Electrical conducting and magnetic properties of (ethylenedithiotetrathiafulvalenothioquinone-1,3-diselenolemethide)2.FeBr4 (GaBr4) crystals with two different interlayer arrangements of donor molecules

Two donor molecules newly synthesized, dimethylthio- and ethylenedithio-tetrathiafulvalenothioquinone-1,3-diselenolemethides (1 and 2), were used to prepare their charge-transfer (CT) salts with a magnetic FeBr(4)(-) counteranion. For 1, a low electrical conducting 1:1 salt (1.FeBr(4)) was obtained, in which molecules of 1 are tightly dimerized in a one-dimensional (1D) stacking column. On the other hand, 2 gave a 2:1 salt (2(2).FeBr(4)) as two different kinds of plate crystals (I and II). Both I and II possess similar stacking structures of molecules of 2 in each 1D column with a half-cut pipelike structure along the c axis. However, for I, the stacking columns are aligned in the same direction along the a and b axes, while for II they are in the same direction along the a axis, but in the reverse direction along the b axis, resulting in the difference in the relative arrangement of molecules of 2 and FeBr(4)(-) ions between the two crystals. The room-temperature electrical conductivities of the single crystals of I and II were 13.6 and 12.7 S cm(-)(1), respectively. The electrical conducting behavior in I was metallic above 170 K but changed to be semiconducting with a very small activation energy of 7.0 meV in the temperature range 4-170 K. In contrast, II showed the semiconducting behavior in the whole temperature range 77-285 K. The corresponding nonmagnetic GaBr(4)(-) salts with almost the same crystal structure as I and II showed definitively different electrical conducting properties in the metal to semiconductor transition temperature in I as well as in the magnitude of activation energy in the semiconducting region of I and II. The interaction between the d spins of FeBr(4)(-) ions was weak and antiferromagnetic in both I and II, but the magnitude of the spin interaction was unexpectedly larger compared with that in the FeBr(4)(-) salt of the corresponding sulfur derivative of 2 with closer contact between the neighboring FeBr(4)(-) ions. These electrical conducting and magnetic results suggest a significant interaction between the conducting pi electrons and the d spins of FeBr(4)(-) ions located near the columns or layers.     

Antitumor activity of Hypsizigus marmoreus. I. Antitumor activity of extracts and polysaccharides.

Antitumor activity of Hypsizigus marmoreus, one of the most popular Japanese edible mushrooms, was investigated. The aqueous and methanol extracts were tested against allogeneic tumor, solid sarcoma 180 and syngeneic tumor, Meth A fibrosarcoma. The aqueous extract was highly active in inhibiting growth of solid sarcoma 180, but not as much for Meth A fibrosarcoma. Fractionation of antitumor substances of the aqueous extract isolated four polysaccharides. Chemical analysis revealed one of them to be beta-(1-3)-glucan with a remarkable inhibitory effect against tumor-growth of sarcoma 180.     

Optically active 1,2-bis(1-arylhydroxymethyl) ferrocene: a new, efficient chiral ligand for scandium-catalyzed asymmetric Diels-Alder reaction

[reaction: see text] The Sc(OTf)3/FERRODIOL (2) complex was prepared at -78 degrees C in CH2Cl2 in the presence of 2,6-lutidine and MS 4A. The chiral scandium Lewis acid-catalyzed asymmetric Diels-Alder reaction of cyclopentadiene (3) with 3-acyloxazolidin-2-ones (4) effectively produced the adduct (5) in a high yield with good selectivity, i.e., endo/exo = 90:10 up to 91% ee (endo).     

Effect of syndiotacticity on the aqueous poly(vinyl alcohol) gel 3. Mechanical property of gel

Summary The mechanical property of aqueous gel was studied using the PVA having the content of syndiotacticity in diad from 58.4 and 66.2%. The elastic modulus of gels was 105–106 dyne/cm2 and the variation of the elastic modulus of gel with the rise of temperature was corresponded with the variation of the concentration of PVA in gel accompanying syneresis. The elastic modulus of gel having the same content of syndiotacticity and concentration of PVA increased in the order as follows, the first is the gel chilled at room temperature, the second is the gel chilled at 60 °C and last is the gel chilled at 0 °C. The variation of the elastic modulus of gel with the rise of temperature became smaller with increasing content of syndiotacticity. The increase of elastic modulus is considered to be attributed to the further growth of stronger junctions through the recrystallization followed by syneresis rather than the entropic effect of polymer networks with the rise of temperature.

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Zusammenfassung Es wurden die mechanischen Eigenschaften wßriger Gele aus Polyvinylalkohol untersucht, mit Gehalten an Syndioaktizität in Diaden zwischen 58,4 und 66,2%. Die elastischen Moduln der Gele lagen bei 105 bis 106 dyn/cm2 und die Variation der elastischen Moduln der Gele mit Steigerung der Temperatur entsprach der Konzentrationsänderung von Polyvinylalkohol im Gele gemäß der stattgefundenen Synärese. Der elastische Modul des Gels mit konstantem Gehalt an Syndiotaktizität und Konzentration des PVA steigen in folgender Weise: Zuerst das Gel abgekühlt bei Raumtemperatur, dann das Gel abgekühlt bei 60 °C und zuletzt das Gel erstarrt bei 0 °C. Die Variation der elastischen Moduln mit steigender Temperatur wird kleiner mit steigendem Gehalt an Syndiotaktizität. Das Anwachsen der Moduln sollte vermutlich dem weiteren Wachstum strengerer Kopp lungen durch Rekristallisation infolge der Synärese zuzuschreiben sein mehr als einem Entropieeffekt der polymeren Netzwerke mit steigender Temperatur.

