Transverse josephson plasma mode in T* cuprate superconductors

A transverse optical plasma mode is observed at far-infrared frequencies within the superconducting gap region by measuring the c-axis optical reflectivity for single crystals of T* cuprate superconductors SmLa0.85Sr0.15CuO4-delta and Nd1.4Sr0.4Ce0.2CuO4-delta. These T* cuprates have two different insulating layers sandwiching the superconducting CuO2 planes, leading to two longitudinal plasmons. Also, the transverse mode is directly observed due to the coupling of the infrared radiation with the current perpendicular to the superconducting layers which are regarded as an alternating array of two inequivalent Josephson junctions.     

Infrared femtosecond laser pulse induced permanent reduction of Eu3+ to Eu2+ in a fluorozirconate glass

We report what is believed to be the first observation of permanent photoreduction of Eu(3+) to Eu(2+) in transparent and colorless Eu(3+) -doped fluorozirconate glass at room temperature, using an infrared femtosecond laser. Difference absorption and electron-spin-resonance spectra of the glass before and after laser irradiation showed that a portion of the Eu(3+) ions in the focused part of the laser inside the glass were reduced to Eu(2+) ions after laser irradiation. It is suggested that Eu(3+) ions act as electron-trapping centers, whereas active sites in the glass matrix act as hole-trapping centers, leading to the formation of Eu(2+) ions. The observed phenomenon is inferred to be useful in the fabrication of optical memory devices with high storage density and waveguide-type micro-optical devices.     

New dissipation relaxation phenomenon in oscillating solid (4)He

We describe the first observations on the time-dependent dissipation when the drive level of a torsional oscillator containing solid (4)He is abruptly changed. The relaxation of dissipation in solid (4)He shows rich dynamical behavior including exponential and logarithmic time-dependent decays, hysteresis, and memory effects.     

A Mechanistic Dichotomy in Two-Electron Reduction of Dioxygen Catalyzed by N,N’-Dimethylated Porphyrin Isomers

Selective two-electron reduction of dioxygen (O₂) to hydrogen peroxide (H₂O₂) has been achieved by two saddle-distorted N,N’-dimethylated porphyrin isomers, an N21,N’22-dimethylated porphyrin ( anti -Me₂P ) and an N21,N’23-dimethylated porphyrin ( syn -Me₂P ) as catalysts and ferrocene derivatives as electron donors in the presence of protic acids in acetonitrile. The higher catalytic performance in an oxygen reduction reaction (ORR) was achieved by anti -Me₂P with higher turnover number (TON=250 for 30 min) than that by syn -Me₂P (TON=218 for 60 min). The reactive intermediates in the catalytic ORR were confirmed to be the corresponding isophlorins ( anti -Me₂Iph or syn -Me₂Iph ) by spectroscopic measurements. The rate-determining step in the catalytic ORRs was concluded to be proton-coupled electron-transfer reduction of O₂ with isophlorins based on kinetic analysis. The ORR rate by anti -Me₂Iph was accelerated by external protons, judging from the dependence of the observed initial rates on acid concentrations. In contrast, no acceleration of the ORR rate with syn -Me₂Iph by external protons was observed. The different mechanisms in the O₂ reduction by the two isomers should be derived from that of the arrangement of hydrogen bonding of a O₂ with inner NH protons of the isophlorins.     

Discrete π Stack of a Tweezer-Shaped Naphthalenediimide–Anthracene Conjugate

The design and synthesis of a tweezer-shaped naphthalenediimide (NDI)–anthracene conjugate ( 2NDI ) are reported. In the structure of the closed form (π_NDI ⋅⋅⋅ π_NDI stack) of 2NDI , which was elucidated by single-crystal XRD, the existence of C−H ⋅⋅⋅ O hydrogen bonding involving the nearest carbonyl oxygen atom of an NDI unit was suggested. The tunability of π_NDI ⋅⋅⋅ π_NDI interactions was studied by means of UV/Vis absorption, fluorescence and NMR spectroscopy and molecular modelling. This revealed that the π_NDI ⋅⋅⋅ π_NDI interactions in 2NDI affect the absorption and emission properties depending on the temperature. Furthermore, in polar solvents, 2NDI prefers the stronger π_NDI ⋅⋅⋅ π_NDI stack, whereas the π_NDI ⋅⋅⋅ π_NDI interaction is diminished in nonpolar solvents. Importantly, the conformational variations of 2NDI can be reversibly switched by variation in temperature, and this suggests potential application for fluorogenic molecular switches upon temperature changes.     

Interaction and arrangement of nitrogen and carbon atoms in fcc γ-iron

A Mössbauer effect measurement has been done for Fe?N, Fe?Al?C and Fe?Ni?C austenite in order to study the interaction between the interstitial atoms and their distribution among the octahedral sites of the fcc lattice, together with the influence of Al and Ni atoms. The spectra for Fe?N and Fe?Al?C austenite are decomposed into three components; one singlet γ₀, and two sets of doublet γ₁ and γ₂, with different quadrupole splittings, while no γ₂ component is found in the spectrum for Fe?Ni?C. By analyzing the component ratio in each spectrum, it is concluded that, in Fe?N and Fe?Al?C, the interaction between 2nd nearest neighboring nitrogen or carbon atoms is attractive, and is repulsive between 1st nearest for Fe?N, and that the interaction between 2nd nearest atoms is repulsive for Fe?Ni?C. By measuring the spectra of Fe?Ni?C in magnetic field, the sign of EFG for most of the γ₁ component is determined to be negative.     

Analysis of dislocation images in X-ray topography of protein crystals: tetragonal hen egg-white lysozyme crystals

Dislocation images in X-ray topography of protein crystals such as tetragonal hen egg-white lysozyme crystals were analyzed. Not only extinction but also double contrast of dislocation images are clearly observed on the X-ray topographs. It should be noted that the observed image widths of the dislocation contrasts are much less than those calculated on the basis of the kinematical theory in X-ray topography, which has been successfully applied for inorganic crystals and organic crystals of small molecules so far. Moreover, in tetragonal HEW lysozyme crystals, the rocking curve widths of the perfect crystal related to the kinematical theory are less than the measured ones by two orders of magnitude. This discrepancy is consistent with that in the image width of the dislocation contrast. From this correlation, it is suggested that the larger rocking curve width, or higher mosaicity, is mainly responsible for the observed image width in the grown crystals.