Descripción: Fil:Depine, R.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.

Descripción: We present radio observations of the source G332.5-5.6, a candidate supernova remnant (SNR). Observations have been performed with the Australia Telescope Compact Array (ATCA) at two frequencies, 1.4 and 2.4 GHz. Our results confirm that G332.5-5.6 is an SNR, with a spectral index α = -0.7 ± 0.2 for the whole source and an average fractional polarization of ∼35 per cent at 2.4 GHz. The central component is coincident with extended X-ray emission, and the distance to the SNR is estimated to be ∼3.4 kpc. Based on its radio and X-ray morphology, this SNR should be classified as a composite, and we suggest that it belongs to a trident-shaped subclass like G291.0-0.1. © 2006 RAS.

Descripción: We present results on the quark and gluon polarization in the nucleon obtained in a combined next to leading order analysis to the available inclusive and semi-inclusive polarized deep inelastic scattering data. © 2005 American Institute of Physics.

Descripción: We present CDW-EIS theoretical calculations for the projectile deflection in single ionization of Helium by heavy-ion impact as a function of ionized electron energies. These calculations account for the projectile-residual target ion interaction through a first order static potential and a second order polarization potential. The results are compared with recent experimental data by impact of 3.6 MeV/amu Au53+. A good agreement is found. © 2007 IOP Publishing Ltd.

Descripción: We investigate the potential impact of forthcoming Jefferson Lab semi-inclusive polarized deep inelastic scattering proton measurements in the determination of the sea quark polarization in the nucleons by means of a next to leading order global QCD analysis. Specifically, we estimate the resulting improvement in the constraints on polarized parton densities for different flavors, which is found to be significant for up and strange quarks, and the correlation between remaining uncertainty ranges for each of the parton species.

Descripción: The purpose of this review is to examine and discuss the ways in which water is organized at the interface of a biological membrane. The relevance of this structure to the surface properties and to the adsorption of proteins in membranes is also analized. The approach is based on the idea that cell functions are confined to a restricted water media, the cell interior, in which the proximity of the membrane may be key to regulating the enzyme activity and the cell membrane permeability. As the lipid bilayer is the structural base of cell membranes, the distribution of water in the surface sites of a phospholipid membrane is analyzed by means of Fourier Transform spectrometry. The polarization of water at the surface was looked into through the measure of surface potentials and the dynamics of the surface hydration by cyclic voltammetry. Modification of these properties by the replacement of water by polyol molecules such as trehalose and phloretin and by the insertion of aqueous soluble enzymes, has also been investigated.

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: In this work we investigate experimentally and theoretically angular distributions of swift multi-electronic atoms after colliding with a LiF(001) surface under axial surface channeling conditions. We use the surface eikonal approximation to describe the quantum interference of scattered projectiles. The atom-surface interaction is represented by means of a pairwise additive potential that includes the contribution of the projectile polarization. The aim is to use the experimental spectra to test the range of validity of the proposed potential model. © Published under licence by IOP Publishing Ltd.

Descripción: High resolution spectra in polarized light of oriented crystalline films of chloroform at 77°K were obtained. The ratio of intensities of Davydov components for different angles of polarization were also determined. Comparison with the oriented gas model approximation allowed the assignment of components to the proper representations of the D 2h factor group : all bands were assigned to the infrared active factor group symmetry species B 1u, B 2u, and B 3u corresponding to vibrations along a, b, and c crystallographic axes. Comparison with results of measurements in solid solutions in argon made by King allowed the distinction between crystallographic effect and isotopic shifts.

Descripción: The resolution of molecular electric dipole polarizabilities into atomic contributions was studied in the context of methyl and ethyl derivatives, CH3-X and CH3-CH2-X. The reliability of the partitioning schemes allowing for adhoc quantum chemical tools was also tested. Results depicted a good degree of the transferability from molecule to molecule as shown by the evaluation of gross atomic isotropic contributions for carbon, hydrogen, and heteroatoms.

Descripción: The conventional random phase approximation (RPA) of the polarization propagator theory and a computational method based on continuous transformation of origin for the current density (CTOCD) induced within the electron cloud by an external homogeneous, static magnetic field has been employed to calculate atomic contributions to magnetic susceptibilities. The diamagnetic part of the magnetic susceptibility is written in terms of the polarization propagator. Since the paramagnetic term may also be obtained from the propagator it is thus possible to compute both contributions at the same level of approximation. The evaluated average susceptibility is independent of the origin of the vector potential, but depends on the origin of the reference frame. The atomic contributions to the diamagnetic and paramagnetic parts of the magnetic susceptibility are derived by applying off-diagonal hypervirial relations which are exactly fulfilled if the state functions are exact eigenfunctions of a model Hamiltonian. The rationalization of the magnetic susceptibilities into atomic contributions is applied to some small molecules: HF, H2O, NH3 and CH4, and the sum of these contributions is compared to the corresponding calculated total values and the experimental data for the molecular magnetic susceptibility for the same compounds. Computations are performed using basis sets of increasing quality. A series of sum rules for gauge independence of the computed results and charge-current conservation have been tested to document the accuracy of the calculation of magnetic properties. © 1999 American Institute of Physics.

