First identification of excited states in the T_z\! = \!1/2 nucleus 93 Pd

The first experimental information about excited states in the N = Z + 1 nucleus ⁹³Pd is presented. The experiment was performed using a 205 MeV ⁵⁸Ni beam from the Vivitron accelerator at IReS, Strasbourg, impinging on a bismuth-backed ⁴⁰Ca target. Gamma-rays, neutrons and charged particles emitted in the reactions were detected using the Ge detector array Euroball, the Neutron Wall liquid-scintillator array and the Euclides Si charged-particle detector system. The experimental level scheme is compared with the results of new shell model calculations which predict a coupling scheme with aligned neutron-proton pairs to greatly influence the level structure of nuclei at low excitation energies.Received: 28 October 2003, Revised: 4 December 2003, Published online: 26 January 2004PACS: 21.10.Hw Spin, parity, and isobaric spin - 23.20.Lv transitions and level energies - 27.60. + j - 21.60.Cs Shell model     

Modern Michelson-Morley experiment using cryogenic optical resonators

We report on a new test of Lorentz invariance performed by comparing the resonance frequencies of two orthogonal cryogenic optical resonators subject to Earth's rotation over approximately 1 yr. For a possible anisotropy of the speed of light c, we obtain Delta(theta)c/c(0)=(2.6+/-1.7)x10(-15). Within the Robertson-Mansouri-Sexl (RMS) test theory, this implies an isotropy violation parameter beta-delta-1 / 2=(-2.2+/-1.5)x10(-9), about 3 times lower than the best previous result. Within the general extension of the standard model of particle physics, we extract limits on seven parameters at accuracies down to 10(-15), improving the best previous result by about 2 orders of magnitude.     

Precision test of the isotropy of light propagation

We report on a test of the isotropy of light propagation performed by comparing the resonance frequencies of two orthogonal cryogenic optical resonators subject to Earths rotation over 1yr. The technical aspects of the experiment are discussed and the analysis of the data is presented in detail. For a possible anisotropy of the speed of light c, we obtain c/c₀=(2.6±1.7)×10^-15. Within the general extension of the standard model of particle physics, we extract limits on seven parameters at accuracies down to 10^-15, improving the best previous result by about two orders of magnitude. Within the Robertson–Mansouri–Sexl test theory, this implies an isotropy-violation parameter --1/2=(2.2±1.5)×10^-9, about three times lower than the best previous result. PACS 03.30.+p; 12.60.-i; 06.30.Ft     

Kinetics of Hydrogenation and Variations in Resistance of Vanadium Thin Films Treated in Atomic Hydrogen Flow

Methods of nuclear reactions, x-ray diffraction analysis, transmission electron and nuclear microscopy were used to investigate the mechanism of hydrogenation of thin vanadium films in their treatment in a flow consisting of a mixture of molecular and atomic hydrogen. It has been shown that the main component penetrating into the metal from the gas phase is atomic hydrogen. At a gas pressure of 10^–2 Pa and room temperature, the dissolution of particles which, in the gas phase, are in molecular form, occurs at a much lower rate. It has been established that the (initially high) rate of variation of the hydrogen concentration in the film decreases during hydrogenation and gradually approaches zero. As this takes place, the hydrogen concentration in vanadium reaches its limiting value equal to about 42.5 at. %. A mathematical model of the hydrogenation of a vanadium film is proposed which describes experimental results based on the relaxation dependence of the hydrogen concentration on hydrogenation time. Comparative analysis of the variations in hydrogen concentration in a film and in film resistance is performed. It has been established that the dependence of the resistance on hydrogen concentration for a thin film hydrogenated in a flow of atomic hydrogen differs from the similar dependence for a bulk material hydrogenated in the atmosphere of molecular hydrogen under the conditions of thermodynamic equilibrium. The features of the behavior of the resistance of a thin film on hydrogenation time revealed experimentally are caused, as in the case of a bulk material, by the formation of the phase of vanadium hydride in the film. The possibility of using vanadium thin films for measuring absolute values of the atomic hydrogen flow density is discussed.     

