A study of 75Se by neutron capture and the SU(3)-SU(5) transition in the quadrupole-phonon representation

The γ and e^? spectra following thermal neutron capture in ⁷⁴Se were studied with curved-crystal, β, and pair spectrometers. Precise energies have been obtained for the transitions and levels at low energies. Two primary E2 transitions were found. The neutron separation energy for ⁷⁵Se was determined as 8027.6 keV. Precise γ-energies following the electron capture decay of ⁷⁵Se were also measured, resulting in precise level energies in ⁷⁵As. The calculation of the energy levels in ⁷⁵Se has been performed in the SU(6) particle-vibrational model (PTQM) and 27 theoretical states have been tentatively assigned to the experimental levels. The spectrum of the core nucleus ⁷⁴Se has been calculated in the SU(6) quadrupolephonon model (TQM). The structure of theoretical states, the relation to SU(3) and SU(5) limits, and potential energy surface are discussed. The E2, M1 and E1 transitions have been calculated in PTQM and compared to the experiment. Also, an overview is presented of theoretical explanations of the I = j, j?1, j?2 anomalous triplet emphasizing the rule with shell-model classification corrected for quadrupole phonons.     

Ring beam shaping optics fabricated with ultra-precision cutting for YAG laser processing

In this study, a method for generating ring intensity distribution at a refraction-type lens with an aspheric element was proposed, and the beam shaping optical element was finished using only ultra-precision cutting. The shape of the optical element and its irradiance pattern were determined from numerical calculation based on its geometrical and physical optics. An ultra-precision lathe was employed to fabricate beam shaping optical elements, and acrylic resin was used as the material. The transmittance of an optical element (a rotationally symmetrical body) with an aspheric surface fabricated using a single-crystal diamond tool was over 98%, and its surface roughness was 9.6 nm Ra. The method enabled the formation of a circular melting zone on a piece of stainless steel with a thickness of 300 μm through pulse YAG laser (λ 1:06 μm) processing such that the average radius was 610 μm and the width was 100–200 μm. Circular processing using a ring beam shaping optical element can be realized by single-pulse beam irradiation without beam scanning.     

Vibronic coupling in benzene cation and anion: vibronic coupling and frontier electron density in Jahn-Teller molecules

Vibronic coupling constants of Jahn-Teller molecules, benzene radical cation and anion, are computed as matrix elements of the electronic part of the vibronic coupling operator using the electronic wave functions calculated by generalized restricted Hartree-Fock and state-averaged complete active space self-consistent-field methods. The calculated vibronic coupling constants for benzene cation agree well with the experimental and theoretical values. Vibronic coupling density analysis, which illustrates the local properties of the coupling, is performed in order to explain the order of magnitude of the coupling constant from view of the electronic and vibrational structures. This analysis reveals that the couplings of the e2g2 and e2g3 modes in which the large displacements locate on C-C bonds are strong in the cation. On the other hand, they are greatly weakened in the anion because of the decrease of electron density in the region of the C-C bonds, which originates from the antibonding nature of the singly occupied molecular orbital of the anion. However, the difference of the electronic structure has a little influence on the vibronic coupling of the e2g4 mode. These results indicate that the vibronic coupling depends not only on the direction of the nuclear displacement but also on the frontier electron density.     

Synthesis and pharmacological profile of an orally-active growth hormone secretagogue, SM-130686

Hypothalamic hormones physiologically regulate pulsatile release of growth hormone (GH) from the anterior pituitary gland. Since the discovery of these hormones in the 1970s, several new chemically synthesized peptidyl and non-peptidyl derivatives have been proved to stimulate and amplify GH secretion, and this series of molecules has been named the growth hormone secretagogues (GHSs). One of these compounds led to the discovery of a GPCR-type receptor for GHSs (GHS-R), and subsequently the endogenous ligand for the receptor has been identified, and is referred to as ghrelin. The identification of GHSs as physiological regulators of GH secretion encouraged us to examine our GHSs pharmacologically. We previously reported that novel oxindole derivatives have been identified as GHS-R agonists from our internal chemical library. Among these derivatives, (+)-6-carbamoyl-3-(2-chlorophenyl)-(2-diethylaminoethyl)-4-trifluoromethyloxindole (SM-130686, 37S) was found to have potent activity in vitro with a good pharmacokinetic profile in rats (bioavailability of 28%). In this article, we review the synthesis and pharmacological evaluation of SM-130686. SM-130686 binds specifically to GHS-R and increases the Ca(2+) concentration in Chinese hamster ovary cells expressing recombinant GHS-R. Maximal enhancement of the intracellular Ca(2+) concentration induced by SM-130686 treatment was approximately 55% that induced by ghrelin, suggesting that SM-130686 may be a partial GHS-R agonist. Also, in in vivo studies, oral administration of SM-130686 increased body length and fat-free mass gain. We compare the pharmacological profile of SM-130686 with other GHSs, including GHRH and ghrelin, and discuss the therapeutic usefulness of GHSs against several disorders, as well as for treatment of GH deficiency.     

Disordered ground state and magnetic field-induced long-range order in an S=3/2 antiferromagnetic honeycomb lattice compound Bi3Mn4O12(NO3)

Bi3Mn4O12(NO3), in which the Mn4+ ions carry S=3/2, is the first honeycomb lattice system that shows no long-range magnetic order. Using neutron scattering, we have determined that short-range antiferromagnetic correlations develop at low temperatures. Applied magnetic fields induce a magnetic transition, in which the short-range order abruptly expands into a long-range order.     

Multiferroic M-type hexaferrites with a room-temperature conical state and magnetically controllable spin helicity

Magnetic and magnetoelectric (ME) properties have been studied for single crystals of Sc-doped M-type barium hexaferrites. Magnetization (M) and neutron diffraction measurements revealed that by tuning Sc concentration a longitudinal conical state is stabilized up to above room temperatures. ME measurements have shown that a transverse magnetic field (H) can induce electric polarization (P) at lower temperatures and that the spin helicity is nonvolatile and endurable up to near the conical magnetic transition temperature. It was also revealed that the response (reversal or retention) of the P vector upon the reversal of M varies with temperature. In turn, this feature allows us to control the relation between the spin helicity and the M vectors with H and temperature.     

Preparation and electrochemical behaviour of hydrophobic vitamin B(12) covalently immobilized onto platinum electrode

Hydrophobic vitamin B(12) was covalently immobilized onto a platinum electrode surface, and the immobilized complex exhibits Co(ii)/Co(i) redox couple and in situ the Co(i) species reacts with phenethyl bromide to form styrene under irradiation with visible light with a turnover number of over 6000 for 1 h.