Descripción: A general method is presented for computing matrix elements of quark operators on baryonic states with low strangeness and arbitrary number of colors N c . These results are useful in applications of the large N c expansion to baryons and exotics. As an application we compute the matrix elements of strangeness changing operators contributing to kaon couplings to ground state baryons and pentaquarks, in broken SU (3). © 2006 Elsevier B.V. All rights reserved.

Descripción: Solvation of excess electrons in supercritical ammonia along the T = 450 K isotherm was investigated. Equilibrium aspects of solvation were analyzed using combined path integral-molecular dynamics techniques. Observations showed transition from localized to quasifree states at approximately one fourth of the triple point density.

Descripción: The fluorescence emission of merocyanine 540 (MC540) in 95% ethanol was studied under continuous irradiation. Fluorescence spectra from excited states of both normal (N) and photoisomeric (P) species are identical. The laser fluence dependence of the fluorescence intensity is interpreted on the basis of a photochromic system involving N and P ground states and first excited singlet states. Common flash photolysis equations are generalized in order to include a photoequilibrium between isomers. The emission data are used together with previous flash photolysis and optoacoustic results to obtain P fluorescence and photoisomerization quantum yields as 0.07 ± 0.02 and 0.20 ± 0.04, respectively, P absorption cross section at the maximum (560 nm) as 4.74 × 10-16 cm2 (125 × 103 M-1·cm-1), and the energy difference between the ground states as 165 kJ·mol-1. Internal conversion, which can take place as a direct process or through a twisted state, is the main deactivation pathway for excited singlet P. © 1990 American Chemical Society.

Descripción: Our previously developed analytical infinite order sudden quantum theory of triatomic photodissociation is generalized to compute fragment internal energy distributions when the initial triatomic rotational state has K ≠ 0. The dependence of product rotational energy distributions on initial rotational and vibrational state is illustrated through model computations for the direct NOCl photodissociation from the ground to the T1(1 3A″) potential energy surface. The calculations consider all J,K ≤ 9 and employ a repulsive potential that is fit to ab initio computations. Comparisons of fragment rotational distributions with previous semiclassical approximations further elucidate the role of the mapping of the initial state bending wave function onto the fragment rotational distributions and the influence of parent rotations on this mapping. The infinite order sudden quantum-mechanical distributions exhibit a more complex structure, but upon thermal averaging they are already transformed at T = 3 K into fairly broad rotational distributions. The present theory readily permits the calculations of energy distributions for initial states of high J and K. © 1994 American Institute of Physics.

Descripción: New insights into equilibrium and dynamical aspects of electron photodetachment reactions in small water clusters were given. It focuses on assessing the effects of thermal and polarization fluctuations provided by three cluster environments with different extents of spatial confinement, on the microscopic mechanisms that drive the reaction. These fluctuations, in turn, determine the characteristics of the electron localization and the subsequent detachment following photoexcitation of the probe.

Descripción: A two-component theory for shielding calculations starting from a four-component Rayleigh-Schrodinger perturbation theory (RSPT) formalism is presented. Thus, a set of operators entering the RSPT expressions in terms of the Schrodinger molecular spectrum are derived by expanding such four-component expression as a power series in c-1. All formal expressions are retained, without neglecting any terms in the intermediate steps of the derivation.

Descripción: An approach was developed to determine triplet quantum yields, ΦT, which overcomes most of the difficulties usually encountered in flash photolysis studies of triplet states. The combined application of near-IR emission and optoacoustics yields ΦT values which are independent of the absorption properties of the triplets. Thus, the triplet energies derived from near-IR phosphorescence spectra together with the values of the heat stored by the triplets determined from optoacoustic experiments afforded ΦT = 0.3 ± 0.1 for porphycene (PO) and 0.4 ± 0.1 for its tetra-n-propyl derivative (TPrPO). Several calorimetric references for optoacoustic measurements in the red region were tested. The ΦT values, combined with flash photolysis data, yielded accurate triplet- minus ground-state absorption coefficients. The quantum yields for singlet molecular oxygen production determined by time-resolved phosphorescence were ΦΔ = 0.34 ± 0.05 for PO and 0.36 ± 0.03 for TPrPO which implies an efficiency near unity for O2(1Δ8) production upon collision of the triplet states of the porphycenes with ground-state O2. © 1990 American Chemical Society.

