Metallic conductivity and ferromagnetic interaction of iron(III) d spins in the needle crystals of (ethylenedithiotetrathiafulvalenoquinone-1,3-dithiolemethide)(2).FeBr(4) salt

The 2:1 charge-transfer (CT) salts (1(2).FeBr(4) and 1(2).GaBr(4)) of ethylenedithiotetrathiafulvalenoquinone-1,3-dithiolemethide (1) with FeBr(4)(-) and GaBr(4)(-) counteranions were obtained as needle crystals, whose structures are almost the same as each other. The 1 molecules form a one dimensionally stacked column with alternation of their molecular axis direction, while the counteranions are aligned in parallel with the 1-stacked columns with the direction of their distorted-tetrahedral geometry maintained. The room-temperature electrical conductivities measured on the single crystals of 1(2).FeBr(4) and 1(2).GaBr(4) were 4.6 and 2.1 S cm(-1), respectively. From the temperature dependences of their electrical conductivities in both cases the electrical conducting properties were metallic between ca. 170 and 300 K, but below ca. 170 K converted to be semiconducting and continued till 5 K, although the activation energies are very small (4-10 meV). For 1(2).FeBr(4) very weak and antiferromagnetic interaction occurred between the d spins of FeBr(4)(-) ions in the temperature range of ca. 1-300 K. However, below ca. 15 K the ferromagnetic interaction was reversely preferential possibly by participation of the pi spin of 1.     

Controlled monomer insertion into polymer main chain: synthesis of sequence ordered polystyrene containing thiourethane and trithiocarbonate units by the RAFT process

A polymer having a trithiocarbonate moiety in the main chain was applied as a polymeric precursor to the synthesis of a sequence ordered polymer by insertion polymerization of styrene into the main chain by a RAFT mechanism.     

Total synthesis of ecteinascidin 743

The total synthesis of ecteinascidin 743 (1), an extremely potent antitumor agent, has been accomplished. The synthesis features Ugi's 4CC reaction, intramolecular Heck reaction, phenol-aldehyde cyclization, and acid-induced intramolecular sulfide formation.     

Relationship between apparent diffusion coefficient and signal intensity in endometrial and other pelvic cysts

We evaluated whether apparent diffusion coefficient (ADC) value is more useful than signal intensity for differentiating endometrial cysts from other pelvic cysts. In an in vitro study, signal intensity and diffusion coefficients were measured in whole blood phantoms in which blood oxidation was gradually increased and concentration subsequently diluted. Although both signal intensity and diffusion value were largely affected by blood concentration, diffusion value was almost independent of blood oxidation and red blood cell lysis-related diminution of magnetic nonhomogeneity, both factors greatly affecting signal intensity on T1- and T2-weighted images. In an in vivo study, differentiation between endometrial and other pelvic cysts was attempted by means of ADC values and signal ratios of cysts to muscles on T1- and T2-weighted images (T1- and T2-ratios). Endometrial cysts tended to show lower T2-ratios, higher T1-ratios, and lower ADC values than other pelvic cysts (p < 0.001). However, ADC values were not correlated with T1- and T2-ratios (p < /0.15/). The ability of ADC value to discriminate between these two groups (discriminant rate, 91.4%) was higher than that of T2-ratio (71.4%) or T1-ratio (88.6%). If combined, ADC and T1-ratio (or T2-ratio) showed higher discriminant rate (94.3%) than the combination of T1- and T2 ratios (88.6%). ADC value might be useful for evaluating the blood concentration of a cystic lesion, because diffusion value is more closely related to blood concentration and almost independent of blood oxidation and red blood cell lysis that largely affect signal intensity.     

Normal stress and shear stress in a viscoelastic liquid under steady shear flow: Effect of molecular weight heterogeneity

Under steady shear flow, the normal stress and the shear stress in both dilute and concentrated solutions of monodisperse poly-α-methylstyrenes and their blends were measured. It was confirmed that the molecular theories of Rouse and Zimm extended to concentrated solutions can explain the relation between the zero-shear normal stress coefficient and the zero-shear steady-flow viscosity for both monodisperse and polydisperse systems. Shear-rate dependence of steady-flow viscosity can be understood fairly well by the molecular entanglement concept proposed by Graessley so long as the polymer is monodisperse or the amount of the higher molecular weight component is high. However, zero-shear viscosity of blended systems cannot be explained quantitatively by the theory of Graessley. The shear-rate dependence of steady-state compliance of blended systems was also observed, and it can well be explained by the theory of Tanaka, Yamamoto, and Takano which interpreted the shear rate-dependent steady-state compliance in terms of the relaxation time spectrum and its variation with shear rate.     

Surface properties of styrene–ethylene oxide block copolymers

Hydrophobic–hydrophilic block copolymers were prepared by “living” anionic polymerization. They consist of polystyrene and poly(ethylene oxide) blocks, and are soluble in water. Their interfacial properties were investigated, employing aqueous solutions. The block copolymers lowered the surface tension of water in analogy with the low molecular weight surfactants such as sodium lauryl sulfate and heptaethylene oxide n-dodecyl ether. Their aqueous solutions exhibited solubilization properties differing from those of polyethylene glycol. Therefore, it is thought that the polystyrene blocks produce solubilization phenomena. In samples of the same styrene content, the precipitation temperature of a high molecular weight copolymer in water was lower than that of a low molecular weight copolymer at the same concentration in the same solvent. The surface tension and precipitation temperature of aqueous solutions seem to be influenced by molecular weight and composition.     

On the miscibility gap in liquid bismuth-bismuth tribromide system

We have determined the location of the miscibility gap in liquid Bi-BiBr₃ system in the concentration-temperature, x?T, plane from the measurement of the electrical conductivity. The measurements have been done in the concentration range between 30.5 and 92.5 mol.% Bi and in the temperature range between 300 and 600°C. It is found that the temperature dependence of the conductivity of the mixture changes near the retrograde solubility region.     

The phase boundary between α′- and tetragonal Ce

The phase boundary between the α'- and tetragonal high-pressure polymorphs of cerium was determined from the resistance anomaly. The phase boundary has a negative slope, ∂T/∂P = -7.56°C/kbar and appears to intersect the fusion curve in the neighborhood of the broad minimum.     

Studies of phase characteristics of various photon echoes with a phase sensitive detection method

Various optical coherent transient signals in ruby have been examined by using an optical phase sensitive detection (PSD) technique. The PSD is performed by comparing the phase of the heterodyne beat signals obtained by the Stark switching technique with that of a local oscillator whose frequency is equal to the heterodyne beat frequency. The optical FID, two-pulse photon echoes, radiation locked echoes and notched echoes have been detected as υ-mode signals with small u-mode signals probably due to the asymmetry of the inhomogeneous broadening. The dependence of the phase of the radiation locked and notched echoes upon the driving pulses is also examined. The experimental results are in good agreement with theoretical predictions based on Bloch equations.     

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.