The trans-isomer of formanilide studied by microwave Fourier transform spectroscopy*

The rotational spectra of the trans-isomer of formanilide was recorded by microwave Fourier transform spectroscopy. The rotational and centrifugal distorsion constants as well as the quadrupole coupling constants have been accurately determined. It is shown that the stable conformation corresponds to a planar structure. The energy barrier between this conformation and the less stable one (the amino group lies in a plane perpendicular to the phenyl ring) has been evaluated by ab initio calculations. q 2005 Elsevier B.V. All rights reserved.