Avenic acid,a new amino acid possessing an iron chelating activity

A new amino acid derivative possessing an iron chelating activity was isolated from root washings of water cultured $\text{Avena sativa}$ under iron deficient conditions. The structure of this compound, avenic acid A has been determined as 2(S),3′(S),3″(S)-N-[3-(3-hydroxy-3-carboxypropylamino)-3-carboxypropyl]-homoserine (1) on the basis of chemical and spectroscopic evidence.     

Cycloaddition reaction of pyrimidine-dienols with dienophiles. A new approach to quinazolines

A new synthetic approach to quinazolines bearing a carboxy group is described. Reaction of 5-carbonyl substituted 1,3,6-tri-methyluracils (I) with dimethyl acetylenedicarboxylate or electron-deficient olefines affords quinazoline derivatives (III-VI) $\text{via}$ pyrimidine(Z)-dienols (II) formed by base-catalyzed isomerization.     

Infrared spectroscopic studies of polymer transitions. III. Effects of sodium ion on glass transitions in styrene-based ionomers

The glass transition in styrene-based ionomers was investigated by means of infrared spectroscopy and differential scanning calorimetry (DSC). Transition temperatures were determined from the temperature dependence of the peak absorbances of the 1700 and 1745 cm^?1 bands. These transition temperatures agreed with glass transition temperatures (T_g) determined by DSC. With increasing degree of ionization, T_g and the enthalpy ΔH of the residual intermolecular hydrogen bonding increased. The values of T_g obtained were analyzed by the theory of Fox and Loshaek for the effect of crosslinks. It is concluded that sodium ions probably from ionic domains and act as crosslinks to reinforce the residual hydrogen bonding and may increase T_g. The absorbance at 1560 cm^?1 (ν_COO^?) did not change at T_g. This suggests that the glass transition observed here is not due to the onset of the mobility in ionic domains, as has been proposed for ethylene-based ionomers on the basis of dielectric measurements.     

Selective absorption

Summary Some organic acids, alcohol and amine which have an asymmetric carbon atom were used for an investigation of asymmetric absorption on wool. Racemic mixture of hydratropic acid, mandelic acid andα-phenethylamine have shown the selective absorption on wool from their aqueous and alcoholic aqueous solutions and S-form of their diastereoisomers preferentially absorbed on wool. According to the results we obtained so far, it is concluded that the preferential absorption strongly depends on the configuration of the substance of which wool is composed.     

Excitation migration among inhomogeneously broadened levels of Eu3+ ions

Excitation migration between ⁵D₀ states of Eu³⁺ ions in Ca(PO₃)₂ glass is studied by using the technique of the selective excitation of the inhomogeneously broadened ⁵D₀ levels. In time-resolved emission spectra for ⁵D₀→⁷F₁ transition after the pulse excitation due to ⁷F₀→⁵D₀ transition by the use of a tunable dye laser at 77°K, a subpeak is observed to appear and to grow in intensity with increasing delay time, besides the main peak excited directly by the excitation light. The observed facts are explained by considering the phonon-assisted energy transfer between ⁵D₀ states involving an acoustic phonon. From the analysis of the results, the probability of the excitation migration due to the phonon-assisted process is estimated to be ≌ 10 A ms^-1. From the theoretical consideration, the rate of the linewidth change and the probability of the excitation migration due to the resonant transfer process are obtained. These results indicate that the phonon-assisted process is more dominant than the resonant process for the excitation migration in the system studied.     

Anisotropic excitonic molecules in CdS and CdSe

Luminescence lines due to excitonic molecules are observed in CdS and CdSe. The line shape is analyzed by taking account of the broadening due to elastic collision. It is pointed out that the anisotropy of the effective hole masses makes the molecular binding energies much larger than evaluated by using the geometrical means of the hole masses.     

A New Type of Photorearrangement of γ-Hydroxy-α, β, δ, ε-dienone

A new type of photorearrangement of the γ-hydroxy-α, β, δ, ε-dienone, vomifoliol acetate ( 2 ) to the diketone 4 is described, and its facile rearrangement is compared with that of desoxyvomifoliol acetate ( 3 ).     

Development of high-radiation-sensitive polymer gel for magnetic resonance imaging in three-dimensional dosimetry

We developed a high radiation sensitive polymer gel by modifying the amounts of the gel components and the temperature for the gel preparation. We evaluated its relaxation time linearity against dose and compared the measured dose distribution with the calculated one. For the relaxation time-dose linearity, irradiations were carried out with a linear accelerator using 6 MV photons and doses ranging from 0-5.0 Gy. The relationship between dose and R(2) value (reciprocal of T(2) relaxation time) was measured and it had good linearity over a wide range (0.3-5 Gy). The measured dose distributions were in good agreement with calculated ones. Since the present gel has higher sensitivity and it is synthesized more easily at lower cost than conventional polymer gels, we expect to see improved three-dimensional (3D) dosimetry using it.     

Specific heat measurement of the layered nitride superconductor Li(x)ZrNCl

Specific heat has been investigated in a layered nitride superconductor, Li(0.12)ZrNCl, with T(c)=12.7 K. The obtained data have shown a marked dichotomy: The specific heat jump at T(c) (DeltaC/gamma(n)T(c)=1.8) and the superconducting gap ratio (2Delta/k(B)T(c)=4.6-5.2) have indicated an intermediate to a strong coupling of electrons, while the upper limit of the electron-phonon coupling constant lambda has directly been estimated to be 0.22, which belongs to a weak coupling regime. Furthermore, the rapid increase of gamma as a function of magnetic field suggests that the present material has an anisotropic s wave gap.