Comparing simulation and experiment of a 2D granular Couette shear device

We present experiments along with molecular-dynamics (MD) simulations of a two-dimensional (2D) granular material in a Couette cell undergoing slow shearing. The grains are disks confined between an inner, rotating wheel and a fixed outer ring. The simulation results are compared to experimental studies and quantitative agreement is found. Tracking the positions and orientations of individual particles allows us to obtain density distributions, velocity and particle rotation rates for the system. The key issue of this paper is to show the extent to which quantitative agreement between an experiment and MD simulations is possible. Besides many differences in model details and the experiment, the qualitative features are nicely reproduced. We discuss the quantitative agreement/disagreement, give possible reasons, and outline further research perspectives.Received: 3 March 2003, Published online: 5 August 2003PACS: 45.70.-n Granular systems - 83.50.Ax Steady shear flows, viscometric flow - 83.10.Pp Particle dynamicsS. Luding: New address: Particle Technology, DelftChemTech, TU Delft, Julianalaan 136, 2628 BL Delft, The Netherlands;     

Coordination-driven self-assemblies with a carborane backbone

The design and self-assembly of five new supramolecular complexes (a rectangle, a triangle, a hexagon, and two squares) are described. These assemblies incorporate carborane building blocks and were prepared in excellent yields (>85%). The assemblies and building blocks were characterized with multinuclear NMR spectroscopy, electrospray ionization mass spectrometry, and elemental analysis. Isotopically resolved mass spectrometry data confirm the existence of the rectangle, triangle, and hexagon, and NMR data are consistent with the formation of all five assemblies. The X-ray structures of two linear carborane building blocks, 1,12-(4-CC(C(5)H(4)N)(2)-p-C(2)B(10)H(10) (1) and 1,12-(trans-(Pt(PEt(3))(2)I)CC)(2)-p-C(2)B(10)H(10) (2), are reported: 1 is monoclinic, P2(1)/c, a = 10.6791(4) A, b = 8.0091(14) A, c = 11.6796(4) A, beta = 107.8461(15) degrees , V = 950.89(5) A(3), Z = 2; 2 is monoclinic, C2/c, a = 62.1128(10) A, b = 22.0071(3) A, c = 14.0494(2) A, beta = 89.9411(8) degrees , V = 19204.4(5) A(3), Z = 16. Crystals of the linear linker 1 exhibit close pi-pi pyridine and pyridine-B(carborane) interactions, which are discussed.     

Shearing behavior of polydisperse media

We study the shearing of polydisperse and bidisperse media with a size ratio of 10. Simulations are performed with a two-dimensional shear cell using contact dynamics. With a truncated power law for the polydisperse media we find that they show a stronger dilatancy and greater resistance to shearing than bidisperse mixtures. To model additives used to control viscosity we introduce so-called “point-like particles”. Even changing the kinematic behavior very little, the point-like particles reduce the force necessary to maintain a fixed shearing velocity.     

New fluorescent probes reveal that flippase-mediated flip-flop of phosphatidylinositol across the endoplasmic reticulum membrane does not depend on the stereochemistry of the lipid

Glycerophospholipid flip-flop across biogenic membranes such as the endoplasmic reticulum (ER) is a fundamental feature of membrane biogenesis. Flip-flop requires the activity of specific membrane proteins called flippases. These proteins have yet to be identified in biogenic membranes and the molecular basis of their action is unknown. It is generally believed that flippase-facilitated glycerophospholipid flip-flop across the ER is governed by the stereochemistry of the glycerolipid, but this important issue has not been resolved. Here we investigate whether the ER flippase stereochemically recognizes the glycerophospholipids that it transports. To address this question we selected phosphatidylinositol (PI), a biologically important molecule with chiral centres in both its myo-inositol headgroup and its glycerol-lipid tail. The flip-flop of PI across the ER has not been previously reported. We synthesized fluorescence-labeled forms of all four diastereoisomers of PI and evaluated their flipping in rat liver ER vesicles, as well as in flippase-containing proteoliposomes reconstituted from a detergent extract of ER. Our results show that the flippase is able to translocate all four PI isomers and that both glycerol isomers of PI flip-flop across the ER membrane at rates similar to that measured for fluorescence-labeled phosphatidylcholine. Our data have important implications for recent hypotheses concerning the evolution of distinct homochiral glycerophospholipid membranes during the speciation of archaea and bacteria/eukarya from a common cellular ancestor.     

Phase relations, quasicontinuous spectra and subfemtosecond pulses in high-order stimulated raman scattering with short-pulse excitation

High-order stimulated Raman scattering for pumping by ps and sub-ps pulses is studied in the frame of a time-domain approach without the slowly varying envelope approximation. Formation of pulse trains with sub-fs durations in the ps-pump regime is demonstrated using external phase compensation. For sub-ps excitation a novel broadening mechanism of Raman lines is predicted that leads to a quasicontinuous spectrum and permits one to generate single sub-fs pulses. We predict also essential shortening of a delayed fs-probe pulse by the Raman oscillations without phase control.