Study on spectroscopic parameters and molecular constants of HCl(X^1Σ^+) molecule by using multireference configuration interaction approach

Equilibrium internuclear separations, harmonic frequencies and potential energy curves （PECs） of HCI（X1∑＋） molecule are investigated by using the highly accurate valence internally contracted multireference configuration interaction （MRCI） approach in combination with a series of correlation-consistent basis sets in the valence range. The PECs are all fitted to the Murrell-Sorbie function, and they are used to accurately derive the spectroscopic parameters （De, Do, ωeXe, αe and Be） Compared with the available measurements, the PEC obtained at the basis set, aug-cc-pV5Z, is selected to investigate the vibrational manifolds. The constants Do, De, Re, We, ωeXe, Ore and Be at this basis set are 4.4006 eV, 4.5845 eV, 0.12757 rim, 2993.33 cm^-1, 52.6273 cm^-1, 0.2981 cm^-1 and 10.5841 cm^-1, respectively, which almost perfectly conform to the available experimental results. With the potential determined at the MRCI/aug-cc-pV5Z level of theory, by numerically solving the radial Schrodinger equation of nuclear motion in the adiabatic approximation, a total of 21 vibrational levels are predicted. Complete vibrational levels, classical turning points, inertial rotation and centrifugal distortion constants are reproduced, which are in excellent agreement with the available Rydberg-Klein-Rees data. Most of these theoretical vibrational manifolds are reported for the first time to the best of our knowledge.

Ro-vibrational Spectra of the Simplest Deuterated Criegee Intermediate CD2OO

Criegee intermediates are of signi cance in the atmospheric chemistry.In this work,the rovibrational spectra of the simplest deuterated Criegee intermediate,CD2OO,were studied by a vibrational self-consistent eld/virtual con guration interaction(VSCF/VCI)method based on a nine-dimensional accurate potential energy surface and dipole surface for its ground electronic state.The calculated fundamental vibrational frequencies and rotational constants are in excellent agreement with the available experimental results.These data are useful for further spectroscopic studies of CD2OO.Especially,the rotational constants for excited vibrational levels are essential for experimental spectral assignments.However,the infrared intensities from di erent resources,including the current computation,the experiment,and previous calculations at the NEVPT2 and B3LYP levels,deviate signi cantly.

Spectroscopic investigations on NO^+(X^1Σ^+, a^3Σ^+, A^1Π) ion using multi-reference configuration interaction method and correlation-consistent sextuple basis set augmented with diffuse functions

Three low-lying electronic states （X1∑, a3∑＋, and A1II） of NO＋ ion are studied using the complete active space self-consistent-field （CASSCF） method followed by highly accurate valence internally contracted multi-reference configuration interaction （MRCI） approach in combination of the correlation-consistent sextuple basis set augmented with diffuse functions, aug-cc-pV6Z. The potential energy curves （PECs） of the NO＋（X1∑＋, a3∑＋, A1II） are calculated. Based on the PECs, the spectroscopic parameters Re, De, We, WeXe, ae, Be, and D0 are reproduced, which are in excellent agreement with the available measurements. By numerically solving the radial SchrSdinger equation of nuclear motion using the Numerov method, the first 20 vibrational levels, inertial rotation and centrifugal distortion constants of NO＋（X1∑＋, a3∑＋, A1II） ion are derived when the rotational quantum number J is equal to zero （J = 0） for the first time, which accord well with the available measurements. Finally, the analytical potential energy functions of these states are fitted, which are used to accurately derive the first 20 classical turning points when J = 0. These results are compared in detail with those of previous investigations reported in the literature.

