Exafs study of FeCl3-doped polyacetylene

FeK absorption spectra of FeCl₃-doped polyacetylene [CH(FeCl₃)_y]_x having y values of 0.024, 0.087 and 0.13, were measured by use of synchrotron radiation. The analyses of observed EXAFS data showed that Fe atom is surrounded by about four Cl atoms with Fe-Cl distance of 2.18–2.20 Å. It is concluded that the dopant exists mainly in the form of FeCl₄^-, and the following reaction takes place in the FeCl₃ doping process. 2FeCl₃ + e^- → FeCl₄^- + FeCl₂     

Production of heavy resonances with electron and muon beams

The inelastic leptoproduction of heavy resonances J (J = J/ψ, Ψ,…) is investigated in a model where γ_vg → Jg is assumed to be the dominant mechanism. Analytic expressions for the differential cross section as well as for the helicity amplitudes are presented. A detailed numerical analysis of the angular distribution of the muon pair arising from the decay of the heavy resonance in its rest frame is presented.     

Plutonium-244 dating VI. Initial ratios of plutonium to uranium in achondrites

Re-examination of all known xenon isotopic data for achondrites reveals that²⁴⁴Pu fission xenon can be resolved in about three-fourths of the meteorites of this class. The amounts of²⁴⁴Pu fission xenon found in these meteorites range from ca. 1–2 up to 20–40·10^–12 ccSTP/g. These meteorites started to retain their xenon some 200–500 million years later than did the carbonaceous chondrites Allende, Groznaya, Mokoia, Murchison, Murray, and Renazzo, which began to retain their xenon over 4800 million years ago.     

Spin-polarized Dirac-cone-like surface state with d character at W(110)

The surface of W(110) exhibits a Dirac-cone-like state with d character within a spin-orbit-induced symmetry gap. As a function of the wave vector parallel to the surface, it shows a nearly massless energy dispersion and a pronounced spin polarization, which is antisymmetric with respect to the Brillouin zone center. In addition, the observed constant energy contours are strongly anisotropic for all energies. This discovery opens new pathways to the study of surface spin-density waves arising from a strong Fermi surface nesting as well as d-electron-based topological properties.     

Di-isotacticity of poly(methyl propenyl ether) and double-bond opening of methyl propenyl ether in cationic polymerization

The di-isotacticity of poly(methylpropenyl ether) obtained by the cationic polymerization has been studied by NMR spectra. The NMR spectra of β-methyl protons of the polymer are decoupled from the β-methine proton spectra to determine the di-isotactic fraction in a polymer. The signals of β-methyl protons at 8.78 and 8.89 τ are estimated as spectra based on threo- and erythro-di-isotactic diads, respectively. With BF₃·O(C₂H₅)₂ as a catalyst, the trans monomer yields a crystalline polymer and its structure is threo-di-isotactic. Otherwise, cis monomer produces an amorphous polymer, and it is a mixture of threo- and erythro-di-isotactic structure. From these results, it is concluded that the double bond in trans monomer is opened exclusively in the cis type, and in cis monomer cis- and trans-openings take place at almost the same rate.     

Development of hydrophilic fluorogenic derivatization reagents for thiols: 4-(N-acetylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole and 4-(N-trichloroacetylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole

Sensitive, reactive, and hydrophilic fluorogenic reagents for thiols with the benzofurazan skeleton, 4-(N-acetylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole (AcABD-F) and 4-(N-trichloroacetylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole (TCAcABD-F) have been developed. These reagents reacted with thiols within 10 min at 60 degrees C. AcABD-F and TCAcABD-F themselves do not fluoresce but are strongly fluorescent after the reaction with thiol compounds. The generated derivatives were highly water-soluble, since they dissociated a proton and ionized in the neutral pH region. The derivatives with four biologically important thiol compounds were separated on a reversed-phase HPLC column and detected fluorometrically at 504 nm with excitation at 388 nm. The detection limit attained for homocysteine with AcABD-F was 25 fmol on column (11 nM) (signal-to-noise ratio = 3), and that for glutathione with TCAcABD-F was 45 fmol on column (20 nM).