out using several approac
hes, including two-dimensional spectra of the compounds in solution. S
olid-state and solution-state chemical shifts are compared. Signals fr
om one of the fluorine-containing carbons in each compound show the ef
fect of interplay between shielding, dipolar and indirect scaler (J) c
oupling tensors. One sample is found to be a mixture of two polymorphi
c forms.