Search results for "EXCITATION"
showing 10 items of 1290 documents
<title>Coumarin fluorescent probes by electro-optical and laser spectrofluorimetry methods</title>
1997
Modified electro-optical absorption and emission methods were used to measure the dipole moments of six coumarin fluorescent probes (CU1, CU4, CU7, CU30, CU120, CU334) in the equilibrated ground, excited Franck-Condon and equilibrated excited states. The measurements were performed in cyclohexane and dioxane at room temperature. The equilibrated ground and excited states dipole measured by electro-optical methods are compared with those derived from other measurements techniques and from semiempirical calculations. Experiments and calculations performed in this work reveal a set of anomalous and interesting properties of CU7 and CU30 in solutions. The spectral dependence of some electro-opt…
Elongated push–pull diphenylpolyenes for nonlinear optics: molecular engineering of quadratic and cubic optical nonlinearities via tuning of intramol…
1999
Abstract Push–pull polyenes are of particular interest for nonlinear optics (NLO) as well as model compounds for long-distance intramolecular charge transfer (ICT). In order to tune the ICT phenomenon and control the linear and nonlinear optical properties, we have synthesized and investigated several series of soluble push–pull diphenylpolyenes of increasing length and having various donor (D) and acceptor (A) end groups. Their linear and NLO properties have been studied by performing electro-optical absorption measurements (EOAM) and third-harmonic generation (THG) experiments in solution. Each push–pull molecule exhibits an intense ICT absorption band in the visible characterized by an i…
All-experimental values of self-quenching cross-sections for nf states (n=5-8) of potassium atoms
2007
All-experimental self-quenching cross-sections σ nf are reported for K(nf) states (n = 5, 6, 7, 8). The experiment was performed at varied temperatures of K vapour in a spectral cell. Time-resolved fluorescence was observed following pulsed step-wise excitation with dipole and quadrupole transitions K(4s) → K(4p) → K(nf). The values: σ 5f = 2.4 ± 1.7, σ 6f = 4.5±1.4, σ 7f = 8.1±1.8, and σ 8f = 18.2±3.0 (in units of 10−13 cm−1) were obtained from a Stern-Volmer-type plot.
Use of the red-edge excitation effect for investigation of dielectric interactions in biomembranes
1999
Dipole moments of the fluorescent probes 1-phenylnaphthylamine (1-AN) and 1-anilinonaphthalene-8-sulfonate (1,8-ANS) are measured using electro-optical absorption and emission methods. Dipole moments in the ground and excited states were measured in cyclohexane and dioxane. It is shown that the charge distributions in the 1-AN and 1,8-ANS molecules differ substantially. The spectral dependence of the electro-optical coefficients suggests that the absorption spectrum of 1,8-ANS is due to a superposition of (at least two) electronic transitions. It is found that spectra of 1-AN in erythocyte ghosts are inhomogeneously broadened. The above effect makes it possible to selectively excite probe m…
A Theoretical Study of the Electronic Spectra of N9 and N7 Purine Tautomers
1999
The complete active space (CAS) SCF method and multiconfigurational second-order perturbation theory (CASPT2) have been used to study electronic spectra of the N(9)H and N(7)H tautomers of purine. The calculations include vertical excitation energies, oscillator strengths, dipole moments, and transition moment directions in gas phase. In accord with experiment in nonpolar solvents, the two lowest π → π* excited singlet valence states are predicted to be located at 4.7 and 5.1 eV. The latter is expected to shift to the red in aqueous solutions. A satisfactory interpretation of the electronic spectra above 5.5 eV is obtained if the experimental data are assumed to consist of the superposition…
Calculation of size‐intensive transition moments from the coupled cluster singles and doubles linear response function
1994
Coupled cluster singles and doubles linear response (CCLR) calculations have been carried out for excitation energies and dipole transition strengths for the lowest excitations in LiH, CH+, and C4and the results compared with the results from a CI-like approach to equation of motion coupled cluster (EOMCC). The transition strengths are similar in the two approaches for single molecule calculations on small systems. However, the CCLR approach gives size-intensive dipole transition strengths, while title EOMCC formalism does not. Thus, EOMCC calculations can give unphysically dipole transition strengths, e.g., in EOMCC calculations on a sequence of noninteracting LiH systems we obtained a neg…
Random analysis of geometrically non-linear FE modelled structures under seismic actions
1990
Abstract In the framework of the finite element (FE) method, by using the “total Lagrangian approach”, the stochastic analysis of geometrically non-linear structures subjected to seismic inputs is performed. For this purpose the equations of motion are written with the non-linear contribution in an explicit representation, as pseudo-forces, and with the ground motion modelled as a filtered non-stationary white noise Gaussian process, using a Tajimi-Kanai-like filter. Then equations for the moments of the response are obtained by extending the classical Ito's rule to vectors of random processes. The equations of motion, and the equations for moments, obtained here, show a perfect formal simi…
Nonlinear dynamics of a two-photon Fabry–Pérot laser
2000
Abstract The steady-state emission, stability and temporal dynamics of a single-mode two-photon laser with a Fabry–Perot cavity is investigated and compared with that of a ring-cavity laser. It is found that the Fabry–Perot cavity makes the laser less efficient than the ring cavity because of spatial hole burning, but the domain of stability is larger for the Fabry–Perot laser. The intensity and phase dynamics are numerically investigated and distinctive features are found in the phase dynamics as compared with one-photon lasers.
Magic numbers, excitation levels, and other properties of small neutral 4He clusters (Nor = 50).
2006
The ground-state energies and the radial and pair distribution functions of neutral 4He clusters are systematically calculated by the diffusion Monte Carlo method in steps of one 4He atom from 3 to 50 atoms. In addition the chemical potential and the low-lying excitation levels of each cluster are determined with high precision. These calculations reveal that the "magic numbers" observed in experimental 4He cluster size distributions, measured for free jet gas expansions by nondestructive matter-wave diffraction, are not caused by enhanced stabilities. Instead they are explained in terms of an enhanced growth due to sharp peaks in the equilibrium concentrations in the early part of the expa…
Two-Photon Transitions in CW-ENDOR Spectra of Radicals in Fluid Solution
2002
The radical anion of duroquinone (2,3,5,6-tetramethyl-1,4-benzoquinone) was used as a model compound to describe the low-frequency (LF) ENDOR lines observed in many radical systems. These LF lines ...