Recent studies of unstable nuclei far from stability with the on-line isotope separators of JAERI

Studies on the decay of unstable nuclei using the two on-line isotope separators of JAERI are reviewed for the past five years. With the previously established ion-source technique using mono-oxide ion formation in a thermal ion source, the new nuclides¹²⁵Pr and¹²⁷Pr have been identified in heavy-ion fusion residues. Further, with a newly developed gas-jet coupled thermal ion source, the new nuclides¹⁶⁶Tb,¹⁶⁵Gd,¹⁶¹Sm and²³⁶Am have been identified by bombarding²³⁸U and²³⁵U targets with a proton or⁶Li beam. Other studies, including off-line experiments, by decay spectroscopy, laser spectroscopy and Mössbauer spectroscopy are described.     

Arsenic Compounds in Zoo- and Phyto-plankton of Marine Origin

Major water-soluble arsenic compounds accumulated in some zoo- and phyto-plankton were identified. Zooplankton were collected at sampling stations in the Sea of Japan by a Norpac net towed from 600 m depth to the surface. Phytoplankton were cultivated under axenic conditions. Water-soluble arsenic compounds were extracted repeatedly from plankton tissues by aqueous methanol. The arsenic compounds in the extracts were analyzed by HPLC–ICP/MS. Among zooplankton analyzed in the present study, two carnivorous species, i.e. Amphipoda ( Themisto sp.) and Sagittoidea ( Sagitta sp.), contained arsenobetaine as the dominant arsenic species. Arsenobetaine was the major species in Euphausiacea ( Euphausia sp.), also. The most abundant arsenic compound in the herbivorous Copepoda species ( Calanus sp.), on the other hand, was an arsenic-containing ribofuranoside with a sulfate ester group, and arsenobetaine was only a minor component. Phytoplankton contained arsenic-containing ribofuranosides apparently in a species-speific manner. The arsenic compounds in zooplankton seem to reflect their feeding habit; i.e. carnivorous species eating zooplankton or other small animals accumulate arsenobetaine, while herbivorous ones eating phytoplankton accumulate arsenic-containing ribofuranosides as major arsenic compounds.     

Reaction of dichlorocarbene with 1-(2,4,6-tri-t-butylphenyl)-1-phosphaallenes

1-(2,4,6-Tri-t-butylphenyl)-1-phosphaallene reacted with dichlorocarbene to give 2-dichloromethylene-1-(2,4,6-tri-t-butylphenyl)-1-phosphirane. The structure was confirmed by X-ray crystal structure analysis. A similar isomerization product was obtained in the reaction of dichlorocarbene with 3-phenyl-1-(2,4,6-tri-t-butylphenyl)-1-phosphaallene.     

Dual-wavelength spectrophotometry: Part VI. Qualitative and quantitative analysis by means of first-derivative spectra

Derivative spectrophotometry has many important applications, e.g. detecting trace chemicals in mixture and analyzing isomers or turbid samples, but such measurements have been difficult instrumentally. The first-derivative spectrum can be recorded easily by using dual-wavelength measurements, if the two wavelengths λ₃ and λ₂ are set very close to each other (usually 1–2 nm apart) and scanned simultaneously. Practical applications of derivative spectra in the analysis of rare earths and phenol mixtures are described.     

Global existence results for Oldroyd-B fluids in exterior domains

In this paper we consider the set of equations describing Oldroyd-B fluids in exterior domains. It is shown that these equations admit a unique, global solution defined in a certain function space provided the initial data and the coupling constant are small enough.     

Interplay of superconductivity and rattling phenomena in beta-pyrochlore KOs2O6 studied by photoemission spectroscopy

The electronic structure near the Fermi level (EF) of the beta-pyrochlore superconductor KOs2O6 is studied using laser-excited ultrahigh-resolution photoemission spectroscopy. The superconducting gap clearly opens across the superconducting transition (Tc=9.6 K), with the strong electron-phonon coupling value of 2Delta(0)/k B Tc>or=4.56. A fitting analysis identifies clear anomalies at Tp=7.5 K in the temperature dependencies of the superconducting gap size and the quasiparticle relaxation lifetime. These anomalies and the fine spectral structures arising from phonons suggest that the existence of the rattling behavior of K ions significantly affects the superconductivity in KOs2O6.     

The syntheses and properties of tricyclic pyrrolo[2,3-d]pyrimidine analogues of S6-methylthioguanine and O6-methylguanine

The syntheses of novel tricyclic pyrrolo[2,3-d]pyrimidine analogues of S6-methylthioguanine are described. The crystal structures and pKa values of these and related O6-methylguanine analogues are reported. All compounds display higher pKa values than O6-methylguanine with the sulfur-containing analogues being the more basic and exhibiting higher stability in aqueous solution. In a standard substrate assay with the human repair protein O6-methylguanine-DNA methyltransferase (MGMT) only the oxygen-containing analogue displayed activity.