FT-spectroscopy of the CO rare isotopologue and deperturbation analysis of the AΠ(v = 3) level.

Research on CO was carried out using two complementary Fourier-transform methods: (1) vacuum-ultraviolet absorption spectroscopy, with an accuracy ca. 0.03 cm on the DESIRS beamline (SOLEIL synchrotron) and (2) visible emission spectroscopy with an accuracy of about 0.

VUV-VIS FT spectroscopy of the rare CO isotopologue of carbon monoxide: Analysis of the AΠ(v = 1) multiply-perturbed level.

Ro-vibronic spectra of the CO carbon monoxide isotopologue were obtained with (i) emission spectroscopy in the visible region using a Bruker IFS 125HR spectrometer (University of Rzeszów) and (ii) vacuum-ultraviolet absorption spectroscopy using the wave-front-division spectrometer on the DESIRS beamline of the SOLEIL synchrotron. A deperturbation analysis of the CO AΠ(v = 1) level was conducted from 598 observed transitions from the BΣ - AΠ(0, 1), CΣ - AΠ(0, 1), AΠ - XΣ(1, 0), BΣ - XΣ(0, 0), CΣ - XΣ(0, 0), IΣ - XΣ(2, 0) bands and five further nominally forbidden bands. An effective Hamiltonian and term-value fitting analysis was implemented.

Quantitatively Adequate Calculations of the H-Chelate Ring Distortion upon the S → S(ππ*) Excitation in Internally H-Bonded o-Anthranilic Acid: CC2 Coupled-Cluster versus TDDFT.

The S → S(π → π*) excitation in o-aminobenzoic acid causes strengthening of the N-H···O intramolecular hydrogen bond. The interplay of the hydrogen bond shortening, the hydrogen atom dislocation along the hydrogen bond, and the skeletal relaxation is investigated. These effects often cause the appearance of dual fluorescence from the π-conjugated internally H-bonded molecules, which is traditionally interpreted as the evidence of the excited-state intramolecular proton transfer process: ESPIT.

First analysis of the 1-v″ progression of the Ångström (B1Σ+-A1Π) band system in the rare 13C17O isotopologue.

The 1-v″ progression of the Ångström band system, so far unobserved in the rare (13)C(17)O isotopologue, was obtained under high resolution as an emission spectrum using a high accuracy dispersive optical spectroscopy. In the studied region 22,700-24,500 cm(-1), 146 spectral lines were observed, among which 118 were interpreted as belonging to the 1-0 and 1-1 bands of B-A system, and the next 28 were interpreted as extra lines belonging to the 1-1 band of B(1)Σ(+)-e(3)Σ(-) intercombination system, also unobserved in the (13)C(17)O molecule so far. All those lines were precisely measured with an estimated accuracy better than 0.

First spectroscopic studies of the B2Sigma+ --> X2Sigma+ system in the 12C17O+ molecule spectrum.

The emission spectrum of the B2Sigma+ --> X2Sigma+ system in the 12C17O+ has been recorded at high resolution with conventional spectroscopic techniques. A graphite hollow cathode lamp filled with oxygen, enriched approximately 45% with the 17O2 isotope, has given strong spectra of hitherto unreported bands system of 12C17O+. Four bands, which form the 0-v('') (v('')=1 -4) progression, have been rotationally analysed with effective Hamiltonians of Brown [J.