Half-width temperature dependence of nitrogen broadened lines in the ν2 band of H2O

Forty-seven N₂ broadened water vapor line-widths have been measured in the 1845-2140 cm⁻¹ spectral range with a Fourier Transform spectrometer in the 258-330 K temperature range at a spectral resolution of 0.005 cm⁻¹ for the lines with upper state rotational quantum number up to 16. The measured exponents of the temperature dependence of the width exhibit a large range of values from 1.60 to −0.86. Theoretical calculations were made using a semi-empirical technique based on the Anderson theory. The calculated broadening coefficients as well as the temperature exponents for the half-width agree satisfactory with measured values.     

Optical limiters and diffraction elements based on a COANP-fullerene system: Nonlinear optical properties and quantum-chemical simulation

The results of optical study and quantum-chemical simulation of a conjugated organic system, 2-cyclooctylamino-5-nitropyridine (COANP)-fullerene, performed to determine its potential for application as a limiter of visible and near-IR laser radiation and as a material for diffraction elements in systems for reversible recording of optical information, are presented. Complexation between a COANP molecule and fullerene is considered as one of the main mechanisms responsible for the corresponding properties of this system. For the first time, nonlinear optical characteristics of COANP-C₆₀ and COANP-C₇₀ systems are comparatively studied and the intermolecular interaction between a COANP molecule and fullerene is analyzed on the quantum-chemical level.     

Symmetry of internal dynamics of the tetrahydrofuran molecule

A noninvariant geometrical group characterizing the internal dynamics of the tetrahydrofuran molecule C₄H₈O with allowance for the clearly pronounced pseudorotation effect is constructed. On this basis, some qualitative features of the energy spectrum of the molecule following from the analysis of high-resolution spectroscopic data are explained.     

Plasmon resonance in a nanosphere

The phenomenon of plasmon resonance in a nanosphere and a nanospheroid is considered. As is known, this phenomenon does not depend explicitly on the size of these nanoparticles. However, it is shown that, actually, the resonance conditions are determined by the diameter of the nanosphere and by the length of the major axis of the nanospheroid.     

Dependence of Doubly Charged Ion Formation by the Two-Electron Mechanism on the intensity of Laser Radiation

Experimental dependences of the doubly charged ion yield N ²⁺ on the laser radiation intensity F are analyzed for the case of ion formation by the two-electron mechanism. It is shown that the region where the dependence N ²⁺(F) is characterized by the degree of nonlinearity K≈2.5 corresponds to the saturation of the process of doubly charged ion formation. This region is described well by theoretical calculations performed for Gaussian laser beams.     

Effective Values of Variable Components of the Refractive Index upon Nonlinear Recording of Phase Holograms

The diffraction of a plane wave incident on a thick hologram at the first and second Bragg angles in the process of nonlinear recording is analyzed using the coupled-wave equations. It is shown that, in this case, the two-wave approximation with the use of effective modulation amplitudes of the refractive index, n _1ef and n _2ef, can be applied. Analytical dependences of n _1ef and n _2ef on the modulation amplitudes of the refractive index n ₁ and n ₂ at the fundamental and doubled spatial frequencies are obtained and the criteria of their applicability are determined. The dependences found are used to calculate the parameters of gratings recorded in a photopolymeric material.     

Absorption of electromagnetic radiation by an inhomogeneous spherical particle

The cross section of absorption of electromagnetic radiation by an inhomogeneous spherical particle is calculated. The general case of an arbitrary value of the ratio of the particle radius to the radius of the dielectric core is considered. The condition of diffuse reflection of electrons from the inner and outer surfaces of the metal layer of the particle is taken as the boundary condition of the problem. The limiting cases are considered and the results obtained are discussed.     

Computer processing of electronic absorption spectra of rare-earth elements in inorganic laser media

Algorithms and program modules are developed for calculation of the Judd-Ofelt parameters on modern computers. These programs can be used to perform numerical analysis of the energy absorption by rareearth ions in laser media.     

Polarized Fluorescence of Jet-Cooled indole and Carbazole and Their Complexes with Water

The spectra of the fluorescence excitation within the rotational contours of the bands of the pure electronic long-wavelength S ₀-S ₁ transitions of jet-cooled indole and carbazole molecules and their complexes with water are measured. For the carbazole-water complex, a contour with three maxima is registered, which is possibly related to the occurrence of two isomers, differing in a slight displacement of hydrogen between the nitrogen atom of the imine group of carbazole and the oxygen atom of the water molecule. The degrees of polarization of integral fluorescence upon excitation within the rotational contours of the S ₀-S ₁ electronic transition bands of the above molecules and their complexes with water are determined for the first time. The coincidence of the calculated (7.7%) and measured (7.3%) values of the degree of polarization upon excitation in the rotational Q branch of the ^b L ₁-A electronic transition of indole confirms the accepted intramolecular orientation of the transition dipole moment at an angle of 38.3° with respect to the principal axis of inertia A. Upon excitation of indole, its complex with water, and carbazole into the P and R branches, the measured and calculated degrees of polarization are also close to each other and amount to 2–3%. This confirms the occurrence of contributions to the fluorescence polarization due to the rotations of the indole molecules around the principal axes of inertia A and C.