The tautomerism of 2-hydroxypyridinef2-pyridinone has been investigated by microwave spectroscopy using both a conventional spectrometer and also a jet-cooled millimeter-wave spectrometer. We have observed spectra attributable to both the (Z)-hydroxy tautomer and the pyridinone tautomer and also their monodeutero isotopomers, the relative abundances in both spectrometers being about 3:l in favor of the hydroxy form. From relative intensity and dipole moment measurements, we estimate the energy difference between the vibrational ground states of the two tautomers to be = 270 (30) cm-I. The rotational constants for 2-pyridinone yield an inertial defect that demonstrates the planarity of this tautomer, in contrast to recent reports of the nonplanarity of pyridinone. We can detect no lines that could be assigned to such a conformer. There are no lines correspondingto the E isomer of 2-hydroxypyridine, indicating that its relative abundance in the jet is less than -5% of the 2 isomer. The rotational spectra of several vibrational satellites have also been assigned. Identification of species is based on comparison of rotational constants determined experimentally with the values predicted from molecular orbital calculations and independently confirmed by comparison of observed and theoretically predicted hyperfine multiplets. The observed rotational constants for both tautomers are within 2% of thevalues predicted by ab initio molecular orbital calculations at the basis set level of 6-31G*, a degree of agreement similar to that found in some previous studies of nitrogen heterocycles. Nitrogen quadrupole coupling constants have been determined for both species: (Z)-2-hydroxypyridine, xOO = 0.4 (3) MHz, Xbb = -2.3 (3) MHz; 2-pyridinone, xcc = -2.8 (2) MHz. These values provide an independent confirmation of the identification of the two species of the molecule.

A shortening of the C-H bond lengths and a blue shift of the C-H stretching frequencies for the C-F small middle dot small middle dot small middle dotH-C groups indicates that anti-hydrogen bonds are present the difluoromethane dimer. The most stable conformer has three such interactions (shown schematically).

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The supersonic molecular beam (absorption millimeter wave and microwave Fourier transform) spectra of the 1:1 complex between pyrimidine and four isotopomers of water (H2O, HDO, D2O, and H2 18O) have been assigned. The derived moments of inertia are consistent with a planar (or nearly planar) structure of the adduct in which one hydrogen of the water molecule is bound to the nitrogen of the aromatic ring, and the “free” water hydrogen is entgegen to the ring. Only high level ab initio calculations (6-31G**+MP2-BSSE) account for the coplanarity of the water with the ring molecule. The hydrogen bond stretching force constant and the dissociation energy have been derived to be k s = 13.8 Nm-1 and Δ E = 21.4 kJ/mol, respectively.