Investigations on analytic potential energy function, spectroscopic parameters and vibrational manifolds (J = 0) of the SD + (X^3 Σ^- ) ion

This paper investigates the spectroscopic properties of the SD^＋（X^3∑^-） ion by employing the coupled-cluster singles-doubles-approximate-triples [CCSD（T）] theory combining with the quintuple correlation-consistent basis set augmented with diffuse functions （aug-cc-pV5Z） of Dunning and co-workers. The accurate adiabatic potential energy function is obtained by the least-squares fitting method with the 100 ab initio points, which are calculated at the unrestricted CCSD（T）/aug-cc-pV5Z level of theory over the internuclear separation range from 0.09 to 2.46 nm. Using the potential, it accurately determines the spectroscopic parameters （De, ωeХe, αe and Be）. The present De, Re, We, ωeХe, αe and Be results are of 3.69119 eV, 0.13644 nm, 1834.949 cm^-1, 25.6208 cm^-1, 0.1068 cm^-1 and 4.7778 cm^-1, respectively, which are in remarkably good agreement with the experimental findings. A total of 29 vibrational states has been predicted by numerically solving the radial Schrodinger equation of nuclear motion when the rotational quantum number J equals zero. The complete vibrational levels, classical turning points, inertial rotation and centrifugal distortion constants are reported when J = 0 for the first time, which are in good accord with the measurements wherever available.

Application of Lie algebraic method to the calculation of rotational spectra for linear triatomic molecules

The Hamiltonian describing rotational spectra of linear triatomic molecules has been derived by using the dynamical Lie algebra of symmetry group U1(4) U2(4). After rovibrationalinteractions being considered, the eigenvalue expression of the Hamiltonian has the form of term value equation commonly used in spectrum analysis. The molecular rotational constants can be obtained by using the expression and fitting it to the observed lines. As an example, the rotational levels of v2 band for transition (02°0-0110) of molecules N2O and HCN have been fitted and the fitting root-mean-square errors (RMS) are 0.00001 and 0.0014 cm-1, respectively.

Molecular mechanism of effect of rotating constant magnetic field on organisms

The effect of RCMF-magnetic therapy apparatus on signal substances was studied. The radioimmunoassay (RIA) suggested that the magnetic field increased β-endorphin markedly in plasma. ELISA indicated that the magnetic field inhibited vomiting reaction induced by chemotherapy drug, with reversible decrease of serotonin (5-HT) level in brains, small intestine tissue and serum. Furthermore, the bioeffect of magnetic fields on 5-HT level presented a typical window effect and post-effect, and the inhibitory effect of magnetic field on the emesis was parallel to the decrease level of 5-HT. This result implied that the decrease of 5-HT might be the basis of rotating constant magnetic field (RCMF) inhibiting drug-induced emesis. The nitric acid reductase-spectrophotometry and nicotinamide adenine dinucleotide-diaphorase/arginine-vasopressin (AVP) cytochemistry technique showed that the magnetic field induced nitric oxide (NO) increase in hypothalamus and the high NO(A) level lasted for 3 hours. The results suggested that NO(A) increases after the treatment of the magnetic field in hypothalamus, which may result from strong expression of NO-ergic neuron in paraventricular hypothalamic nucleus (PVN), periventricular hypothalamic nucleus (PEN) and supraoptic nucleus (SON). The coexistence of NO and AVP may play an important role in the regulation of endocrine and neuroendocrine by the magnetic field. And our data also confirmed that the magnetic field increased the content of NO so strongly that high NO level lasted for 3 hours, also made neuropeptide Y (NPY) cell in medulla stained heavily.

Hyperspherical Study of Ne_2Kr and Ne_2Xe Systems

We have calculated the ground state energies and rotational constants for the Ne2 Kr and Ne2 Xe systems, as well as their corresponding isotopes using the hyperspherical method. We used B-splines as basis function to expand channel functions and make the knot distribution of B-splines characterize the behavior of the channel function precisely. As a result, the extremely slow convergence of quantum mechanic calculation for these van der Waals trimers containing heavy element is improved greatly. The convergent rotational constants and the isotope shifts are obtained and compared with other theoretical and experimental values. Our results using newly proposed Tang-Toennies （TT） pair-wise potentials are consistent with that of Ernesti and Hutson’s calculation using HFD-B potentials, and give an improved agreement with experimental data.