Descripción: Ring polymer molecular dynamics experiments have been carried out to examine effects derived from nuclear quantum fluctuations at ambient conditions on equilibrium and non-equilibrium dynamical characteristics of charge solvation by a popular simple, rigid, water model, SPC/E, and for a more recent, and flexible, q-TIP4P/F model, to examine the generality of conclusions. In particular, we have recorded the relaxation of the solvent energy gap following instantaneous, ±e charge jumps in an initially uncharged Lennard-Jones-like solute. In both charge cases, quantum effects are reflected in sharper decays at the initial stages of the relaxation, which produce up to a ∼20% reduction in the characteristic timescales describing the solvation processes. For anionic solvation, the magnitude of polarization fluctuations controlling the extent of the water proton localization in the first solvation shell is somewhat more marked than for cations, bringing the quantum solvation process closer to the classical case. Effects on the solvation response from the explicit incorporation of flexibility in the water Hamiltonian are also examined. Predictions from linear response theories for the overall relaxation profile and for the corresponding characteristic timescales are reasonably accurate for the solvation of cations, whereas we find that they are much less satisfactory for the anionic case. © 2013 AIP Publishing LLC.

Descripción: We use ring-polymer-molecular-dynamics (RPMD) techniques and the semi-empirical q-TIP4P/F water model to investigate the relationship between hydrogen bond connectivity and the characteristics of nuclear position fluctuations, including explicit incorporation of quantum effects, for the energetically low lying isomers of the prototype cluster [H2O] 8 at T = 50 K and at 150 K. Our results reveal that tunneling and zero-point energy effects lead to sensible increments in the magnitudes of the fluctuations of intra and intermolecular distances. The degree of proton spatial delocalization is found to map logically with the hydrogen-bond connectivity pattern of the cluster. Dangling hydrogen bonds exhibit the largest extent of spatial delocalization and participate in shorter intramolecular O-H bonds. Combined effects from quantum and polarization fluctuations on the resulting individual dipole moments are also examined. From the dynamical side, we analyze the characteristics of the infrared absorption spectrum. The incorporation of nuclear quantum fluctuations promotes red shifts and sensible broadening relative to the classical profile, bringing the simulation results in much more satisfactory agreement with direct experimental information in the mid and high frequency range of the stretching band. While RPMD predictions overestimate the peak position of the low frequency shoulder, the overall agreement with that reported using an accurate, parameterized, many-body potential is reasonable, and far superior to that one obtains by implementing a partially adiabatic centroid molecular dynamics approach. Quantum effects on the collective dynamics, as reported by instantaneous normal modes, are also discussed. © 2013 AIP Publishing LLC.

Descripción: In previous works, we presented 2-D and 3-D magnetotelluric modelling methods based on Rayleigh-Fourier expansions. These methods are an alternative to finite-element and finite-difference techniques and are especially suitable for modelling multilayered structures, with smooth irregular boundaries. Here we generalize the 2-D method for the calculation of the electromagnetic response of 2-D structures to arbitrary, spatially non-uniform 2-D and 3-D inducing magnetic fields. These fields are characteristic of low- and high-latitude regions. We calculate the response to different 2-D and 3-D sources, of a 2-D structure representative of the conductivity distribution which could be found at a coastline, which includes deep conductive anomalies in the lower crust and upper mantle. Then, we investigate source effects, comparing these responses to that obtained for a uniform source. These effects become noticeable for periods greater than approximately 6 h and increase with the period of the source. They are highly dependent on the morphology of the source and also on the orientation of the external field relative to the strike direction of the structure. In various cases, they totally mask the uniform source response.

