Water-supported organized structures based on wedge-shaped amphiphilic derivatives of dipyrrolyldiketone boron complexes

Wedge-shaped amphiphilic derivatives of 1,3-dipyrrolyl-1,3-propanedione boron complexes, with one or no aliphatic chains attached at one aryl moiety and three hydrophilic chains at the other, exhibited formation of assembled structures in aqueous solutions. UV/vis, fluorescence and DLS analyses suggested that the wedge-shaped amphiphiles exist in assembled modes in the solution state, and TEM measurements revealed that a balance of hydrophobic and hydrophilic moieties in the amphiphiles is crucial for the formation of organized structures in aqueous solutions as evidenced by the formation of spherical and cylindrical micelles.     

AgSbF6-promoted cycloaddition reaction of 2-trifluoromethyl-N-tosylaziridine with aldehydes

2-Trifluoromethyl-N-tosylaziridine reacted with various aldehydes in the presence of a catalytic amount of AgSbF(6) to provide the corresponding cis-4-trifluoromethyl-2-substituted-N-tosyl-1,3-oxazolidines with excellent regio- and stereoselectivity.     

Discrepancy of Cross Sections in pd Breakup Reactions at E p = 250?MeV

In our previous inclusive experiment on ²H(p, p)pn at 247?MeV, the measured cross section at forward angles is about twice larger than 3N calculation with ?Ц? 3NF. Therefore, we have made an exclusive experiment on ²H(p, p ₁ p ₂)n at the same energy. The preliminary data suggest that the cross section was enhanced at forward angle of ?? ₁ and ?? ₂.     

Formation and Geometrical Control of Polygon‐Like Metal‐Coordination Assemblies

Polygon‐like [2+2]‐ and [3+3]‐type metal complexes were prepared from dipyrrin dimers connected by acute‐angled spacers. The electrical conduction depends strongly on the packing alignment of the compounds, revealing the presence of effective hopping pathways for holes with relatively high mobility up to 0.11 cm² V^?1 s^?1 along the aligned axis of [3+3]‐type metal‐bridged assemblies. These observations correlated with the geometrical control of the π‐conjugated metal complexes in the cyclic structures, which enables their ordered arrangement in the assemblies.     

Emission and transient absorption measurements of substitution effects of C–C triple bonds on relaxation processes of the fluorescent state of naphthalenes

Photophysical and photochemical properties of naphthalenes substituted with trimethylsilylethynyl, tert-butylethynyl, and trimethylsilylbutadiynyl groups were investigated by measurement of fluorescence yields, lifetimes, and triplet absorption. Introducing trimethylsilylethynyl and tert-butylethynyl groups to the 1-position of the naphthalene skeleton substantially enhanced fluorescence and intersystem crossing (ISC). The rates of fluorescence of 2-substituted naphthalenes were low. The effect of ethynyl groups on the 1-substituted naphthalenes was rationalized in terms of an increase of the transition moment along the short axis of the naphthalene skeleton. Substitution of the trimethylsilylbutadiynyl group at the 1 or 2-position of the naphthalene skeleton caused a considerable decrease in the fluorescence yield (approximately 0.01) and an increase in the ISC yield (0.99).     

Submillimeter-Wave Spectroscopy of TiCl in the Ground Electronic State

The submillimeter-wave rotational transitions of TiCl in the ground state were observed using a double-modulation technique. TiCl was generated in a DC-discharge of a mixture of TiCl₄ vapor (less than 1 mTorr) and Ar buffer gas (80 mTorr) at a current of 200 mA. The ⁴Φ_3/2, ⁴Φ_5/2, ⁴Φ_7/2, and ⁴Φ_9/2 spin components of Ti³⁵Cl (v=0, 1, 2) and Ti³⁷Cl (v=0) were detected. The data were analyzed using effective rotational constants for each spin component as well as with the usual N² reduced Hamiltonian. Recent Fourier transform and laser data were included in our fits and we confirm that the ground state of TiCl is a ⁴Φ_r electronic state.     

Monte Carlo simulation of spectral reflectance using a multilayered skin tissue model

A nine-layered skin tissue model is newly developed for the Monte Carlo simulation of spectral reflectance. The derivation of the necessary parameters for each of the nine layers in the simulation is presented, in which the parameters used in the conventional three-layered model are modified on the basis of some histological findings on skin and reported examples. Using appropriate optical and geometrical parameters, simulated spectra can be produced that agree well with measured spectra. This approach provides a flexible means of spectral fitting to measured results and of estimating changes in the parameters of skin tissue.     

Multiplicity dependence of the pion source in S+A collisions at the CERN SPS

The emission of pions from relativistic heavy-ion collisions of S+S, S+Ag and S+Pb at 200 GeV/nucleon is characterized using two-particle interferometry. The multiplicity dependence of the pion source parameters near midrapidity is studied. The transversal (R _t) and longitudinal (R _l) pion source parameters are independent of the initial nuclei in the interaction and increase with increasing multiplicity. This suggests that the freeze-out process is governed mainly by the particle multiplicity. The multiplicity dependence is weaker than that expected from a simple model of a freeze-out at a constant density.