First systematic band-filling control in organic conductors

The systematic study of band-filling control for four kinds of organic conductors with various kinds of ground states has succeeded. (1) By partial substitution of (GaCl(4))(-) by (MCl(4))(2-) [M = Co, Zn] in the anion blocking layer of lambda-ET(2)(GaCl(4))(-) [ET = bis(ethylenedithio)tetrathiafulvalene], single crystals of lambda-ET(2)(GaCl(4))(-)(1-x)(MCl(4))(2-)(x) [x = 0.0, 0.05, 0.06] have been obtained. The resistivity at room temperature decreases from 3 Omega cm (x = 0.0) to 0.1 Omega cm (x = 0.06) by doping to the antiferromagnet with an effective half-filled band (x = 0.0). (2) Another 2:1 (donor/anion) salt, delta'-ET(2)(GaCl(4))(-), which is a spin gap material, has been doped as delta'-ET(2)(GaCl(4))(-)(1-x)(MCl(4))(2-)(x) [x = 0.05, 0.14]. The resistivity is lowered from 10 Omega cm (x = 0.0) to 0.3 Omega cm (x = 0.14). For both 2:1 salts, the semiconducting behaviors have transferred to relatively conductive semiconducting ones by doping. (3) As for alpha-type 3:1 salts, the parent material is in a charge-ordering state such as alpha-(ET(+)ET(+)ET(0))(CoCl(4))(2-)(TCE), where the charge-ordered donors are dispersed in the two-dimensional conducting layer. Although the calculation of alpha-ET(3)(CoCl(4))(2-)(TCE) shows a band-insulating nature, and the crystal structure analysis indicates that this material is in a charge-ordering state, the metallic behavior down to 165 K has been observed. With doping of (GaCl(4))(-) to the alpha-system, isostructural alpha-ET(3)(CoCl(4))(2-)(1-x)(GaCl(4))(-)(x)(TCE) [x = 0.54, 0.57, 0.62] have been afforded, where the pattern of the horizontal stripe-type charge ordering changes with an increase of x. (4) By doping (GaCl(4))(-) to the 3:2 gapless band insulator which is isostructural to beta'-ET(3)(MCl(4))(2)(2-) [M = Zn, Mn], the obtained beta'-ET(3)(CoCl(4))(2-)(2-x)(GaCl(4))(-)(x) [x = 0.66, 0.88] shows metallic behavior down to 100 and 140 K, respectively. They are the first metallic states in organic conductors by band-filling control of the gapless band insulator. These systematic studies of band-filling control suggest that the doping to the gapless band insulator with a pseudo-1/2-filled band is most effective.     

Atomic level characterization by synchrotron radiation for the design of high performance catalysts

SPring-8 is the largest third-generation synchrotron radiation facility in the world. Synchrotron radiation is the most powerful light source currently available, especially in the EUV and X-ray regions, and in the research area of catalysis synchrotron radiation offers a very useful analysis method, i.e. XAFS. This spectroscopic investigative technique enables the determination of the chemical states and local structure of the atoms in the specific elements of a sample. Here, we introduce the SPring-8 facility and report how synchrotron radiation XAFS spectroscopy is utilized for the characterization and analysis of catalysts.     

Monte Carlo Simulation of Near Infrared Reflectance Spectroscopy in the Wavelength Range from 1000 nm to 1900 nm

We have calculated the characteristics of reflected near infrared light, which is incident on the skin surface, scattered in the skin tissue and detected, in the wavelength range from 1000 nm to 1900 nm. We have used a Monte Carlo method to calculate the propagation path, the average photon visit depth, the average photon path length, etc. for the cases of short source-detector distances, to which the isotropic scattering approximation cannot be applied. An experiment to validate the simulation results was also conducted using a liquid phantom.     

Nitrogenous synergists induced potentiometric response to metal ions with polymeric liquid membranes containing thenoyltrifluoroacetone as an ionophore.

The effects of nitrogenous synergists on the potentiometric responses to divalent transition metal ions were investigated concerning polymeric liquid membranes containing thenoyltrifluoroacetone (Htta) as an ionophore. The tested synergists were pyridine (py) and 4,4'-dioctyl-2,2'-bipyridyl (C8bpy). The potentiometric responses to metal ions, such as Cd2+, Co2+, Ni2+ and Zn2+, were induced by adding the synergists into the liquid membrane systems. The coexistence of Htta and a synergist was necessary for generating the membrane potential. The tta- anion adsorbed at the liquid membrane/solution interface and the complex formation between the synergist and a given metal ion appeared to participate in preferential uptake of metal ions.     

