Search results for "Transition dipole moment"
showing 10 items of 52 documents
Manipulation of Atoms and Molecules with Laser Radiation and External Fields
2006
The paper provides analysis of a process, when a laser radiation absorption of a specific polarization creates a specific spatial distribution of molecular bonds and angular momenta of small molecules. It is discussed how an external fields electric or magnetic can influence this distribution. Some practical examples involving optical polarization of molecules in magnetic and electric fields are presented.1
On the magnetic dipole moment of the153Tb ground state
1981
Temperature dependence of the angular distribution anisotropy of the 212·0 keV gamma-ray following the decay of153Tb oriented in a gadolinium host was measured at temperatures from 16 to 70 mK. Magnetic dipole hyperfine splitting parameter a0 for153Tb(Gd) and magnetic dipole moment of the153Tb ground state were estimated to be ¦a0¦≧1·2×10−5 eV and ¦μ¦≧≧3·1 nuclear magnetons, respectively.
Development of the Dipole Moment and Polarizability Operators of Octahedral Molecules
1999
We present a development of the dipole moment and polarizability operators of octahedral molecules, using a tensorial formalism analogous to the one developed for tetrahedral molecules. These operators are involved in the calculation of the intensities of rovibrational transitions as well as in the calculation of the Stark effect. Expressions for the matrix elements are derived. Two simplified models for the study of the Stark effect in such molecules are also proposed and discussed. Copyright 1999 Academic Press.
A Tensorial Formalism Adapted to the Rovibronic Couplings in the Colored Hexafluorides: Application to the nu(5)(F(2g)) and nu(3)(F(1u)) Modes.
2000
A tensorial formalism adapted to the case of transition-metal hexafluorides in a degenerate electronic state has been developed on the basis of preceding works about spherical-top molecules in a nondegenerate electronic state. We have introduced electronic operators constructed using group theory features and some physical considerations. Vibronic couplings (Jahn-Teller effect, etc.) have been reviewed for the triply degenerate vibrational modes nu(5)(F(2g)) and nu(3)(F(1u)) leading to the identification of the main vibronic parameters. For the first time, an effective rovibronic Hamiltonian as well as the effective transition moment operators (dipole moment and polarizability) for rovibron…
Quasirelativistic transition property calculations by the intermediate Hamiltonian method: Electronic transition dipole moments and radiative lifetim…
2001
We present a quasirelativistic method of ab initio calculations on molecular excited states and electronic transition moments within the relativistic effective potential approximation, based on the construction of intermediate Hamiltonians and spin-free one-particle transition density matrices by means of the many-body multipartitioning perturbation theory. The method is applied to describe the electronic transitions involved in the radiative decay of the ${A0}_{u}^{+},$ ${B0}_{u}^{+},$ and ${B1}_{u}$ states of ${\mathrm{Te}}_{2}.$ Good agreement of the computed transition dipole moment functions with their empirical counterparts is achieved. Theoretical radiative lifetime estimates for sev…
Dipole moments of aminophthalimides in the ground and excited electronic states
1995
Measurement of the Dipole Polarizability of the Unstable Neutron-Rich NucleusNi68
2013
The E1 strength distribution in Ni68 has been investigated using Coulomb excitation in inverse kinematics at the RB3-LAND setup and by measuring the invariant mass in the one- and two-neutron decay channels. The giant dipole resonance and a low-lying peak (pygmy dipole resonance) have been observed at 17.1(2) and 9.55(17) MeV, respectively. The measured dipole polarizability is compared to relativistic random phase approximation calculations yielding a neutron-skin thickness of 0.17(2) fm. A method and analysis applicable to neutron-rich nuclei has been developed, allowing for a precise determination of neutron skins in nuclei as a function of neutron excess.
Calculated rJ2-type effective dipole moment parameters for fundamental bands of tetrahedral XY4 molecules
1991
Abstract Formulas in terms of basic molecular constants are presented for effective dipole moment parameters which are responsible for second-order corrections to the line intensities of fundamental bands of tetrahedral XY 4 molecules. Two cases have been considered. In the first case all bands were considered as separate bands. In the second case the ν 2 and ν 4 bands were considered as interacting bands. The influence of effective Hamiltonian transformations on effective dipole moment parameters has been studied. Numerical calculations of effective dipole moment parameters for the ν 2 and ν 4 bands of 12 CH 4 have been performed. There is reasonable agreement between calculated and fitted…
top data system (TDS) software for spectrum simulation of asymmetric molecules
2005
Abstract The D 2 h TDS ( D 2 h Top Data System) program suite has been developed with the aim of studying any rovibrational band or polyad of X 2 Y 4 ( D 2 h ) asymmetric top molecules. It is based on the same principles as similar programs from our group already released for various molecular symmetries ( T d , O h , C 4 v , C 2 v ). We work in the O ( 3 ) ⊃ D 2 h chain and this choice has consequences on the method used to specify the input parameters of the programs for Hamiltonian and transition moment calculations. Two examples concerning the ν 12 and ν 2 bands of the C 2 H 4 molecule are presented. This suite consists of a series of FORTRAN programs called by a script. The whole packa…
Spectroscopy of X2Y4 (D2h) molecules: tensorial formalism adapted to the O(3)⊃D2h chain, Hamiltonian and transition moment operators
2003
Abstract A tensorial formalism adapted to the case of the X2Y4 molecules with D2h symmetry has been developed in the same way as in the previous works on XY4 (Td) and XY6 (Oh) spherical tops and XY5Z (C4v) symmetric tops. Here, we use the O(3)⊃D2h group chain. All the coupling coefficients and formulas for the computation of matrix elements are given for this chain and used in the case of the Hamiltonian and transition moment operators.