Generalized seniority in the presence of strong shell effects

Generalized seniority is shown to provide a useful variational formalism for alike-nucleon systems even in the presence of strong shell effects.     

New coupling scheme in the interacting boson-fermion model: O(6) spectra in odd-A nuclei

We suggest that a new coupling scheme, based on the O(6) boson symmetry, may be useful in describing the spectra of odd-A nuclei towards the end of major shells. We describe the main properties of this scheme and show one example of it.     

Multilevel description of the Rh isotopes in the interacting boson-fermion model

We present a multilevel calculation within the framework of the interacting boson-fermion model (IBFM-1) of the odd-mass ^101–109Rh isotopes. We calculate both positive- and negative-parity states of the same hamiltonian, starting from the $\text{1g}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}$, $\text{2p}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$, $\text{2p}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$, $\text{lf}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ and $\text{2d}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ single-particle orbitals. We discuss energy spectra, electromagnetic E2 transition rates and one-nucleon transfer properties. We also discuss the influence of the $\text{1f}{}_{\mathrm{<mtext>7</mtext><mtext>2</mtext>}}$ orbital on the one-nucleon transfer properties. The results of the calculation for the negative-parity states are compared with the results of the $\text{U(}\text{6}\text{12}$) supersymmetry scheme of the interacting boson model.     

The proton complex of a diaza-macropentacycle: structure, slow formation, and chirality induction by ion pairing with the optically active 1,1'-binaphthyl-2,2'-diyl phosphate anion

The protonation of a sterically crowded [N2S6] macropentacycle (1) with 1 equiv of CF3SO3H in CDCl3 is slow and gives the singly (oo(+) [1 x H](+)) and doubly (o(+)o(+) [1 x 2H](2+)) protonated forms as kinetic products, the i(+)o form of [1 x H](+) being the thermodynamic product. i(+)o [1 x H](+) is C3 helically chiral in the solid state and in solution. The barrier to racemization (DeltaG(double dagger)) of the [1 x H](+) propeller is >71 kJ mol(-1). The ammonium proton is encapsulated in the tetrahedral coordination sphere provided by the endo (i) nitrogen bridgehead atom and the three proximal thioether sulfurs, which makes [1 x H](+) a proton complex. Use of the optically active acid (R)-(-)- or (S)-(+)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate (BNPH) in chloroform allowed us to induce a significant diastereomeric excess (24% de), which produced a detectable ICD. The de was decreased in acetone-d6 (10%), suggesting that the sense of chirality of [1 x H](+) is controlled by ion-pair interactions. Detailed NMR studies allowed us to locate the chiral anion on the endo side of [1 x H](+), in the cavity lined by endo t-Bu groups, and to establish that the rate of anion exchange in [1 x H][(S,R)-(+/-)-BNP] was higher than the rate of propeller inversion of [1 x H](+).     

Looking at self-consistent-charge density functional tight binding from a semiempirical perspective

The self-consistent-charge density functional tight binding (SCC-DFTB) method is compared with other semiempirical methods (MNDO, AM1, PM3, OM1, OM2, OM3). Despite the differences in the underlying philosophy and derivation, these methods share many common features. Systematic evaluations of their performance are reported for standard test sets that are in common use. The overall accuracy of SCC-DFTB and the other methods is in the same range, with the overall tendency AM1相似文献   

Copper and iron interactions with angiotensin-converting enzyme inhibitors. A study by fast-atom bombardment tandem mass spectrometry

Fast atom bombardment, combined with high-energy collision-induced tandem mass spectrometry, has been used to investigate gas-phase metal-ion interactions with captopril, enalaprilat and lisinopril, all angiotensin-converting enzyme inhibitors.Suggestions for the location of metal-binding sites are presented. For captopril, metal binding occurs most likely at both the sulphur and the nitrogen atom. For enalaprilat and lisinopril, binding preferably occurs at the amine nitrogen. Copyright 1999 John Wiley & Sons, Ltd.     

A comparative study on the separation of radioyttrium from Sr- and Rb-targets via ion-exchange and solvent extraction techniques,with special reference to the production of no-carrier-added <Superscript>86</Superscript>Y, <Superscript>87</Superscript>Y and <Superscript>88</Superscript>Y using a cyclotron

The radiochemical separation of ⁸⁸Y from proton irradiated ^natSrCO₃ and alpha-particle irradiated ^natRbCl, of ⁸⁶Y from proton irradiated ⁸⁶SrCO₃, and of ⁸⁷Y from alpha-particle irradiated ^natRbCl were studied at no-carrier-added levels by two techniques, namely, ion-exchange chromatography using Dowex 50W-X8 and Dowex 21K resins, and solvent extraction using HDEHP. Out of all those methods, the ion-exchange chromatography using Dowex 50W-X8 (cation-exchanger) was found to be the best: the separation yield was high, the chemical impurity in the separated radioyttrium (inactive Sr or Rb) was low (0.5 μg) and the final product was obtained in the form of citrate. The optimized separation method using Dowex 50W-X8 was applied in practical production of ⁸⁶Y and ⁸⁸Y via proton irradiations of ⁸⁶SrCO₃ and ^natSrCO₃, respectively, at 16 MeV as well as of ⁸⁷Y and ⁸⁸Y via α-particle irradiation of ^natRbCl at 26 MeV. The tangible experimental yields of ⁸⁶Y and ⁸⁷Y amounted to 150 and 5.7 MBq/μA·h, respectively. The yields of ⁸⁸Y obtained were 0.06 MBq/μA·h and 1 MBq/μA·h for alpha-particle and proton irradiations, respectively. Each yield value corresponds to more than 70% of the respective theoretical value.     

Atom-scale ptychographic electron diffractive imaging of boron nitride cones

Ptychographic coherent diffractive imaging (CDI) has been extensively applied using both x rays and electrons. The extension to atomic resolution has been elusive. This Letter demonstrates ptychographic electron diffractive imaging at atomic resolution, permitting identification of structure in a boron nitride helical cone at a resolution of order 1 ?, beyond that of comparative Z-contrast images. A scanning transmission electron microscope is used to create a diverging illumination in a defocused Fresnel CDI geometry, providing a robust strategy leading to a unique solution.     

Collective characteristics of hadron systems produced in beam fragmentation of π+ p collisions at 250 GeV/c

Collective characteristics are studied of hadrons produced in beam fragmentation of non-single-diffractive π⁺ p-interactions at 250 GeV/c. An attempt is made to obtain experimental information on the properties of leading cluster production and fragmentation. On average, the leading cluster carries 0.8±0.1 of the incident momentum, so that the mean value of the inelasticity coefficient of 〈k〉=0.2±0.1 is significantly smaller than that deduced from leading single hadron spectra. The momentum transfer distribution shows that nonsingle-diffractive processes are less peripheral than diffraction dissociation. The analysis of thrust and sphericity shows jet-like structure of pion fragmentation, that of the charge flow an average forward charge of 〈Q _f 〉=0.45±0.04, in agreement with the average charge of the beam valence quarks. Our data are compared to diffraction dissociation and to the Fritiof model.