Evaluation of thermodynamic consistency of isobaric and isothermal binary vapor–liquid equilibrium data using the PAI test II,alcohol + n-alkane, +aromatic, +cycloalkane systems

The thermodynamic consistency of binary vapor–liquid equilibrium data has been examined for 46 binary alcohol + hydrocarbon systems with 310 data sets in total (145 isobaric and 165 isothermal sets) using the PAI test proposed in our previous study. The PAI test permits an overall check of the data by combining three tests: a point test, an area test, and an infinite dilution test. In this work, the PAI test was incorporated with the NRTL equation for fitting data. The results of the PAI test for the vapor–liquid equilibrium data showed that the PAI test was able to strictly select reliable data.     

Lignin: its functions and successive flow

Phenolic lignin-based polymers with structure-variable function have originally been designed, and a process has been developed for synthesizing them directly from native lignins. The key point of the process is to set up two different solvents, which are immiscible each other, for selective modification and separation of lignin and carbohydrates: hydrophobic solvent for hydrophobic lignin and hydrophilic solvent for hydrophilic carbohydrates. The native lignins, three dimensional network polymers, are subjected to selective modifications at the interface between both phases to give linear type polymers (lignophenols) composed mainly of 1,1-bis(aryl)propane type units, almost quantitatively. The process provides a new system for successively utilizing lignocellulosics in the molecular level.     

Stochastic orders and their applications in financial optimization

Stochastic orders and inequalities are very useful tools in various areas of economics and finance. The purpose of this paper is to describe main results obtained so far by using the idea of stochastic orders in financial optimization. Especially, the emphasis is placed on the demand and shift effect problems in portfolio selection. Some other examples, which are not related directly to optimization problems, are also given to demonstrate the wide spectrum of application areas of stochastic orders in finance.     

Cation-sensitive fluorescence of anionic polymers bearing naphtho-18-crown-6 units

Changes in the fluorescence intensity of anionic polymers bearing naphtho-18-crown-6 moieties on addition of cations were studied in water at 30 °C. On addition of alkali metal cations, the fluorescence intensity of the polymers decreased sharply for Tl⁺ less for Cs⁺ and little for Li⁺, K⁺ and Rb⁺. On addition of alkaline earth metal cations, Ba²⁺ caused the strongest decrease of the fluorescence intensity of the polymers. The decrease of the fluorescence intensity of the polymers was suggested to be caused by the external heavy-atom effect of the cations bound to the cavity of the crowned naphthalene moiety. The content of the crowned naphthalene units in the polymers affected the cation-dependent fluorescence change. The fluorescence change of the polymers based on the cation complexation competition was also studied.     

Phytochrome-mediated Phototropism in Adiantum Protonemata II. Participation of Phytochrome Dark Reversion

A microbeam irradiation technique was used to analyze phytochrome-mediated phototropism of the protonema of the fern Adiantum capillus-veneris. One side of the sub-apical zone of a dark-adapted protonema was irradiated with a red-light (R) microbeam to induce phototropic curvature toward the irradiated side. Except the cases where fluence-response relationships were examined, the protonema was stimulated with the microbeam for about 30 s to provide a fluence (5.3–5.5 mmol m^-2) optimal for curvature. When the whole protonema was pretreated with a high fluence of R (about 9 mmol m^-2), no significant curvature could be induced by immediately subsequent one-sided microbeam stimulation. It was found, however, that curvature became inducible progressively as the time of microbeam stimulation was delayed after the R pretreatment. The protonema gained nearly full responsiveness within 40 min after the pretreatment. Moreover, the inductive effect of microbeam R escaped rapidly from the reversing effect of far-red light. These results indicated that most of the far-red-absorbing form of phytochrome (Pfr), which mediates the phototropic response, undergoes relatively fast dark reversion to the red-absorbing form. The dark reversion kinetics was analyzed further by taking into account that the phototropic responsiveness after the R pretreatment was measured in the presence of background Pfr over the protonema. This analysis revealed a rate constant of about 0.002 s^-1 (t_1/2? 6 min) for the dark reversion. It is considered that the Pfr dark reversion plays a role in establishing a lateral Pfr gradient in the unilaterally irradiated protonema.