Parity-violation effects in the vibrational spectra of CHFClBr and CDFClBr

Relativistic four-component electronic structure calculations at the density functional level have been carried out to describe parity-violation (PV) energy shifts to the total electronic energy for the chiral molecule CHFClBr. An n-mode (n = 3, 4) expansion of the complete potential energy surface at the explicitly correlated coupled-cluster level has been used for the vibrational analysis of PV effects for CHFClBr and CDFClBr. The vibrational spectrum and corresponding absolute intensities for fundamental, overtone, and combination band transitions obtained from a variational configuration interaction treatment are in excellent agreement with experimental data and the most accurate so far obtained. The results show that a 3-mode expansion is sufficient for the vibrational analysis. The PV energy shifts for the fundamental, overtone, and combination bands are all in the mHz region. The data provided will be useful for future detection of PV in chiral molecules.

Automated summary

Relativistic four-component electronic structure calculations were performed at the density functional level to analyze parity-violation (PV) energy shifts and vibrational effects in the chiral molecule CHFClBr. The results indicate that a 3-mode expansion is sufficient for vibrational analysis.