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The high-resolution infrared spectrum of CHD279Br has been investigated by Fourier transform spectroscopy in the range 540–615 cm−1 at an unapodised resolution of 0.0035 cm−1. This spectral region is characterised by the ν6 fundamental (584.8510 cm−1), corresponding to C–Br stretching mode, and its hot band 2ν6−ν6 (578.4333 cm−1). The spectral analysis resulted in the identification of 3430 transitions (J' ≤ 73 and K'a ≤ 18) for the ν6 fundamental and 1212 transitions (J' ≤ 49 and K'a ≤ 11) for the hot band 2ν6−ν6. The assigned data have been fitted using the Watson's S-reduced Hamiltonian in the Ir representation and new constants for the ground state from about 24,600 combination differences and sets of parameters for the v6 = 1 and 2 vibrational states have been obtained. From spectral simulations the intensity ratio between 2ν6−ν6 and ν6 has been estimated to be 0.15 ± 0.02. High-quality ab initio calculations have also been performed at the CCSD(T) level of theory in order to support the experimental investigation through the calculation of molecular parameters relevant to ro-vibrational spectroscopy. [ABSTRACT FROM AUTHOR]

The Fourier transform infrared (FTIR) spectrum of vinyl fluoride, H2C=CHF, has been widely investigated in the region of the ν4+ν7 combination band around 2800 cm−1 at a resolution of 0.005 cm−1. This vibration of A' symmetry gives rise to an a/b-hybrid band with a predominant a-type component. The rovibrational structure is strongly perturbed and the analysis has been rather complicated since this combination band is involved at least in a seven-level interacting polyad, including the ν8+2ν10, 2ν8+ν10, 2ν7+ν9, ν7+ν8+ν12, ν5+ν9+ν10 and ν7+ν10+ν12 vibrational states. The study has been further complicated by the absence of transitions coming from the perturbers that were considered as dark states. The spectral analysis resulted in the identification of 936 transitions with J" ≤ 46 and Ka" ≤ 11, all belonging to the a-type component. Most of the assigned data have been fitted using the Watson's A-reduction Hamiltonian in the Ir representation and proper Coriolis perturbation operators. The model employed includes seven different resonances within a complex polyad resonant system and a set of spectroscopic constants for the ν4+ν7 combination band, for the dark states, and Coriolis coupling coefficients have been determined. [ABSTRACT FROM AUTHOR]

The vibration-rotation spectrum of vinyl fluoride has been investigated in the nu4 band region around 1656 cm-1 at a resolution of about 0.003 cm-1 using a Fourier transform infrared spectrometer. This fundamental of symmetry species A' is mainly affected by first-order b-Coriolis resonance with the close-lying nu8 + nu12 and 2nu9 + nu12 levels. The rovibrational analysis led to the identification of about 2000 lines with J 58 and Ka 16 of the predominant a-type component. Using Watson's A-reduction Hamiltonian in the I r representation, a set of effective constants for the nu4 band was obtained employing transitions free of major resonance contribution. Even though no direct transitions to the perturbing levels have been observed, the determination of a few constants for the perturber nu8 + nu12 has been achieved. [ABSTRACT FROM AUTHOR]