Shell effects in the symmetric-modal fission of pre-actinide nuclei

Mass distributions of fragments in the low-energy fission of nuclei from ¹⁸⁷Ir to ²¹³At have been analysed. This analysis has shown that shell effects in symmetric-mode fragment mass yields from the fission of pre-actinide nuclei could be described if one assumes the existence of two strongly deformed neutron shells in the arising fragments with neutron numbers N₁ ≈ 52 and N₂ ≈ 68. A new method has been proposed for quantitatively describing the mass distributions of the symmetric fission mode for pre-actinides with A ≈ 180–220.     

Reaction dynamics of synthesis of superheavy elements

Based on the theory of the compound nucleus reaction, a brief review is given on the special aspects of the reaction dynamics in the synthesis of the superheavy elements (SHE), where the fusion probability is the most unknown factor. A new viewpoint of the fusion reaction is proposed that it consists of two processes; the first process up to the contact of two nuclei of the incident channel and the second one of a dynamical evolution to the spherical compound nucleus from the contact configuration. The fusion probability is, thus, given as a product of a contact probability and a formation probability. Analytic studies of the latter probability are discussed in the one-dimensional model, where a simple expression is given to the so-called extra-push energy in terms of the reduced friction, the curvature parameter of the conditional saddle point and the nuclear temperature. Preliminary results of numerical analyses of the contact probability are given, using the surface friction model (SFM). Remarks are given on the present status of our knowledge and for future developments. Received: 1 May 2001 / Accepted: 4 December 2001     

Cooling,identification and spectroscopy of super-heavy element ions

We briefly discuss some possibilities for cooling, identification and spectroscopy of super-heavy element (SHE) ions based on recent results obtained from studies of atomic and molecular ions in linear rf traps. Since these investigations only relied on the charge and the mass of the ion of interest, we believe it should be straight forward to adopt most of the techniques for SHE ion research.     

Hole and Electron Doping of the 4d Transition-Metal Oxyhydride LaSr3NiRuO4H4

Hole or electron doping of phases prepared by topochemical reactions (e.g. anion deintercalation or anion-exchange) is extremely challenging as these low-temperature conversion reactions are typically very sensitive to the electron counts of precursor phases. Herein we report the successful hole and electron doping of the transition-metal oxyhydride LaSr₃NiRuO₄H₄ by first preparing precursors in the range La_xSr_4−xNiRuO₈ 0.5<x<1.4 and then converting into the corresponding La_xSr_4−xNiRuO₄H₄ phases. This is particularly noteworthy as the (Ni/Ru)H₂ sheets in the La_xSr_4−xNiRuO₄H₄ phases are structurally analogous to the CuO₂ sheets in cuprate superconductors and hole doping (Ni^1+/2+, Ru²⁺) or electron doping (Ni²⁺, Ru^1+/2+) yields materials with partial occupancy in Ni/Ru –H 1s bands which are analogous to the partially occupied Cu –O 2p bands present in the CuO₂ sheets of doped superconducting cuprates.     

Charge-Tagged DNA Radicals in the Gas Phase Characterized by UV/Vis Photodissociation Action Spectroscopy

Adenosine radicals tagged with a fixed-charge group were generated in the gas phase and structurally characterized by tandem mass spectrometry, deuterium labeling, and UV/Vis action spectroscopy. Experimental results in combination with Born–Oppenheimer molecular dynamics, ab initio, and excited-state calculations led to unambiguous assignment of adenosine radicals as N-7 hydrogen atom adducts. The charge-tagged radicals were found to be electronically equivalent to natural DNA nucleoside radicals.     

Heavy-element chemistry --Status and perspectives

In the past ten years, nuclear chemists have made considerable progress in developing fast on-line separation techniques, which allowed to chemically characterize the first four transactinide elements Rf (rutherfordium, Z = 104), Db (dubnium, Z = 105), Sg (seaborgium, Z = 106), and recently also Bh (bohrium, Z = 107). In all cases the isolated nuclides were unambiguously identified by observing genetically linked decay chains. Nuclides with production cross-sections of less than 100 pb and half-lives as short as a few seconds have been chemically isolated. Thus, chemists have discovered or significantly contributed to the characterization of the nuclear-decay properties of a number of transactinide nuclei. New techniques with greatly improved overall efficiencies should allow chemists to extend their studies to even heavier elements such as Hs (hassium, Z = 108) and to the recently discovered superheavy elements with Z = 112 and 114, which can be produced only with picobarn cross-sections. Received: 21 March 2002 / Accepted: 16 May 2002 / Published online: 31 October 2002 RID="a" ID="a"e-mail: andreas.tuerler@psi.ch     

In-beam spectroscopy of 253, 254No

In-beam conversion electron spectroscopy experiments have been performed on the transfermium nuclei ^{253, 254}No using the conversion electron spectrometer SACRED in nearly collinear geometry in conjunction with the gas-filled separator RITU at the University of Jyv?skyl?. The experimental setup is discussed and the spectra are compared to Monte Carlo simulations. The implications for the ground-state configuration of ²⁵³No are discussed. Received: 21 March 2002 / Accepted: 16 May 2002 / Published online: 31 October 2002 RID="a" ID="a"e-mail: rdh@ns.ph.liv.ac.uk RID="b" ID="b"Present address: GANIL, F-14021 Caen, France. RID="c" ID="c"Permanent address: IReS Strasbourg, IN2P3-CNRS, F-67037-Strasbourg, France. RID="d" ID="d"Present address: CEA/DIF DCRE/SDE/LDN F-91680 Bruyeres-le-Chatel. RID="e" ID="e"Present address: Daresbury Laboratory, Daresbury WA4 4AD, UK. RID="f" ID="f"Permanent address: IPN Lyon, IN2P3-CNRS, F-69037 Lyon, France.     

Shell energy in the heaviest nuclei using the Green’s function oscillator expansion method

The Greens function oscillator expansion method and the generalized Strutinsky smoothing procedure are applied to shell corrections in the heaviest elements. A macroscopic-microscopic method with a finite deformed Woods-Saxon potential is used. The stability condition for the shell correction is discussed in detail and the parameters defining the smoothing procedure are carefully determined. It is demonstrated that the spurious contribution to the total binding energy due to the unphysical particle gas that appears in the standard method can be as large as 1.5 MeV for weakly bound neutron-rich superheavy nuclei, but the effect on energy differences (e.g., alpha-decay values) is fairly small.     

Structure of 231Ac: Measurements of level half-lives

There is lack of knowledge of the structure of the ²³¹Ac nucleus located in the upper border of the island of octupole deformation centered around A = 225. We have populated the excited states in ²³¹Ac by beta-decay from the parent ²³¹Ra produced at ISOLDE, CERN. The low-energy structure of ²³¹Ac has been investigated by means of γ, conversion electrons, γ-γ and γ-e^- spectroscopy. We report here in the precise determination in ²³¹Ac of the half-life of the most intensively populated states by the Advanced Time Delayed ββγ(t) technique.