Absolute and convective instabilities of electrostatic ion cyclotron waves excited in an ion beam-plasma system

Experimental results are presented for the observation of the absolute and convective instabilities of the electrostatic ion cyclotron waves excited in an ion beam-plasma system.     

Highly Asymmetrical Porphyrins with Enhanced Push–Pull Character for Dye‐Sensitized Solar Cells

A porphyrin π‐system has been modulated by enhancing the push–pull character with highly asymmetrical substitution for dye‐sensitized solar cells for the first time. Namely, both two diarylamino moieties as a strong electron‐donating group and one carboxyphenylethynyl moiety as a strong electron‐withdrawing, anchoring group were introduced into the meso‐positions of the porphyrin core in a lower symmetrical manner. As a result of the improved light‐harvesting property as well as high electron distribution in the anchoring group of LUMO, a push–pull‐enhanced, porphyrin‐sensitized solar cell exhibited more than 10 % power conversion efficiency, which exceeded that of a representative highly efficient porphyrin (i.e., YD2)‐sensitized solar cell under optimized conditions. The rational molecular design concept based on highly asymmetric, push–pull substitution will open the possibilities of further improving cell performance in organic solar cells.     

O- and N-Glycosidation of d-glycals using Ferrier rearrangement under Mitsunobu reaction conditions. Application to N-nucleoside synthesis

We have disclosed the reaction of 3-hydroxy free glycals with O- or N-nucleophiles under Mitsunobu reaction conditions proceeded to produce 2,3-unsaturated glycosides in good to high yield and moderate stereoselectivity. The reaction would take place via allyloxycarbenium ion.     

Three p‐xylene‐solvated pseudopolymorphs of bis[1,3‐bis(pentafluorophenyl)propane‐1,3‐dionato]copper(II)

The Cu²⁺ ions in the title compounds, namely bis[1,3‐bis(pentafluorophenyl)propane‐1,3‐dionato‐κ²O,O′]copper(II) p‐xylene n‐solvate, [Cu(C₁₅HF₁₀O₂)₂]·nC₈H₁₀, with n = 1, (I), n = 2, (II), and n = 4, (III), are coordinated by two 1,3‐bis(pentafluorophenyl)propane‐1,3‐dionate ligands. The coordination complexes of (I) and (II) have crystallographic inversion symmetry at the Cu atom and the p‐xylene molecule in (I) also lies across an inversion centre. The p‐xylene molecules in (I) and (II) interact with the pentafluorophenyl groups of the complex via arene–perfluoroarene interactions. In the crystal of (III), two of the p‐xylene molecules interact with the pentafluorophenyl groups via arene–perfluoroarene interactions. The other two p‐xylene molecules are located on the CuO₄ coordination plane, forming a uniform cavity produced by metal...π interactions.     

Thermodynamic properties of successive phase transitions in Rb2ZnBr4

Heat capacity measurements have given the following transition temperatures and entropies: 0.027 J K^?1mol^?1 at 76.5 K, 0.47 J K^?1mol^?1 at 111.7 K, and 0.048 J K^?1mol^?1 at 193.6 K. These are interpreted as “lock-in”, soft-mode, and “lock-in” transitions, respectively, from comparison with analogous results for Rb₂ZnCl₄ and K₂SeO₄. The N-IC transition was located at 347 K by DTA.     

Systemically Injectable Enzyme‐Loaded Polyion Complex Vesicles as In Vivo Nanoreactors Functioning in Tumors

The design and construction of nanoreactors are important for biomedical applications of enzymes, but lipid‐ and polymeric‐vesicle‐based nanoreactors have some practical limitations. We have succeeded in preparing enzyme‐loaded polyion complex vesicles (PICsomes) through a facile protein‐loading method. The preservation of enzyme activity was confirmed even after cross‐linking of the PICsomes. The cross‐linked β‐galactosidase‐loaded PICsomes (β‐gal@PICsomes) selectively accumulated in the tumor tissue of mice. Moreover, a model prodrug, HMDER‐βGal, was successfully converted into a highly fluorescent product, HMDER, at the tumor site, even 4 days after administration of the β‐gal@PICsomes. Intravital confocal microscopy showed continuous production of HMDER and its distribution throughout the tumor tissues. Thus, enzyme‐loaded PICsomes are useful for prodrug activation at the tumor site and could be a versatile platform for enzyme delivery in enzyme prodrug therapy.     

Internal-friction study of the interstitial–substitutional effect on the deformation behaviour of Nb–O,Nb–Ta–O and Nb–Mo–O single crystals

To investigate the interstitial-substitutional interaction in dislocations, the effect of 0 on the temperature, frequency and amplitude dependence of the internal friction Q ^?1 in Nb–O, Nb-20 mol% Ta–O and Nb-20 mol% Mo–O single crystals has been studied (f = 1.55–8.2 Hz) in the temperature range from 298 to 1473 K. In our previous study, Nb–Mo and Nb–Ta single crystals were found to be strengthened by solute O. It was also suggested that the interstitial–substitutional interaction in dislocations contributes to the increase in their critical resolved shear stress (CRSS). In this study, Snoek-type relaxation peaks due to O are observed between 500 and 700 K in all the single crystals. The Snoek peak of Nb-20mol% Mo–O consisting of several peaks is analysed. The activation energy of the Snoek peak in Nb-20mol% Mo–O is higher than that of Nb–O. These results are attributable to the existence of the interstitial–substitutional complexes. The amplitude dependence of Q ^?1 at intermediate and high temperatures decreases as the O content increases. Moreover, the breakaway stress of Nb-20 mol% Mo–O still has a high value at 1200K and does not decrease much even at 1473 K. This suggests that the formation of Mo–O complexes reduces the dislocation mobility at high temperatures. From the results, the effect of the interstitial-substitutional interaction on the CRSS was discussed.     

Accurate determination of the number density of G-phase precipitates in thermally aged duplex stainless steel

G-phase precipitation in the ferrite phase in thermally aged duplex stainless steel (DSS) was investigated. A needle-shaped sample of DSS aged at 673?K for 5000?h was observed by transmission electron microscopy (TEM), and subsequently by atom probe tomography (APT). The precipitates of the G-phase observed by TEM corresponded well to clustering atoms observed by APT. On the other hand, regarding the precipitates of the G-phase that formed in an earlier stage of aging, the present study suggests that not all the precipitates can be detected by TEM. A large area of DSS aged at 673?K for 5000?h containing both the ferrite and austenite phases was observed. The number density of precipitates of the G-phase in the ferrite phase was small in the vicinity of the phase boundary and increased with the distance between the phase boundary and each field of view. The number density reached an almost constant value at a distance of approximately 4?µm from the phase boundary. The suppression of G-phase precipitation in the vicinity of the phase boundary is discussed in terms of the depletion of alloying elements that comprise the G-phase.