Jet-Cooled Phosphorescence Excitation Spectrum of the T 1 (n,π*) ← S 0 Transition of 4 H -Pyran-4-one.

The 4 H -pyran-4-one (4PN) molecule is a cyclic conjugated enone with spectroscopically accessible singlet and triplet (n,π*)excited states. Vibronic spectra of 4PN provide a stringent test of electronic-structure calculations, through comparison of predicted vs measured vibrational frequencies in the excited state. We report here the T 1 (n,π*) ← S 0 phosphorescence excitation spectrum of 4PN, recorded under the cooling conditions of a supersonic free-jet expansion. The jet cooling has eliminated congestion appearing in previous room-temperature measurements of the T 1 ← S 0 band system and has enabled us to determine precise fundamental frequencies for seven vibrational modes of the molecule in its T 1 (n,π*) state. We have also analyzed the rotational contour of the 0 0 0 band, obtaining experimental values for spin-spin and spin-rotation constants of the T 1 (n,π*) state. We used the experimental results to test predictions from two commonly used computational methods, equation-of-motion excitation energies with dynamical correlation incorporated at the level of coupled cluster singles doubles (EOM-EE-CCSD) and time-dependent density functional theory (TDDFT). We find that each method predicts harmonic frequencies within a few percent of observed fundamentals, for in-plane vibrational modes. However, for out-of-plane modes, each method has specific liabilities that result in frequency errors on the order of 20-30%. The calculations have helped to identify a perturbation from the T 2 (π,π*) state that leads to unexpected features observed in the T 1 (n,π*) ← S 0 origin band rotational contour.