Electron-phonon interactions in the monocations of polyacetylenes

Electron-phonon interactions in the monocations of trans-polyacetylenes such as C2H4 (2tpa), C4H6 (2tpa), C6H8 (6tpa), and C8H10 (8tpa) are studied. The C-C stretching Ag modes around 1700 cm(-1) afford the largest electron-phonon coupling constants in the monocations of polyacetylenes. However, the C-C bending Ag modes around 1200 cm(-1) afford much smaller electron-phonon coupling constants than the C-C stretching Ag modes around 1700 cm(-1) in the monocations of polyacetylenes. The total electron-phonon coupling constants for the monocations (l HOMO) are estimated to be 0.357, 0.285, 0.281, and 0.279 eV for 2tpa, 4tpa, 6tpa, and 8tpa, respectively. The l HOMO values for polyacetylenes with C 2h geometry hardly change with an increase in molecular size while those for polyacenes with D 2h geometry significantly decrease with an increase in molecular size. The l HOMO values for polyacetylenes are larger than those for polyacenes. The calculated results are rationalized in terms of the phase patterns of the molecular orbitals in detail. The electron transfer in the positively charged polyacetylenes is also discussed. Intramolecular electron mobility (sigma(intra,monocation)) in the positively charged polyacetylenes is estimated to be smaller than those for the positively charged polyacenes. The reorganization energies for the positively charged polyacetylenes are estimated to be larger than those for the positively charged polyacenes. Thus, the larger overlap integrals between two neighboring molecules are needed for the positively charged polyacetylenes to become good conductor than those for positively charged polyacenes. On the other hand, the conditions under which the electron-electron interactions are attractive are more easily realized in the monocations of polyacetylenes than in the monocations of polyacenes. The quality as conducting materials would not significantly depend on the molecular size in the positively charged polyacetylenes, compared with that in the positively charged polyacenes. Multimode problem is also treated in order to investigate how consideration of multimode problem is closely related to the characteristics of the electron-phonon interactions.     

Photophysical properties and photocatalytic activities of bismuth molybdates under visible light irradiation

Aurivillius structure Bi(2)MoO(6) (BG: 2.70 eV) that is a low-temperature phase showed an intense absorption band in the visible light region and photocatalytic activity for O(2) evolution from an aqueous silver nitrate solution under visible light irradiation, among various bismuth molybdates (Bi(2)MoO(6), Bi(2)Mo(2)O(9), and Bi(2)Mo(3)O(12)) synthesized by solid-state and reflux reactions. Bi(2)Mo(3)O(12) (BG: 2.88 eV) also showed photocatalytic activity for O(2) evolution under full-arc irradiation of a Xe lamp (lambda > 300 nm). The photocatalytic activity of the Aurivillius structure Bi(2)MoO(6) prepared by the reflux method was dependent on the annealing temperature after the preparation. The crystallinity was the important factor for the activity. Calculation by the density functional method indicated that the conduction band of Aurivillius structure Bi(2)MoO(6) was made up of Mo 4d orbitals. It turned out that the visible-light absorption of this photocatalyst was due to the transition from the valence band consisting of O 2p orbitals to the conduction band. The corner-sharing structure of the MoO(6) octahedra contributed to the visible light response and the photocatalytic performance because excitation energy and/or photogenerated electron and hole pairs began to migrate easily in the Aurivillius structure.     

Palladium-catalyzed regiocontrolled alpha-arylation of trimethylsilyl enol ethers with aryl halides

Inter- and intramolecular arylations of trimethylsilyl enol ethers with aryl halides are accomplished regiospecifically in the presence of a palladium catalyst and tributyltin fluoride in refluxing benzene or toluene. The optimal catalyst system called for the use of Pd2(dba)3 and tri-tert-butylphosphine in ca. 1:2 ratio. Aryl iodides, bromides, and chlorides are all effective arylation partners in this reaction. [reaction: see text]     

Creation of superior carboxyfluorescein dyes by blocking donor-excited photoinduced electron transfer

[Structure: see text] Carboxyfluoresceins are widely utilized as fluorescence labeling reagents, but we recently found that their emission intensity is markedly decreased after esterification. On the basis of our hypothesis that the fluorescence decrease is due to a donor-excited photoinduced electron transfer (d-PeT) process, we have developed novel carboxyfluorescein derivatives in which the d-PeT process is hampered, and the emission intensity is not decreased upon esterification. These novel dye derivatives display high quantum yields and are expected to be useful as labeling agents.     

