Evidence for an isomeric 3/2- state in 53Co

The fragmentation of a 550MeV/u primary beam of ⁵⁸Ni on a ⁹Be target has been used to measure time- and energy-correlated γ decays following the implantation of event-by-event discriminated secondary fragments into a ⁹Be stopper plate. A new isomeric γ decay with T _1/2 = 14( ) ns and E _γ = 646.2(2) keV is observed and attributed to the decay of the yrast 3/2^- state in ⁵³ ₂₇Co₂₆ . This short-lived isomeric state has been populated by means of nuclear reactions during the stopping process of the secondary fragments. The experimental findings are discussed in the framework of large-scale spherical shell model calculations in conjunction with isospin symmetry-breaking residual interactions for the A = 53 , T _z = ±1/2 mirror nuclei ⁵³Co and ⁵³Fe .     

The electron affinity of tungsten

The electron affinity of tungsten has been measured using laser photodetachment threshold spectroscopy in a collinear geometry. The electron affinity was determined to 6583.6(6) cm^-1 by observing the onset of the process when W^- ions in the 5d⁵6s²5d^56s^2 ⁶S_5/2 ground state are photodetached producing neutral W atoms in the 5d⁴6s²5d^46s^2 ⁵D₀ ground state. The measured value is in agreement with previous measurements and improves the accuracy by almost two orders of magnitude. Further, a photodetachment signal below the ground state photodetachment threshold was found, which indicates the existence of a bound excited state in W^-.     

Resonances in Three-Body Systems Studied by a Full Angular-Momentum, Smooth-Exterior Complex-Scaling Finite-Element Method

 The development of a tool for calculating resonances and bound states in three-body systems described by a single-potential energy surface is reported. The method has been applied to the antiprotonic helium, doubly excited states in helium, the ¹¹Li nuclear halo, the NeICl van der Waals molecule, and the recently found FHD reaction complex. Received November 26, 2001; accepted for publication November 28, 2001     

Chiral hetero- and carbocyclic compounds from the asymmetric hydrogenation of cyclic alkenes

Several types of chiral hetero- and carbocyclic compounds have been synthesized by using the asymmetric hydrogenation of cyclic alkenes. N,P-Ligated iridium catalysts reduced six-membered cyclic alkenes with various substituents and heterofunctionality in good to excellent enantioselectivity, whereas the reduction of five-membered cyclic alkenes was generally less selective, giving modest enantiomeric excesses. The stereoselectivity of the hydrogenation depended more strongly on the substrate structure for the five- rather than the six-membered cyclic alkenes. The major enantiomer formed in the reduction of six-membered alkenes could be predicted from a selectivity model and isomeric alkenes had complementary enantioselectivity, giving opposite optical isomers upon hydrogenation. The utility of the reaction was demonstrated by using it as a key step in the preparation of chiral 1,3-cis-cyclohexane carboxylates.     

Linear Dichroism of Chloroplasts and Subchloroplast Fractions Oriented by Flow

Abstract

Chloroplasts as well as subchloroplast vesicles show linear dichroism (LD) when subjected to a hydrodynamic gradient. LD is positive for the ππ? in-plane polarized bands indicating that the chlorophyll porphyrin ring is in average oriented parallel1 to the elongated membrane surfaces. The vesicle fraction enriched inphotosystem I1 shows lower LD/A at 660 nm indicating lower average orientation of chlorophyll and the fraction enriched in photosystem I shows higher LD/A at 700 nm indicating that P700 is more oriented than the bulk chlorophyll.     

Electronic structure and chemical bonding of amorphous chromium carbide thin films

The microstructure, electronic structure and chemical bonding of chromium carbide thin films with different carbon contents have been investigated with high-resolution transmission electron microscopy, electron energy loss spectroscopy and soft x-ray absorption-emission spectroscopies. Most of the films can be described as amorphous nanocomposites with non-crystalline CrC(x) in an amorphous carbon matrix. At high carbon contents, graphene-like structures are formed in the amorphous carbon matrix. At 47 at.% carbon content, randomly oriented nanocrystallites are formed creating a complex microstructure of three components. The soft x-ray absorption-emission study shows additional peak structures exhibiting non-octahedral coordination and bonding.