Synthesis of a C3-symmetric tris-imine via dynamic covalent bond formation between a trialdehyde and a triamine

Dynamic covalent chemistry is an effective technique for the preparation of complex organic compounds. We succeeded in synthesizing a cage-shaped compound through the aggregation of two types of functional molecules. More specifically, a tris-imine 5 was quantitatively obtained by reacting a C₃-symmetric trialdehyde 1 with a triamine 4 in acetonitrile in the presence of a trifluoroacetic acid catalyst. We also achieved the synthesis of the corresponding triamine 9 and the acetylated derivative 10 through reduction of the tris-imine CN double bonds and subsequent acetylation.     

238U Mössbauer study on the magnetic properties of uranium-based heavy fermion superconductors

We have performed ²³⁸U Mössbauer spectroscopy of uranium-based heavy fermion superconductors, UPd₂Al₃ and URu₂Si₂, in order to investigate their physical properties, mainly their magnetic properties. The slow relaxation of magnetic hyperfine interaction in a paramagnetic state and the static hyperfine field has been observed in an antiferromagnetic ordered state for each compound. The line-widths have maximum at their characteristic temperatures where their magnetic susceptibilities have maximum values.     

Signal Formation of Image-Edge Motion Based on Biological Retinal Networks and Implementation into an Analog Metal-Oxide-Silicon Circuit

A simplified model was proposed for the formation of edge signals and generation of motion signals of a target based on the information processing mechanisms of outer and inner retinas of a vertebrate. Analog metal-oxide-silicon (MOS) integrated circuits were designed based on the model. Simulation program with integrated circuit emphasis (SPICE) simulation results showed the performance of local adaptation over a wide dynamic range in the outer retinal circuit and generation of the velocity signal of a moving edge in the inner retinal circuit. Preliminary experimental results showed local adaptation in a given input range in the outer retinal circuit and the generation of motion pulsed signals in the inner retinal circuit.     

Effect of light/dark cycle on bacterial hydrogen production by Rhodobacter sphaeroides RV

Hydrogen production by photosynthetic bacteria provides an efficient energy conversion method under low light intensity. However, under strong illumination, such as midday sunlight, the efficiency drops. This prevents the method from being applied industrially. To overcome this problem, we examined a method to thin out the excessive illumination. Light was given intermittently to reduce the total energy flux. The on/off ratio was set at 1/1 throughout the study, so that the time average of the light energy flux became half the continuous illumination. By keeping the time-average light flux constant (0.6 kW·m⁻²), the effects of the cycle period were examined in the range of hours to seconds. The hydrogen production rate was greatly affected by the cycle period, but cell growth and substrate consumption rates remained almost constant. The 30-min light/dark cycle (30 min on and 30 min off) provided the highest rate of hydrogen production (22 L·m⁻²·24 h⁻¹). At the shorter cycles, the rate decreased except that there was a suboptimum at about 40 s. Under excessive light intensity (1.2 kW·m⁻²), the light-to-hydrogen conversion efficiency was greatly enhanced. The hydrogen production rate during the 30-min cycle was twice as high as during a 12-h cycle under the same conditions.     

Synthesis of neptunyl(VI) hydroxides and their237Np Mössbauer spectra

Four types of neptunyl(VI) hydroxides have been synthesized by chemical oxidation of Np(IV) instead of ozone oxidation of Np(V) which caused the partial oxidation to the heptavalent state. NpO₂(OH)₂ (I) and NpO₂(OH)₂·H₂O (orthorhombic type) (II) have been obtained by adding pyridine to the solution at 373K and 343K, respectively. NpO₂(OH)₂·H₂O (hexagonal type) (III) and NpO₂(OH)₂·xH₂O·yNH₃ (x+y=1) (IV) have been prepared by using LiOH and NH₄OH, respectively. The four materials have been characterized by X-ray powder diffraction patterns, thermogravimetric analysis and²³⁷Np Mössbauer spectra. The²³⁷Np Mössbauer spectrum of (I) measured first time as anhydrous neptunyl(VI) hydroxide (δ=?46.2 mm/s,e ² qQ=193 mm/s and η=0.16 at 4.8K) has more distinct five-line Mössbauer pattern than those of (II), (III) and (IV). The Mössbauer spectra for (II), (III) and (IV) are slightly different from each other. The structural information has been obtained from these data.     

Two-particle rapidity correlations in αα, αp,andp p interactions at the CERN intersecting storage rings

Two-particle rapidity correlations have been studied for αα, αp, andp p interactions at the CERN ISR using the Split-Field Magnet (SFM) detector. In order to isolate the true two-particle correlations, the analysis was performed at fixed charged multiplicity. In the framework of a simple cluster model, it is found that cluster widths as well as cluster multiplicities are the same for αα, αp, andp p interactions, and both decrease with increasing charged multiplicity.     

Status of the LHCb experiment

The European Physical Journal C - LHCb is a dedicated experiment to study CP violation and other rare processes in the B meson system at LHC. It is designed to exploit the large sample of Bd and Bs...     

Effective dephosphorylation catalyzed by fluoride ion: A novel synthesis of terminal f-alkylacetylenes from f-alkanoyl chlorides

1H-F-Alkene-1-phosphonates, easily accessible from F-alkanoyl chlorides, underwent dephosphorylation on treatment with a catalytic amount of fluoride ion at O°C to room temperature to give terminal F-alkylacetylenes in good yields.     

Synhtesis of 2-ethoxy-6,11-dimethyl-7,9-bisdehydroaza[16]annulene and 2-ethoxy-8,13-dimethyl-9,11-bisdehydroaza[18]annulene

Title azaannulenes, the paratropic and diatropic vinylogues of pyridine, were synthesized starting from the annulenones.     

237Np Mössbauer spectroscopic study on heptavalent neptunium compound

²³⁷Np Mössbauer spectrum of the heptavalent neptunium compound [Co(NH₃)₆][NpO₄(OH)₂]·2H₂O was remeasured for certification of the previous investigations. The isomer shift value of the Mössbauer spectrum showed a characteristic value for the heptavalent neptunium at 4.7K. Although the spectrum seemed to consist of two quadrupole-split peaks as previously reported byStone et al., the fitting with using two quadrupole-split peaks did not give a good agreement withStone's data.