Search results for "Diatomic molecule"
showing 10 items of 86 documents
Analysis of the CIPSI/DCCI approach to characterize the HF AND F2 single bond
1990
Abstract The aim of the present work is to account for the main differential correlation contributions occurring during the bond breaking process of HF and F2 molecules in an accurate and inexpensive way. Starting from the dissociation-consistent configuration interaction (DCCI) scheme by Goddard and co-workers the corresponding contributions are evaluated within the framework reported by Malrieu and co-workers, namely configuration interaction by perturbation with multiconfigurational zeroth-order wavefunction selected by iterative process (CIPSI). In addition, the DCCI scheme has been improved by introducing the dispersion effects associated with the valence MOs adjacent to the bond. The …
Breather Molecular Complexes in a Passively Mode‐Locked Fiber Laser
2021
International audience; Breathing solitons are nonlinear waves in which the energy concentrates in a localized and oscillatory fashion. Similarly to stationary solitons, breathers in dissipative systems can form stable bound states displaying molecule-like dynamics, which are frequently called breather molecules. So far, the experimental observation of optical breather molecules and the real-time detection of their dynamics are limited to diatomic molecules, that is, bound states of only two breathers. In this work, the observation of different types of breather complexes in a mode-locked fiber laser: multibreather molecules, and molecular complexes originating from the binding of two breat…
Assessment for the mean value total dressing method: Comparison with coupled cluster including triples methods for BF, NO+, CN+, C2, BeO, NH3, CH2, H…
1997
Limited previous experience with the mean value total dressing (MVTD) method had shown that MVTD energies for closed shell systems are generally better than CCSD(T) ones compared to FCI. The method, previously published as total dressing 2′(td-2′), is based on the single reference intermediate Hamiltonian theory. It is not a CC method but deals in a great part with the same physical effects that CC methods that incorporate amplitudes of triples such as CCSDT or its CCSDT-1n approaches. A number of test calculations comparing to diverse CC methods, as well as FCI and experiment when available, have been performed. The tests concern equilibrium energies in NH3 and CH2, equilibrium energies an…
Fourier transform spectroscopy and direct potential fit of a shelflike state: application to E(4)1Σ(+) KCs.
2011
The paper presents high-resolution experimental study and a direct potential construction of a shelflike state E(4)(1)Σ(+) of the KCs molecule converging to K(4(2)S) + Cs(5(2)D) atomic limit; such data are of interest for selecting optical paths for producing and monitoring cold polar diatomics. The collisionally enhanced laser induced fluorescence (LIF) spectra corresponding to both spin-allowed E(4)(1)Σ(+) → X(1)(1)Σ(+) and spin-forbidden E(4)(1)Σ(+) → a(1)(3)Σ(+) transitions of KCs were recorded in visible region by Fourier transform spectrometer with resolution of 0.03 cm(-1). Overall about 1650 rovibronic term values of the E(4)(1)Σ(+) state of (39)K(133)Cs and (41)K(133)Cs isotopologu…
The chemical bonds in CuH, Cu2, NiH, and Ni2 studied with multiconfigurational second order perturbation theory
1994
The performance of multiconfigurational second order perturbation theory has been analyzed for the description of the bonding in CuH, Cu2, NiH, and Ni2. Large basis sets based on atomic natural orbitals (ANOS) were employed. The effects of enlarging the active space and including the core‐valence correlation contributions have also been analyzed. Spectroscopic constants have been computed for the corresponding ground state. The Ni2 molecule has been found to have a 0+g ground state with a computed dissociation energy of 2.10 eV, exp. 2.09 eV, and a bond distance of 2.23 Å. The dipole moments of NiH and CuH are computed to be 2.34 (exp. 2.4±0.1) and 2.66 D, respectively. pou@uv.es ; merchan@…
Collisional line broadening and line shifting in N2-CO2 mixture studied by inverse Raman spectroscopy
1990
Abstract Collisional effects in the Raman Q-branch of N 2 perturbed by CO 2 have been studied by high-resolution stimulated Raman spectroscopy. The Raman spectra recorded in the 0.3–1.0 atm and 295–1000 K pressure and temperature ranges are fitted with a theoretical profile taking into account line broadening, frequency shift and line mixing due to rotational energy transfers. The data at low density are used as basic data for the modeling of rotationally inelastic rates through sets of adjustable parameters. We have used in this study the two main models developed in the last decade and known as modified exponential gap (MEG) and energy corrected sudden (ECS) laws. Experimental spectra rec…
A MRCI PS and CASSCF study of the ground state MgO dissociation energy
1991
Abstract Ab initio calculations at CASSCF and MRCI PS levels are used to determine the dissociation energy for the X 1 Σ + state of MgO, which adiabatically dissociates to the ground state 1 S g of magnesium and to the excited 1 D g state of oxygen, as well as other spectroscopic parameters. Emphasis is placed upon the problem of properly selecting an adequate active space in CASSCF calculations and upon the improvements obtained in MRCI by selecting perturbatively the most important contributions to the total wavefunction and evaluating the remaining ones only by perturbational method. Through a procedure based on stabilizing the computed dissociation energy, values of 3.87 eV (MRCI PS) an…
A mutliconfigurational study of low-lying electronic states of KO
1992
Abstract Potential energy curves and spectroscopic parameters of several electronic states of the KO molecule have been calculated using multi-configurational methods. The KO B 2Π state, first time theoretically described, presents a strong avoided crossing with the A 2Π state, and allows for the explanation of the observed fluorescence of the KO molecule. Eleven electronic states have been studied at all the internuclear distances. Effects of complete active space and basis set selections on the results are also analyzed.
Theoretical spectroscopic parameters of the alkali monofluorides LiF, NaF and KF
1992
Abstract Multireference configuration interaction and second-order perturbation theory are used to determine accurate spectroscopic parameters for the ground state of the alkali monofluorides from LiF to KF. Systematic saturation of the spdf subspaces of the atomic basis sets for the electron affinity of fluorine and the ionization potential of the metals have been shown to be more efficient than for the approximate dissociation energies in the molecule. the calculated rotational and vibrational constants and transitions for the three systems show excellent agreement with the expeirmental data.
MCSCF determination of the KO molecule ground state.
1992
Abstract Ab initio calculations at the MC/CASSCF level are used to determine in an accurate way the nature and position of the ground state of the KO molecule. The characteristic 2 Π and 2 Σ + alkali monoxide ionic states show a theoretical energy separation of about 0.04 eV, which produces opposite results by authors in favour of one or the other symmetry. We test the basis set dependence and active space dependence of the calculated energetical ordering of both states, with an extensive study of the active orbitais selection; the results show a ground state of 2 Σ + symmetry.