Benzothiadiazole-based dyes that emit red light in solution,solid, and liquid state

In this paper, we report the preparation and red-light-emitting behavior of benzothiadiazole–tris(alkyloxy)phenylethene dyes. In solution, we observed an efficient red light emission with high fluorescence quantum yields (up to 0.78). With increase in solvent polarity, the emission bands shifted to longer wavelengths accompanied by a large Stokes shift of up to 152 nm. A moderate fluorescence quantum yield of 0.52 could be achieved even in the polar solvent dimethylformamide. Red light emission with good fluorescence quantum yields (up to 0.50) was also observed in the bulk solid, liquid, and film state.     

Preparation of Micron‐Sized Monodisperse Poly(ionic liquid) Particles

Micron‐sized monodisperse poly(ionic liquid) (PIL) particles, poly([2‐(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide), were prepared by dispersion polymerization at 70 °C in methanol with poly(vinylpyrrolidone) as a stabilizer. The obtained particle size could be controlled by addition of ethanol to the methanol medium while maintaining narrow monodispersity. The PIL particles exhibit unique properties; they can be observed by scanning electron microscopy without platinum coating, which is generally used to avoid an electron charge. Moreover, the solubility of the PIL particles can be easily changed by changing the counter anion, similar to the process for ionic liquids.     

M?ssbauer spectroscopic study on valence-detrapping and trapping of mixed-valence trinuclear iron(III, III, II) fluorine-substituted benzoate complexes

Magnetorheological (MR) fluids are new iron-based materials, whose applications include brakes, dampers, clutches, shock absorbers systems and polishing of optical surfaces (lens and mirrors). They are dependent on the size and shape of particles as the magnetic properties. Interested in the possibility of using iron-rich powders, commonly used in nondestructive testing, ranging in size from a few μm to about 200?μm and lower cost than those commercially used for MR fluids, a study of the structural and magnetic properties of iron-rich metallic particles by X-ray diffraction (XRD) and M?ssbauer spectroscopy (MS) at room temperature has been done. Powders, as received, were separated into particle sizes smaller than 20?μm (sample A) and in the range of 20–38?μm (sample B) because these are the sizes generally required for applications in MR fluids. The particles whose sizes exceed the above values were ground in a high energy planetary mill for 3?h, using different values of rotational speed/time: 200?rpm for one hour, a pause of 10?s, 140?rpm for one hour, pause 10?s and then 175?rpm during the last hour. These powders were sieved to obtain particles smaller than 20?μm (sample C). According XRD results, in all samples, only α-Fe (lattice parameter a = 2,867(2) ?) and Fe₂O₃ (lattice parameter a = 5,037(1) ? and c = 13,755(8) ?) were present. The M?ssbauer spectra were fitted with two sextets. The hyperfine parameters values allowed us to assign the highest relative area spectrum (sextet) corresponding to α-Fe and the second one to Fe₂O₃ in accord to the XRD results. Thus, the preparation method using mechanical milling for diminishing the size of the metallic particles allowed us to get particles with size and magnetic properties that could lead to potentially MR fluids applications.     

Wetting mode transition of nanoliter scale water droplets during evaporation on superhydrophobic surfaces with random roughness structure

During evaporation, shape changes of nanoliter-scale (80-100 nL) water droplets were evaluated on two superhydrophobic surfaces with different random roughness (nm-coating, μm-coating). The square of the contact radius and the square of the droplet height decreased linearly with evaporation time. However, trend changes were observed at around 170 s (nm-coating) and around 150 s (μm-coating) suggesting a wetting mode transition. The calculated droplet radii for the wetting mode transition from the average roughness distance and the average roughness height of these surface structures were approximately equal to the experimental values at these trend changes. A certain level of correlation between the roughness size and droplet radius at the wetting mode transition was confirmed on surfaces with random roughness.     

Preparation and Ferroelectric Properties of YMnO3 Thin Films with c-Axis Preferred Orientation by the Sol-Gel Method

Hexagonal YMnO₃ has a ferroelectric property with an optimal remanent polarization along the c-axis. The c-axis oriented YMnO₃ thin films with a small leakage current were prepared by the sol-gel dipping method. The c-axis orientation of the films was promoted by the addition of diethanolamine to the Mn precursor solution. A heat treatment with multiple steps led to a dense film structure with fine grains. The dense structure resulted in the decrease of the leakage current. Furthermore, when the films were heat-treated in a vacuum, the leakage current became considerably small and the ferroelectricity of the YMnO₃ thin films was observed even at room temperature.     

Enantioselective total synthesis of anti HIV-1 active (+)-calanolide A through a quinine-catalyzed asymmetric intramolecular oxo-Michael addition

Enantioselective total synthesis of anti HIV-1 active (+)-calanolide A was achieved by a quinine-catalyzed asymmetric intramolecular oxo-Michael addition as a key step.     

Production of core/shell polystyrene/poly(3,5-xylidine) composite particles by chemical oxidative seeded dispersion polymerization

Micron-sized monodispersed polystyrene (PS)/poly(3,5-xylidine) (PXy) composite particles were produced by chemical oxidative seeded dispersion polymerization of 3,5-xylidine at 20 °C with 1.6-μm-sized monodispersed PS seed particles in HCl aqueous solution, the pH of which was always kept at 2.5 with a pH stat. The composite particles produced consisted of a PS core and a PXy shell. Received: 16 December 1998 Accepted in revised form: 25 March 1999     

A first high enantiocontrol of an asymmetric tertiary carbon center attached with a fluoroalkyl group via Rh(I)-catalyzed conjugate addition reaction

Treatment of fluoroalkylated electron-deficient olefins with various boronic acids in the presence of a catalytic amount of Rh(I) coordinated with (S)-BINAP in toluene/H₂O at the reflux temperature for 3 h gave the corresponding conjugate addition products with high enantioselectivity in high yields.     

Synthesis of optically active methyl 4-(4-biphenylyl)-3-hydroxybutanoate via enantioselective hydrogenation using a tartaric acid-modified nickel catalyst and recrystallization

Enantioselective hydrogenation of methyl 4-(4-biphenylyl)-3-oxobutanoate over a tartaric acid-modified Raney nickel catalyst gave the title compound in 82% ee, which was enantiomerically enriched by recrystallizations. The product was converted to an (R)-3-acetoxyglutaric acid half ester via a ruthenium-catalyzed oxidation.