Neutron halo isomers in stable nuclei and their possible application for the production of low energy, pulsed, polarized neutron beams of high intensity and high brilliance

We propose to search for neutron halo isomers populated via γ-capture in stable nuclei with mass numbers of about A=140–180 or A=40–60, where the 4s _1/2 or 3s _1/2 neutron shell model state reaches zero binding energy. These halo nuclei can be produced for the first time with new γ-beams of high intensity and small band width (≤0.1%) achievable via Compton back-scattering off brilliant electron beams, thus offering a promising perspective to selectively populate these isomers with small separation energies of 1 eV to a few keV. Similar to single-neutron halo states for very light, extremely neutron-rich, radioactive nuclei (Hansen et al. in Annu. Rev. Nucl. Part. Sci. 45:591–634, 1995; Tanihata in J. Phys. G., Nucl. Part. Phys. 22:158–198, 1996; Aumann et al. in Phys. Rev. Lett. 84:35, 2000), the low neutron separation energy and short-range nuclear force allow the neutron to tunnel far out into free space much beyond the nuclear core radius. This results in prolonged half-lives of the isomers for the γ-decay back to the ground state in the 100 ps-μs range. Similar to the treatment of photodisintegration of the deuteron, the neutron release from the neutron halo isomer via a second, low-energy, intense photon beam has a known much larger cross section with a typical energy threshold behavior. In the second step, the neutrons can be released as a low-energy, pulsed, polarized neutron beam of high intensity and high brilliance, possibly being much superior to presently existing beams from reactors or spallation neutron sources.     

Synthesis of primary amines: first homogeneously catalyzed reductive amination with ammonia

[reaction: see text] The synthesis of primary amines via reductive amination of the corresponding carbonyl compounds with aqueous ammonia is achieved for the first time with soluble transition metal complexes. Up to an 86% yield and a 97% selectivity for benzylamines were obtained in the case of various benzaldehydes by using a Rh-catalyst together with water-soluble phosphine and ammonium acetate. In the case of aliphatic aldehydes, a bimetallic catalyst based on Rh/Ir gave improved results.     

Poly(3-hydroxybutyrate)-depolymerase from Pseudomonas lemoignei: catalysis of esterifications in organic media

Lipase catalysis in nonaqueous media is recognized as a powerful tool in organic and more recently polymer synthesis. Even though none of the currently known polyhydroxyalkanoate (PHA) depolymerases have lipase activity, they do have a catalytic center that resembles that of lipases. Motivated by the above, the potential of using the poly(3-hydroxybutyrate), PHB, depolymerase from Psuedomonas lemoignei in organic media to catalyze ester-forming reactions was investigated. The effect of different organic solvents (benzene-d(6), cyclohexane-d(12), and acetonitrile-d(3)) on the activity of the PHB-depolymerase toward propylation of L-lactide was studied. A significant difference in the catalytic rate was observed as a function of solvent polarity. The selectivity of the PHB-depolymerase (P. lemoignei) to catalyze the propylation of a series of different lactones including epsilon-caprolactone, delta-butyrolactone, gamma-butyrolactone, and D, L, meso, and racemic lactides has been studied with the PHB-depolymerase (P. lemoignei) in organic solvents. Important differences in the reactivity of these lactones, as well as selective hydrolysis of stereochemically different linear lactic acid dimers, were observed. Moreover, the ability of the PHB-depolymerase to catalyze the solventless polymerization of epsilon-caprolactone and trimethylene carbonate was investigated.     

Location of alkali metal binding sites in endothelin A selective receptor antagonists, cyclo(D-Trp-D-Asp-Pro-D-Val-Leu) and cyclo(D-Trp-D-Asp-Pro-D-Ile-Leu), from multistep collisionally activated decompositions

We previously showed by using mass spectrometry that endothelin A selective receptor antagonists BQ123 and JKC301 form novel coordination compounds with sodium ions. This property may underlie the ability of an ET(A) antagonist to induce net tubular sodium reabsorption in the proximal tubule cells and reverse acute renal failure induced by severe ischemia. We have now defined the metal binding sites on BQ123 and JKC301 by subjecting the metal-containing peptides to multiple stages of collisionally activated decomposition (CAD) in an ion trap mass spectrometer. When submitted to low-energy CAD, the ring opens at the Asp-Pro amide bond. The metal ion, which bonds, inter alia, to the carbonyl oxygen of the proline residue, acts as a fixed charge site, and directs a charge-remote, sequence-specific fragmentation of the ring-opened peptide. Amino acid residues are sequentially cleaved from the C-terminal end, and the terminal aziridinone structure moves one step toward the N-terminus with each C-terminal amino acid residue removed. These observations are the basis of a new method to sequence cyclic peptides. Amino acid residues are observed as sets of three ions, a*(n)PD, b*(n)PD and c*(n)PD where n is the number of amino acid residues in the peptide.     

JASMS starts its tenth year

Editorial

JASMS starts its tenth year     

Promises, hopes, and hyperbole: adoption of new informationtechnologies

Much of the talk about the information revolution so far is just that-talk. A provocative mix of promises, hopes and hyperbole, some of it will come true over time. Most of it will not. Technology is moving at ever-increasing speeds, and predictions about technology are accelerating even faster. Yet practical needs and wants rarely keep pace. The purpose of this paper is to explore the disparity between the promises and possibilities of the information revolution. It examines the factors that traditionally affect new technologies, and the role of end-users in affecting outcomes     

Quantitative infrarotspektroskopische Analyse von Styrol-Acrylnitril-Copolymeren nach pyrolytischer Zersetzung

Ohne Zusammenfassung

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Quantitative infrared-speotroscopic analysis of styrene-acrylonitrile copolymers after pyrolytic decomposition

     

Charge transfer prior to fusion

Zeitschrift für Physik A Hadrons and nuclei - In reactions between very asymmetric projectile-target systems charge is preferably transferred from the lighter to the heavier nucleus. This...