Descripción: Vertical excitation and electron detachment energies associated with the optical absorption of iodide ions dissolved in supercritical ammonia at 420 K have been calculated in two limiting scenarios: as a solvated free I- ion and forming a K+ I- contact ion pair (CIP). The evolution of the transition energies as a result of the gradual building up of the solvation structure was studied for each absorbing species as the solvent's density increased, i.e., changing the N H3 supercritical thermodynamic state. In both cases, if the solvent density is sufficiently high, photon absorption produces a spatially extended electron charge beyond the volume occupied by the solvated solute core; this excited state resembles a typical charge-transfer-to-solvent (CTTS) state. A combination of classical molecular dynamics simulations followed by quantum mechanical calculations for the ground, first-excited, and electron-detached electronic states have been carried out for the system consisting of one donor species (free I- ion or K+ I- CIP) surrounded by ammonia molecules. Vertical excitation and electron detachment energies were obtained by averaging 100 randomly chosen microconfigurations along the molecular dynamics trajectory computed for each thermodynamic condition (fluid density). Short- and long-range contributions of the solvent-donor interaction upon the CTTS states of I- and K+ I- were identified by performing additional electronic structure calculations where only the solvent interaction due to the first neighbor molecules was taken into account. These computations, together with previous experimental evidence that we collected for the system, have been used to analyze the solvent effects on the CTTS transition. In this paper we have established the following: (i) the CTTS electron of free I- ion or K+ I- CIP presents similar features, and it gradually localizes in close proximity of the iodine parent atom when the ammonia density is increased; (ii) for the free I- ion, the short-range solvent interaction contributes to the stabilization of the ground state more than it does for the CTTS excited state, which is evidenced experimentally as a blueshift in the maximum absorption of the CTTS transition when the density is increased; (iii) this effect is less noticeable for the K+ I- ion pair, because in this case a tight solvation structure, formed by four N H3 molecules wedged between the ions, appears at very low density and is very little affected by changes in the density; (iv) the long-range contribution to the solvent stabilization can be neglected for the K+ I- CIP, since the main features of its electronic transition can be explained on the basis of the vicinity of the cation; (v) however, the long-range solvent field contribution is essential for the free I- ion to become an efficient CTTS donor upon photoexcitation, and this establishes a difference in the CTTS behavior of I- in bulk and in clusters. © 2007 American Institute of Physics.

Descripción: A programme is outlined for the assembly of a comprehensive dielectronic recombination database within the generalized collisional-radiative (GCR) framework. It is valid for modelling ions of elements in dynamic finite-density plasmas such as occur in transient astrophysical plasmas such as solar flares and in the divertors and high transport regions of magnetic fusion devices. The resolution and precision of the data are tuned to spectral analysis and so are sufficient for prediction of the dielectronic recombination contributions to individual spectral line emissivities. The fundamental data are structured according to the format prescriptions of the Atomic Data and Analysis Structure (ADAS) and the production of relevant GCR derived data for application is described and implemented following ADAS. The requirements on the dielectronic recombination database are reviewed and the new data are placed in context and evaluated with respect to older and more approximate treatments. Illustrative results validate the new high-resolution zero-density dielectronic recombination data in comparison with measurements made in heavy-ion storage rings utilizing an electron cooler. We also exemplify the role of the dielectronic data on GCR coefficient behaviour for some representative light and medium weight elements.

Descripción: A novel method for simulating the statistical mechanics of molecular systems in which both nuclear and electronic degrees of freedom are treated quantum mechanically is presented. The scheme combines a path integral description of the nuclear variables with a first-principles adiabatic description of the electronic structure. The electronic problem is solved for the ground state within a density functional approach, with the electronic orbitals expanded in a localized (Gaussian) basis set. The discretized path integral is computed by a METROPOLIS Monte Carlo sampling technique on the normal modes of the isomorphic ring polymer. An effective short-time action correct to order τ4 is used. The validity and performance of the method are tested by studying two small lithium clusters, namely Li4 and Li5+. Structural and electronic properties computed within this fully quantum-mechanical scheme are presented and compared to those obtained within the classical nuclei approximation. Quantum delocalization effects turn out to be significant as shown by the fact that quantum simulation results at 50 K approximately correspond to those of classical simulations carried out at 150 K. The scaling factor depends, however, on the specific physical property, thus evidencing the different character of quantum and thermal correlations. Tunneling turns out to be irrelevant in the temperature range investigated (50-200 K). © 1998 American Institute of Physics.

Descripción: The confinement of Ar in planar slits of two identical parallel semi-infinite walls of alkali metals, alkaline-earth metal Mg, and CO 2 is investigated within the framework of the density functional theory. It is assumed that (1) the fluid atoms interact via a recently proposed effective attractive pair potential with strength, εff, which reproduces the experimental data of the surface tension of the liquid-vapor interface at the bulk coexistence curve, and (2) the adsorption on the walls is described by ab initio potentials characterized by a well depth, Wsf. In this way the systems were studied in the framework of a realistic approach. We found that for small coverages, the slit is always filled by forming two symmetric vapor films, one at each wall. For increasing coverage the behavior depends on the ratio Wsf/εff and the temperature T. In the case of alkali metals, we found at the triple point, Tt, of the adsorbate a regime of average density ρ*av in which the ground state exhibits asymmetric density profiles, leading to the so-called spontaneous symmetry breaking (SSB) effect. The SSB appears at an average density ρ*sb1 and disappears at a higher average density ρ*sb2 . When T is increased, the range of densities ρ*sb1≤ρ*av≤ ρ* sb2 diminishes and eventually the SSB disappears at a critical temperature, Tsb, which coincides with the critical prewetting temperature Tcpw observed in the adsorption on a single wall. For T>Tcpw the slit is filled symmetrically up to the phase transition to capillary condensation. All these features are examined as a function of the strength of the substrate and the width of the slit. Furthermore, no SSB effect was found for Mg and CO2. © 2010 American Institute of Physics.