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With 6 figures and 2 tables

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Part 2. cf. reference 2.     

Double tracer whole body autoradiography using a short-lived positron emitter and a long-lived beta emitter

We investigated glucose and amino acid metabolism in tumors and other organs using whole body autoradiography with a short-lived positron emitter and a long-lived beta emitter. The radioactive compounds used were 2-deoxy-2-[18F]-fluoro-D-glucose (18F-FDG) with a half life of 109.8 min and L-[methyl-14C]-methionine (14C-MET) with a half life of 5,730 years. A Donryu rat weighing about 150 g was subcutaneously inoculated at the back with experimental tumors of AH109A and AH272. 74 MBq (2 mCi) of 18F-FDG and 740 kBq (20 microCi) of 14C-MET was administered and after 30 min, the rat was sacrificed. Whole body frozen sections were obtained using autocryotome. For the 18F-FDG autoradiogram, the frozen sections were exposed to an X-ray film for 6 h. After seven days, these frozen sections were again exposed to 14C-MET for a week. Cross-contamination was minimized by adjusting the exposure time, the interval of exposures and the administered dose. The accumulation of the tracers was represented as the optical density ratio of the tissue of interest to the muscle. The tumor ratios were 12.5 for 18F-FDG and 8.6 for 14C-MET showing the highest accumulation in the whole body autoradiogram. In contrast the inflammatory tissue ratios were 1.27 for 18F-FDG and 0.77 for 14C-MET showing very low amino acid metabolism. With the present double tracer whole body autoradiogram, 18F-FDG accumulation was seen in the brain and the heart but not to the liver as against 14C-MET accumulation which was seen to the liver but not to the brain and the heart.     

Comparative studies on 99mTc-pyrophosphate and 85Sr-chloride for skeletal imaging

In order to know the potential merits of 99mTc-pyrophosphate (99mTc-PYP) skeletal imaging, a comparative study was carried out by administering to the rabbit 85Sr-chloride (85Sr), classical bone-seeking agent, and 99mTc-PY simultaneously. Radioisotopic distribution was investigated as regards their deposition in the pelvic bones, and sharpness of the skeletal scintigrams, too. Both agents were remarkably affinitive to the skeletal system and there were remarkably differences in their temporal deposition pattern. Marked deposition was observed of either agent in the metaphyses. With 99mTc-PYP, the vertebral and costal systems were delineated symmetrically and each vertebral body was distinctly depicted as such 99mTc-PYP many possess the following merits over 85Sr; (1) owing to its physical properties, sufficiently large radioactivity of 99mTc-can be administered; (2) body burden of radiation absorption is reduced; (3) skeletal scintigrams of high quality are obtainable in a short period of time.     

Polycyclic N-hetero compounds. XXXIV. Syntheses and evaluation of antidepressive activity of benzofuro-[2,3-e]imidazo[1,2-c]pyrimidines and their precursors

Syntheses of 2,3-dihydrobenzofuro[2,3-e]imidazo[1,2-c]pyrimidine and its 5-substituted derivatives, corresponding to B-nor-6-oxa-11,13,15-triazasteroids, are described. These products and their precursors were screened to evaluate the antidepressive activity.     

Synthesis and structure of 16 pi octaalkyltetraphenylporphyrins

The oxidized octaethyltetraphenylporphyrin (1, OETPP) and the corresponding newly prepared octaisobutyltetraphenylporphyrin (3, OisoBuTPP) could be isolated from the reaction of OETPPLi2 (or OisoBuTPPLi2) with SOCl2. The X-ray analysis and the characteristic UV-vis spectra of 1 and 3 revealed that these are the first examples of 16 pi nonaromatic porphyrins.     

Photocrosslinkable polyesters with conjugated double bonds: Reciprocity effect in laser recording

The reciprocity effect under intense illumination was studied with photocrosslinkable polyesters of p-phenylenebis(α-cyanobutadiene carboxylic acid) (I), m-phenylenebis(α-cyanobutadiene carboxylic acid) (II), and p-phenylenebis(acrylic acid) (III), with an argon ion laser as a light source. The reciprocal sensitivities of I, II, and III were 5.0, 1800, and > 10⁵ mJ/cm², respectively. II and III required sensitization to enhance their sensitivities to a level at which reciprocity effects could be measured. I obeyed the reciprocity law over a wide range of exposure times from seconds to microseconds. Both II′, a copolyester of II, and III showed a dramatic decrease of sensitivity in high-intensity/short-time exposure when sensitized by 9,10-phenanthraquinone and pyrylium salts.     

Time-dependent density functional theory calculations of the photoabsorption of fluorinated alkanes

Time-dependent density functional theory (TD-DFT) calculations of the transition energies and oscillator strengths of fluorinated alkanes have been performed. The TD-DFT method with the non-local B3LYP potential yields transition energies for the methanes, which are smaller by about 10% as compared to the experimental values. An empirical linear correlation was found between the calculated and experimental transition energies both at the B3LYP/DZ+Ryd(C, F) and B3LYP/cc-pVTZ+Ryd(C, F, H) levels for a total of 19 transitions of the fluorinated methanes with linear correlation coefficients of 0.987 for the former and 0.988 for the latter. This empirical correlation for fluorinated methane molecules is found to agree well with the previously obtained empirical correlations between calculated and experimental values for non-fluorinated molecules. The results show that a single empirical-correlation relationship can be used for both non-fluorinated and fluorinated molecules to predict transition energies. This linear relationship is then used to predict the photoabsorption spectra of ethane, propane, butane, and partially and fully fluorinated derivatives. A key result of these calculations is the dominance of Rydberg transitions in the spectral region of interest.