Simultaneous analysis of cationic, anionic, and neutral compounds using monolithic CEC columns

A new capillary electrochromatography (CEC) column for the simultaneous analysis of cationic, neutral, and anionic compounds using CEC-ESI-MS is described. Three different silica monolith columns were prepared by changing the poly(ethylene glycol) (PEG) contents for comparison of the separation property of these columns. Different separation programs were used for the simultaneous separation of different charged compounds under the same conditions. The column prepared with 80 mg of PEG separated typical compounds within 15 min using 1 M formic acid as the electrolyte. The analytes migrated in the order of cationic, neutral, and anionic compounds, which means that the migration order was mainly determined by the electrophoresis. The hydrodynamic flow by pressure from the inlet side was significant for a stable analysis to be achieved. The effect of the composition of the sheath liquid was also examined. All analytes (14 amino acids, thiourea, urea, citric acid, and ATP) were detectable when 1% acetic acid in 50% (v/v) methanol was used as the sheath liquid.     

Electron conductive three-dimensional polymer of cuboidal C60

Single crystals of three-dimensional (3D) C60 polymer were prepared by the topotactic conversion of two-dimensional (2D) C60 polymer single crystals at a pressure of 15 GPa at 600 degrees C. The x-ray single crystal study revealed that the 3D C60 polymer crystallized in a body centered orthorhombic space group Immm, and spherical C60 monomer units were substantially deformed to rectangular parallelepiped (cuboidal) shapes, each unit being bonded to eight cuboidal C60 neighbors via [3 + 3] cycloaddition. The 3D C60 polymer was electron conductive, in contrast with the nonconductive behavior of 2D polymers.     

Terahertz surface-wave resonant sensor with a metal hole array

A surface-wave sensor based on the resonant transmission characteristics of metal hole arrays is demonstrated in the terahertz (THz) region. Since the frequency of the transmission peak of a metal hole array, which corresponds to the resonant frequency of the surface waves, is particularly sensitive to the refractive index in the vicinity of the metal surface, a very small change in the substances attached to the surface can be detected by monitoring the transmission spectrum. By attaching a layer of substance (thickness t < 5 microm) much thinner than the wavelength of the THz wave (lambda(THz) = 1 mm at 0.3 THz) to the surface of a metal hole array, we demonstrated that the existence of such a small amount of substance can be detected more easily than without the metal hole array. This demonstration of THz sensing with metal hole arrays indicates the possibility of realizing THz surface-wave sensors for biochemical molecules in the THz region.     

Parabolic Martin Boundaries and Asymptotic Formulas of Heat Kernels for One-Dimensional Elliptic Operators with Periodic Coefficients

We determine the Martin boundary of R × (???∞?, 0) for operators \(\partial_t+L\), where L is a one-dimensional second-order elliptic operator with periodic coefficients. We also give long-time asymptotic formulas of heat kernels generated by L in the case that the ratio of the spatial variable to the time variable is large or small.     

Assessment of the natural radioactivity using two techniques for the measurement of radionuclide concentration in building materials used in Japan

The specific activities of ²³⁸U, ²³²Th, and ⁴⁰K in selected building materials used in Japan were measured using a high-purity germanium detector. The uranium and thorium concentrations were determined from same samples using inductively coupled plasma mass spectrometry. There was a good agreement between the measurement of uranium and thorium with both methods (R ² = 0.94, and 0.97, respectively). Based on the specific activities, we have estimated some hazard indexes such as radium equivalent activities (Ra _eq), external hazard index (H _ex), internal hazard index (H _in), annual gonadal equivalent dose (AGED), internal alpha dose, mass exhalation rate and emanation coefficient of radon.     

Synthesis and spectroscopic study of phenylene-(poly)ethynylenes substituted by amino or amino/cyano groups at terminal(s): electronic effect of cyano group on charge-transfer excitation of acetylenic π-systems

To gain insight into substituent electronic effect on charge-transfer excitation of acetylenic π-systems, phenylene-(poly)ethynylenes substituted by Ph₂N or Ph₂N/cyano groups were synthesized by combination of Sonogashira coupling and double elimination protocol of β-substituted sulfones. These substituted phenyleneethynylenes showed large molar absorption coefficients ?, and emitted strong fluorescence upon UV light irradiation. Phenylene-(poly)ethynylenes, which involve butadiyne or hexatriyne motifs, emitted fluorescence in remarkably lower fluorescence quantum yields Φ_F as their polyethynylene motifs -(CC)_n- expanded. The drastic decrease of fluorescence quantum yields Φ_F were explained in terms of increasing nonradiative reaction rate constants k_nr, which had been determined by the corresponding fluorescence quantum yields Φ_F and lifetime values τ. The emission underwent a large bathochromic shift in polar solvents because the charge-separated excited state is more stabilized than the ground state. Comparison of slope values ρ in Lippert/Mataga plot for the Ph₂N and Ph₂N/cyano-substituted phenylene-(poly)ethynylenes revealed that the latter underwent large change of dipole moments upon photo-excitation although highly expanded acetylenic π-systems with cyano group did little.