Transition dipole calculations, vibrational line

A number of researchers [15, 38 40, 43, 113, 124 126, 128, 146] have used mixed quantum/classical models, mostly as described in Section III.A, to calculate vibrational line shapes for this system, and several are in fair agreement with experiment. Here we describe our latest work involving approaches discussed in Section III.C. Our theoretical line shapes are calculated as briefly described in previous sections and in published work [98]. From an MD simulation of SPC/E heavy water, we determine the electric field on each putative H atom. We then use electric field maps to determine the transition frequency and dipole derivative. The orientational contribution to mp(t) we... 

We have described our most recent efforts to calculate vibrational line shapes for liquid water and its isotopic variants under ambient conditions, as well as to calculate ultrafast observables capable of shedding light on spectral diffusion dynamics, and we have endeavored to interpret line shapes and spectral diffusion in terms of hydrogen bonding in the liquid. Our approach uses conventional classical effective two-body simulation potentials, coupled with more sophisticated quantum chemistry-based techniques for obtaining transition frequencies, transition dipoles and polarizabilities, and intramolecular and intermolecular couplings. In addition, we have used the recently developed time-averaging approximation to calculate Raman and IR line shapes for H20 (which involves... 

First, as the molecule on which the chromophore sits rotates, this projection will change. Second, the magnitude of the transition dipole may depend on bath coordinates, which in analogy with gas-phase spectroscopy is called a non-Condon effect For water, as we will see, this latter dependence is very important [13, 14]. In principle there are off-diagonal terms in the Hamiltonian in this truncated two-state Hilbert space, which depend on the bath coordinates and which lead to vibrational energy relaxation [4]. In practice it is usually too difficult to treat both the spectral diffusion and vibrational relaxation problems at the same time, and so one usually adds the effects of this relaxation phenomenologically, and the lifetime 7j can either be calculated separately or determined from experiment. Within this approach the line shape can be written as [92 94]... 

To perform the VES calculations it is necessary to consider a finite duration pulse, which has a finite bandwidth. In addition, the actual shape of the vibrational echo spectrum depends on the bandwidth of the laser pulse and the spectroscopic line shape. Several species with different concentrations, transition dipole moments, line shapes, and homogeneous dephasing times can contribute to the signal. Therefore, VES calculations require determination of the nonlinear polarization using procedures that can accommodate these properties of real systems. 

Write a computer program to calculate the relative intensities of the spectral fines in the fundamental band of the vibration-rotation spectrum of a diatomic molecule, assuming that the absorbance is displayed in the spectrum. Set the maximum absorbance of the first line of the P branch equal to 1. Assume the Boltzmann probability distribution and assume that the transition dipole moments for all transitions are equal. Use your program to calculate the relative intensities for the first 15 lines in each branch of the HCl spectrum... 

RAIRS spectra contain absorption band structures related to electronic transitions and vibrations of the bulk, the surface, or adsorbed molecules. In reflectance spectroscopy the ahsorhance is usually determined hy calculating -log(Rs/Ro), where Rs represents the reflectance from the adsorhate-covered substrate and Rq is the reflectance from the bare substrate. For thin films with strong dipole oscillators, the Berre-man effect, which can lead to an additional feature in the reflectance spectrum, must also be considered (Sect. 4.9 Ellipsometry). The frequencies, intensities, full widths at half maximum, and band line-shapes in the absorption spectrum yield information about adsorption states, chemical environment, ordering effects, and vibrational coupling. 

An example of the resolution of this type of Stark spectroscopy is given in Fig. 6 at the fairly low electric field strength of 150 V/cm. Three Mp-components of the N = 3 - 2, J = 2.5 - 1.5, F = 5 - A transition in the X Z", y = 0 state of Cal near 12.3 GHz are well resolved in a 800 kHz mw scan. The electric field shifts were followed up to 900 V/cm and are depicted in Fig. 7. The measured data points lie well on the solid lines which represent the line positions calculated with the fitted dipole moment. The high accuracy of this method allowed the determination of the vibrational dependence of the electric dipole moment e.g. in the case of SrF. ... 

The contributions of the various intermolecular interactions to the vibrational coupling in Van der Waals complexes have been calculated explicitly for (SFe)25 (SiF4)2 and (81114)2. To try and simulate the dimer vibrational spectra (see Section 4) in the frequency range from 880 to 1100 cm , we have also calculated the infrared intensities of the dipole allowed transitions. We concentrate, in particular, on the dependence of the calculated spectra on the monomer orientations. In line with the atom-atom model used for the intermolecular potential, we write the following expression for the vibrational dipole moment operator of a dimer... 

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