Contribution of conformational change of polymer structure to electrochemomechanical deformation based on polyaniline

The pH dependencies of electrochemomechanical deformation (ECMD) including the cyclic voltammetry and the expansion ratio in conducting polymers, polyaniline (PANI), and poly(o-methoxyaniline) film were studied to elucidate the mechanisms. It was found that the ECMD is governed by the conformational change of polymer structure as well as the insertion of bulky ions in the manner of comparable magnitude. Expansion ratios >20% in the ECMD were demonstrated for the thickness direction of PANI film. The results suggest that the magnitude of ECMD can be improved by choosing the preparation method of films.     

Voltammetric studies of antimony ions in soda-lime-silica glass melts up to 1873 K.

The half wave potential of reduction of Sb5+ in 16Na2O x 10CaO x 74SiO2 glass melts was examined by differential pulse voltammetry up to 1873 K. The half wave potential shifted to the positive direction with an increase in temperature. The results indicate that the equilibrium of Sb5+/Sb3+ shifted to negative direction with an increase in temperature. The half wave potential shifted to positive direction (48 mV at 1473 K) when the atmosphere over the melts changed from pure oxygen gas to air, in agreement with the theoretical prediction. The reversibility of Pt:O2 reference electrode is confirmed.     

Isotope-dependent crystalline phases at ambient temperature: Spectroscopic and calorimetric evidence for a deuteration-induced phase transition at 320 K in α-DCrO2

The heat capacities of HCrO₂ and DCrO₂ have been measured at temperatures between 5 and 360 K. A lambda anomaly occurred at 320 K for DCrO₂ but not for HCrO₂. Infrared spectra were recorded at temperatures between 5 and 405 K. The spectrum of DCrO₂ changed at 320 K with respect to the peak wave-number and splitting of some of the vibrations, while those of HCrO₂ depended smoothly on temperature. These experimental results are discussed in terms of a deuteration-induced phase transition.     

Selective and efficient transformation of N-(4-substituted benzoyl)-α-dehydroarylalanine alkyl esters into 4,5-dihydrooxazole derivatives via photoinduced electron transfer

The irradiation of N-(4-substituted benzoyl)-α-dehydroarylalanine alkyl esters (1) in methanol containing triethylamine (TEA) was found to quantitatively give cis- and trans-4,5-dihydrooxazole derivatives (2), which were described as being formed via electron transfer from TEA to the excited-state (E)-1 followed by kinetically-controlled cyclization of the (E)-1-derived anion radical. A product composition analysis showed that the cis-2/trans-2 composition ratio is greatly varied depending on the stereoelectronic properties of the substituents, the polarity of protic solvents and the concentration of TEA.     

Electronic state of a CoO2 layer with hexagonal structure: a Kagomé lattice structure in a triangular lattice

The electronic state in layered cobalt oxides with a hexagonal structure is examined. We find that the electronic structure reflects the nature of the Kagomé lattice hidden in the CoO2 layer which consists of stacked triangular lattices of oxygen ions and of cobalt ions. A fundamental model for the electron system is proposed, and the mechanism of the unique transport and magnetic properties of the cobalt oxides are discussed in light of the model.     

Synthesis and evaluation of 6-nitro-7-(1-piperazino)quinazolines: dual-acting compounds with inhibitory activities toward both tumor necrosis factor-alpha (TNF-alpha) production and T cell proliferation

We investigated the chemical modifications of the nitroquinazoline derivative (1) through the replacement of the NH group at the C(4)-position with several N-alkyl groups to increase the lipophilicity at the C(4)-position. Among them, we found that the N-methyl analogue (5a) showed a 2-fold loss in the inhibitory activity toward tumor necrosis factor-alpha (TNF-alpha) production in vitro as compared with the NH analogue (1); however, 5a exhibited an oral inhibitory activity on TNF-alpha production with an ED50 value of 26 mg/kg, whereas 1 did not. Moreover, the oral bioavailability of 5a was higher than that of 1 (1, F=1%; 5a, F=21%), and the calculated ClogP value for 5a was higher than that for 1. These results suggest that the improved lipophilicity of 5a compared with that of 1 reflects its greater inhibitory activity on TNF-alpha production in vivo as well as oral bioavailability.     

Doppler-shifted cyclotron absorption of electron Bernstein waves via N( parallel)-upshift in a Tokamak plasma

Extraordinary (X) waves are perpendicularly injected for electron Bernstein (B) wave heating into an Ohmically heated plasma from the inboard side in the WT-3 tokamak. Measurements show that absorption does not take place at the electron cyclotron resonance layer nor the upper hybrid resonance layer, but does happen midway between them. This is consistent with the ray tracing prediction, i.e., the poloidal field and poloidal inhomogeneity of toroidal field lead the B waves to have a large parallel refractive index N( parallel) (>1), and the B waves are damped away via the Doppler-shifted cyclotron resonance.