Silver-catalyzed regioselective carbomagnesiation of alkynes with alkyl halides and Grignard reagents

A silver-catalyzed carbomagnesiation of alkynes with alkyl halides and Grignard reagents afforded alkenyl Grignard reagents regioselectively, where the alkyl group of the alkyl halide, but not that of the Grignard reagent, was introduced into the alkyne. Application to δ-haloalkylacetylenes yielded cyclopentanes or a tetrahydrofuran containing an exo-methylene substituent via 5-exo-dig cyclization.     

Numerical finite-difference time-domain calculation for extreme enhancement of magneto-optical effect at ultraviolet wavelength using Ni-subwavelength grating on SiO2/Ni structure

Optical Review - An extreme enhancement of the polar Kerr magneto-optical (MO) effect was numerically demonstrated using surface plasmon polaritons (SPPs) at the SiO2/Ni interface combined with the...     

Preparation of gold-, gold/silver-dendrimer nanocomposites in the presence of benzoin in ethanol by UV irradiation

Gold- and gold/silver-dendrimer nanocomposites have been synthesized by UV irradiation of their salts dissolved in ethanol containing dendrimers. As dendrimers, poly(amidomaine) PAMAM dendrimers and poly(propyleneimine) PPI dendrimers of various generations were used. The photoreduction of their salts is greatly accelerated by using benzoin as a photoinitiator. The sizes of gold in the nanocomposites are affected by the concentration of benzoin as well as the concentration of dendrimers, but are hardly changed with the kind of dendrimers. For gold/silver-dendrimer nanocomposites, the absorption spectra of gold/silver nanoparticles in the nanocomposites are very similar to the theoretical spectra of gold/silver alloy nanoparticles, suggesting the formation of gold/silver alloy nanoparticles. From the comparison of TEM and DLS measurements, it is found that the metal-dendrimer nanocomposites consist of metal nanoparticles covering by dendrimer molecules.     

Effect of thickness on the stability of transparent conducting impurity‐doped ZnO thin films in a high humidity environment

The resistivity of transparent conducting Al‐ and Ga‐doped ZnO (AZO and GZO) thin films prepared with a thickness in the range from 20 to 200 nm on glass substrates at a temperature below 200 °C was found to increase with exposure time when tested in a high humidity environment (air at 90% relative humidity and 60 °C). The resistivity stability (resistivity increase) was considerably affected by the thin film thickness. In particular, thin films with a thickness below about 50 nm were very unstable. The increase in resistivity is interpreted as carrier transport being dominated by grain boundary scattering resulting from the trapping of free electrons due to oxygen adsorption on the grain boundary surface. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Stereoselective pinacol coupling of chiral formylferrocene using divalent samarium triflate: preparation of a new chiral bisferrocenyl oxazoline ligand and its application to asymmetric Diels-Alder reactions

[reaction: see text] The pinacol coupling reaction of planar chiral ortho-oxazoline-substituted formylferrocene was smoothly mediated by SmI2 or Sm(OTf)3 to give the (R,R) isomer selectivity (up to 76% diastereomeric excess). The combination of Yb(OTf)3 and the (R,R)-ferrocenyl diol was revealed to be a good catalyst for the asymmetric Diels-Alder reaction of 3-acyloxazolidinone with cyclopentadiene, and the endo adduct was produced in up to 80% enantiomeric excess.     

Tandem ene-reaction/hydroamination of amino-olefin and -allene compounds catalyzed by Bi(OTf)3

Bi(OTf)(3) was proven to act as an effective catalyst for tandem ene-reaction/hydroamination of amino-olefin and amino-allene compounds with some enophiles, giving rise to functionalized N-heterocycles in good yields.     

Highly enantioselective (OC)Ru(salen)-catalyzed sulfimidation using N-alkoxycarbonyl azide as nitrene precursor

Enantioselective imidation of alkyl aryl sulfides with N-alkoxycarbonyl azide as a nitrene precursor was effected by using (OC)Ru(salen) complex 1 as catalyst. The steric and electronic nature of the N-alkoxycarbonyl group was found to strongly affect the enantioselectivity and the reaction rate, and high enantioselectivity (up to 99% ee) and good chemical yields were achieved by using 2,2,2-trichloro-1,1-dimethylethoxycarbonyl azide as the nitrene precursor at room temperature.     

Ferrimagnetic order in the mixed garnet (Y1− x Gd x )3Fe5O12

Ferrimagnetic order in the mixed rare-earth iron garnet (Y₁?_?? _x Gd _x )₃Fe₅O₁₂ system has been reinvestigated to cover the temperature range 5.0 to 700?K. The magnetization versus temperature exhibits a systematic variation with changing concentration x. The ferric-ion exchange coupling is strong enough to determine the Curie temperature ≈559?K for all the values x. The compensation temperature at which the magnetization crosses zero (shows the minimum) demonstrates the applicability of the three-sublattice model. The magnetic moment at 5.0?K indicates reasonable agreement with the relation n _B?=?|21x???5.0|μ_B for the (Y₁?_?? _x Gd _x )₃Fe₅O₁₂ system. The compensation temperature decreases with decreasing x from 1.0 and reaches zero near x?=?0.24. An enlargement of coercive force in the hysteresis loop for the low-field M-H curve is clearly seen in near the compensation temperature, indicating that a single domain is formed and the rotation of this single domain occurs without building up a multidomain structure.     

Chromatographic characterization of hydrophilic interaction liquid chromatography stationary phases: hydrophilicity, charge effects, structural selectivity, and separation efficiency

Fourteen commercially available particle-packed columns and a monolithic column for hydrophilic interaction liquid chromatography (HILIC) were characterized in terms of the degree of hydrophilicity, the selectivity for hydrophilic-hydrophobic substituents, the selectivity for the regio and configurational differences in hydrophilic substituents, the selectivity for molecular shapes, the evaluation of electrostatic interactions, and the evaluation of the acidic-basic nature of the stationary phases using nucleoside derivatives, phenyl glucoside derivatives, xanthine derivatives, sodium p-toluenesulfonate, and trimethylphenylammonium chloride as a set of samples. Principal component analysis based on the data of retention factors could separate three clusters of the HILIC phases. The column efficiency and the peak asymmetry factors were also discussed. These data on the selectivity for partial structural differences were summarized as radar-shaped diagrams. This method of column characterization is helpful to classify HILIC stationary phases on the basis of their chromatographic properties, and to choose better columns for targets to be separated. Judging from the retention factor for uridine, these HILIC columns could be separated into two groups: strongly retentive and weakly retentive stationary phases. Among the strongly retentive stationary phases, zwitterionic and amide functionalities were found to be the most selective on the basis of partial structural differences. The hydroxyethyl-type stationary phase showed the highest retention factor, but with low separation efficiency. Weakly retentive stationary phases generally showed lower selectivity for partial structural differences.     

Dynamic instability of a wheel moving on a discretely supported infinite rail

The parametric instability of a wheel moving on a discretely supported rail is discussed. To achieve this, an analysis method is developed for a quasi-steady-state problem which can represent an exponential growth of oscillation. The temporal Fourier transform of the rail motion is expanded by a Fourier series with respect to the longitudinal coordinate, and then the response of the rail deflection due to a quasi-harmonic moving load is derived. The wheel/track interaction is formulated by the aid of this function and reduced to an infinite system of linear equations for the Fourier coefficients of the contact force. The critical velocities between the stable and unstable states are calculated based on the nontrivial condition of the homogeneous matrix equation. Through these analyses the influences of the modeling of rail and rail support on the unstable speed range are examined. Moreover, not only the first instability zone but also other zones are evaluated.