Electronic excitation quantum chemical calculations

The requirements for Raman resonance that must be fulfilled are the following (120,121) (a) total symmetry of the vibrations with respect to the absorbing center, and (b) same molecular deformation induced by the electronic and vibrational excitations. Quantum chemical calculations (41) of the vibrational frequencies and the electronic structure of shell-3 cluster models allowed the assignment of the main vibrational features, as shown in Fig. 7. The 1125 cm-1 band is unequivocally assigned to the symmetric stretching of the Ti04 tetrahedron. 

According to a large number of experimental studies, the most stable phologen-erated species in the lowest excited stales of conjugated chains are electron-hole pairs bound by Coulomb attraction and associated to a local deformation of the backbone, i.e., polaron-excilons [18]. A good insight into the properties of these species can be provided by quantum-chemical calculations our recent theoretical... 

Quantum-chemical calculations were carried out and correlated with experimental observations concerning the electronic absorption, emission, and excitation spectra of (5-phenyl-l,3,4-oxadiazol-2-yl)-7-hydroxycoumarin 15 <2000SAA1773>. 

The measurements were carried out using polarized-light from synchrotron radiation. The angle-resolved UPS spectra were recorded for specific directions of photon incidence, photon polarization, and electron exit, chosen in order to resolve the momentum dependence of the 7t-electron energy bands which could be observed in this experiment. Details are available elsewhere63. The UPS results are analysed not only with the help of the valence effective Hamiltonian (VEH) method, but also with the help of new quantum-chemical calculations based upon the excitation model method64. The full VEH band structure is shown in Fig. 7.32. 

The quantum chemical modeling is a very useful supplement to spectroscopic experimental methods for investigation of properties of point defects, however, until recently it was used mainly for calculations of vertical excitation energies. The modeling of structural transformation in excited electronic states is still a rather complicated task, which requires state-of-the-art quantum chemical calculations. In this chapter, we first describe theoretical methods applied in ab initio and vibronic theory calculations and then demonstrate their applications in theoretical studies of various point defects in silica and germania. 

Table 7.9. Quantum-chemical calculations of the energies (eV) of the lowest electron-excited states for silicon-centered radicals3...

Abstract This work describes the ultrafast processes preceding the photoinduced decarbonylation of the simple metal carbonyl complexes Cr(CO)6, Fe(CO)5, and Ni(CO)4. Models for their electronic structure are presented based on recent ab initio quantum chemical calculations and these models are used to describe initial excited-state dynamics leading to the expulsion of one CO ligand. Experimental support for the proposed excited-state dynamics is presented, as obtained from ultrafast pump-probe experiments using mass-selective detection, ultrafast electron diffraction, and luminescence studies. The results of some steady-state experiments are also presented where they support the proposed dynamic model. 

---