Descripción: We assessed the intracellular association states of the Parkinson's disease related protein α-synuclein (AS) in living cells by transfection with a functional recombinant mutant protein (AS-C4) bearing a tetracysteine tag binding the fluorogenic biarsenical ligands FlAsH and ReAsH, The aggregation states of AS-C4 were assessed by in situ microscopy of molecular translational mobility with FRAP (fluorescence recovery after photobleaching) and of local molecular density with confocal fluorescence anisotropy (CFA). FRAP recovery was quantitative and rapid in regions of free protein, whereas AS in larger aggregates was>80% immobile. A small 16% recovery characterized by an apparent diffusion constant of 0.03-0.04 μm 2/s was attributed to the dynamics of smaller, associated forms of AS-C4 and the exchange of mobile species with the larger immobile aggregates. By CFA, the larger aggregates exhibited high brightness and very low anisotropy, consistent with homoFRET between closely packed AS, for which a Förster distance (R o) of 5.3 nm was calculated. Other bright regions had high anisotropy values, close to that of monomeric AS, and indicative of membrane-associated protein with both low mobility and low degree of association. The anisotropy-fluorescence intensity correlations also revealed regions of free protein or of small aggregates, undetectable by conventional fluorescence imaging alone. The combined strategy (FRAP+CFA) provides a highly sensitive means for elucidating both the dynamics and structural features of protein aggregates and other intracellular complexes in living cells, and can be extended to other amyloid systems and to drug screening protocols. © 2011 Roberti et al.

Descripción: Computational procedures, based on (i) the Ramsey common origin approach and (ii) the continuous transformation of the origin of the quantum mechanical current density-diamagnetic zero (CTOCD-DZ), were applied at the Hartree-Fock level to determine electric quadrupole polarizabilities of nuclear magnetic shielding for molecules in the presence of a nonuniform electric field with a uniform gradient. The quadrupole polarizabilities depend on the origin of the coordinate system, but values of the magnetic field induced at a reference nucleus, determined via the CTOCD-DZ approach, are origin independent for any calculations relying on the algebraic approximation, irrespective of size and quality of the (gaugeless) basis set employed. On the other hand, theoretical estimates of the induced magnetic field obtained by single-origin methods are translationally invariant only in the limit of complete basis sets. Calculations of electric quadrupole polarizabilities of nuclear magnetic shielding are reported for H2, HF, H2 O, N H3, and C H4 molecules. © 2008 American Institute of Physics.

Descripción: We extend our previous molecular dynamics experiments [Rodriguez, J. Phys. Chem. B 109, 24427 (2005)] to the analysis of the adsorption of catanionic surfactants at water/air interfaces, at a surfactant coverage close to that of the saturated monolayer: 30.3 Å2 per headgroup. The mixture of surfactants investigated corresponds to equal amounts of dodecytrimethylammonium (DTA) and dodecylsulfate (DS). The structure of the interface is analyzed in terms of the local densities and orientational correlations of all relevant interfacial species. In accordance with experimental evidence, the DTA headgroups penetrate deeper into the aqueous substrate than the DS ones, although the average positions of all headgroups, with respect to the interface, lie in positions somewhat more external than the ones observed at lower coverages. Average tail tilts are close to 45°. The characteristics of the headgroup-water substrate correlations are also analyzed using a tessellation procedure of the interface. The density and polarization responses of the interfacial domains closest to the DS headgroups are enhanced, compared to those adjacent to the DTA detergents. Dynamical aspects related to the diffusion and to the orientational correlations of different water layers in close contact with the surfactant are also investigated. © 2007 American Institute of Physics.

Descripción: Herein we present a detailed analysis of the optical response of artificial opal films realized employing a near-field scanning optical microscope in collection and transmission modes. Near-field patterns measured at the rear surface when a plane wave impinges on the front face are presented with the finding that optical intensity maps present a clear correlation with the periodic arrangement of the outer surface. Calculations based on the vector Korringa-Kohn-Rostoker method reproduce the different profiles experimentally observed as well as the response to the polarization of the incident field. These observations constitute the first experimental confirmation of the collective lattice resonances that give rise to the optical response of these three dimensional periodic structures in the high-energy range. © 2011 American Institute of Physics.

Descripción: Imaging of samples by different microscopy techniques has produced a relevant impact in the development of new diagnosis techniques in biology, medicine and material science. In many biological, applications, where the sample changes or moves during the observation, a moving spot to track an identified sample is required. We introduce here an optical system that can perform, this tracking without mechanical components. The system, is based on the use of a high resolution liquid crystal on silicon (LCoS) device working as a mostly phase wave front modulator. The additional advantage of this system is performing the motion of the spot at video rate. In general, these devices produce coupled phase and amplitude modulation responses as a function of the applied voltage. This coupling effect deteriorates the response of those ideal optical elements designed as phase only or amplitude only functions. By means of an elliptical polarization light we can reduce the amplitude modulation and improve the phase modulation. We have experimentally found a configuration where the amplitude is almost constant while the phase reaches a high modulation. For this configuration we show how the spot can be moved through, focus plane by means of linear phases, or displaced out of this plane by using a quadratic phase. © 2008 American Institute of Physics.