Laser-Induced Diffraction Rings from an Absorbing Solution

We observed multiple diffraction rings of a cw Ar⁺ laser beam from a nitrobenzene solution of saturable absorber BDN (bis-(4-dimethylaminodithiobenzil)-nickel) caused by the spatial self-phase modulation at low incident optical intensities. We obtained 37 rings for a 200-μm thick sample at an optical intensity of 38 W/mm². The refractive-index change Δ;n and effective nonlinear refractive index n₂ were determined from the number of observed rings and by the z-scan technique. We obtained large values of Δ;n∼0.1 and n₂ = -2.9×;10^-5 cm²/W. This large nonlinearity is attributed to a thermal effect resulting from linear absorption.     

Characterization of oligomeric polypropyleneglycol acrylate by GC, SFC and MALDI-TOF-MS.

Polypropyleneglycol acrylate (PGA), one of the typical acrylic oligomers manufactured industrially, was comprehensively characterized by gas chromatography (GC), supercritical fluid chromatography (SFC) and matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS). The homologous series of polypropyleneglycol diacrylate (DA), polypropyleneglycol monoacrylate (MA), and unreacted polypropyleneglycol (PG) were observed as Na adducts in the MALDI-MS spectra of the PGA samples. The relative intensities of these peaks reflect the distributions of the homologues, although their accurate quantification was generally difficult because of change in the ionization efficiency depending on the chemical structure and the molecular weight of the species. On the other hand, the DA and the MA homologues were observed in the chromatograms obtained by SFC in a temperature-programming mode, while the PG homologues were not detected under the given SFC conditions using UV detection. Here, the determination of the degree of polymerization of each component in the chromatograms was accomplished through SFC fractionation for the corresponding peaks, followed again by MALDI-TOF-MS measurement. Furthermore, most of the components in the PGA samples were almost completely separated in the resulting gas chromatograms, and their unequivocal assignments were made also using the retention data on the gas chromatograms of the SFC fractions. As for the quantitative analysis, the relative abundances among DA, MA and PG for lower degrees of polymerization can be easily calculated based on the observed gas chromatograms, whereas the distribution of DA and MA can be estimated from the observed SFC data even for the relatively higher molecular weight fractions, which are generally difficult to determine accurately by GC because of their lower volatility. These results demonstrated that even the complex PGA samples were able to be characterized in detail by using GC, SFC and MALDI-TOF-MS complementarily.     

Charge susceptibility and charge correlation function in the d---p model

The properties of the charge fluctuation are investigated in the d---p model with the repulsion U_pd between holes on the nearest-neighbor Cu and O sites and the infinite on-site repulsion U_d at the Cu site. We calculate the charge susceptibility χ^c(q, iω_n) and the charge correlation function S^c(q) = TΣ_ωn χ^c(q, iω_n). It is found that S^c(q) has a peak at the Γ point and a maximum in a ring around the Γ point. The former is due to Tχ^c(q, 0). Its intensity is proportional to temperature T and strongly enhanced by U_pd. The latter is due to TΣ_{ωn ≠ 0} χ^c(q, iω_n) and shows a weak T and U_pd dependence. The intensity of the diffuse X-ray scattering on taking the charge fluctuation into account is also calculated. The result is consistent with the experiments in La_2−δSr_δCuO₄.     

Spectroscopy of charmed baryons

We have fitted the masses and elastic widths of the S=0 baryons in the context of the QCD-improved quark shell model. All states in theN=0, 1, 2 and 3 harmonic oscillator bands have been included. Three models for the decay of these states have been studied, and it is concluded that the usual spectator model for the decays must be modified. Many resonances in theN=2 and 3 bands were found to decouple from the πN channel, supporting a previous solution to the missing resonance puzzle. No evidence has been found for the tensor force, while conflicting data exist for the 3-body spin orbit term. We also have found evidence that the contact force varies with band. The (56,1^?) multiplet is lower than expected.     

Vibrational analysis of ethylamines: Trans and gauche forms

Starting from force constant values calculated by an ab initio MO method ($\text{4-31G(N}{}^1\text{)}$), and by adjusting the diagonal elements, a practical force constant matrix (F) has been reached which could explain the observed infrared and Raman spectra (in the frequency range lower than 2000 cm^?1) of the gauche form of the ethylamine CH₃CH₂NH₂ molecule and five isotopic species CH₃¹³CH₂NH₂, CH₃CH₂¹⁵NH₂, CH₃CD₂NH₂, CH₃CH₂ND₂, and CD₃CD₂NH₂. The F matrix for the trans form of ethylamine was constructed by transferring ab initio $\text{4-31G(N}{}^1\text{)}$ values and by revising diagonal elements with conversion factors whose values are equal to the corresponding values of gauche form. A nearly complete set of assignments was achieved of the vibrational bands of ethylamines, observed so far in the spectral range 2000–100 cm^?1. In matrix isolation spectroscopy, two bands assignable to the NH₂ wagging vibrations of gauche and trans forms have been found at 775 and 782 cm^?1, respectively, for CH₃CH₂NH₂. They are at 768 and 774 cm^?1, respectively, for CD₃CD₂NH₂. From the intensity changes of these bands observed on changing the nozzle temperature in the matrix formation, the energy difference ΔE (gauche-trans) of these two conformers has been estimated to be 100 ± 10 cm^?1.     

Dual Focus Optical Head for 0.6 mm and 1.2 mm Disks

We propose a dual focus optical head with a holographic optical element (HOE) which corrects spherical aberrations in order to read both 0.6 mm disks and 1.2 mm disks. The thin disks are read using transmitted light and the thick disks are read using +1st order diffracted light of the blazed HOE. The good quality of the focused spots and the focusing error signals was experimentally confirmed. No influence of unnecessary diffracted light was observed.     

Improved high-speed counter-current chromatograph with three multilayer coils connected in series. II. Separation of various biological samples with a semi-preparative column

The semipreparative capability of the newly developed high-speed counter-current chromatograph equipped with a set of three multilayer coils has been demonstrated in separations of a variety of biological samples including triterpenoic acids, indole auxins, bacitracin, flavonoids and tetracycline derivatives, each with a suitable two-phase solvent system. The sample quantities ranging from 50 to 500 mg were efficiently separated within a few hours. The separation of tetracycline derivatives was remarkably improved by adding ammonium acetate to the solvent system.