On facets existed on concave interfaces in Czochralski-grown GaSb crystals

It is tried to make facet regions grow on interfaces curved concavely toward the melt using the Czochralski method. By increasing rapidly the pulling rate of crystals, the whole growth interface is once remelted and a concave interface is formed in the following growth process. A facet region occurs from a (¯I¯I¯I) plane which appears by the remelt of interfaces. This facet continues to grow while it is being surrounded by concave interfaces of nonfacet regions. From the microscopic measurement of spreading resistance. the impurity concentration is higher in the facet region than in non-facet ones. This suggests that the growth mechanism of the facet on concave interfaces is the same as that on convex ones.     

Efficient deanilidation of phosphoranilidates by the use of nitrites and acetic anhydride

Reagent systems of sodium– and tetrabutylammonium nitrite–acetic anhydride were proved to be extremely efficient for the deanilidation of nucleoside 3′-phosphoranilidates, whose reactions were rapid with the former and instant with the latter. It was further found that the reagent system is applicable to oligonucleotide synthesis provided that the exocyclic amino groups of 2′-deoxyadenosine, 2′-deoxyguanosine, and 2′-deoxycytidine were protected by succinylation.     

Short Radiative Lifetime and Non-Triplet Sensitization in Near-Infrared-Luminescent Yb(III) Complex with Tripodal Schiff Base

We prepared Ln(III) (Ln=Eu, Gd, and Yb) complexes with a tripodal Schiff base, tris[2-(5-methylsalicylideneimino)ethyl]amine (H₃L) and studied their photophysical properties. Upon ligand excitation, YbL showed Yb(III)-centered luminescence in the near-infrared region. While the overall quantum yield (0.60(1)%) of YbL in acetonitrile was moderate among the reported values for Yb(III) complexes, its radiative lifetime (0.33(2) ms) was significantly shorter than those reported previously. We propose that the ligand-to-metal charge-transfer (LMCT) state mediated the sensitization in YbL. The emission and excitation spectra of EuL indicated the participation of the LMCT state in the sensitization. The radiative lifetime (0.84(7) ms) for EuL in the solid state was rather short compared to those of reported Eu(III) complexes. Our results show that the Yb(III) complex with the Schiff base ligand has two features: the short radiative lifetime and the non-triplet sensitization path.     

铁催化2-烯基氮杂芳烃的绿色合成

以廉价、低毒的醋酸亚铁为催化剂,在三氟乙酸助催化下,2-甲基氮杂芳烃与芳香醛经过加成与脱水反应,直接选择性合成具有生物活性的反式2-烯基氮杂芳烃化合物,水是唯一副产物.该合成方法催化剂用量少,后处理方便,产率高,选择性高,底物适用范围广.治疗哮喘药顺尔丁中间体(E)-3-[2-(7-氯-2-喹啉基)乙烯基]苯甲醛(3v)的克级合成展现了该方法的应用前景.     

Two-dimensional hydrophilic interaction chromatography coupling anion-exchange and hydrophilic interaction columns for separation of 2-pyridylamino derivatives of neutral and sialylated N-glycans

A novel chromatographic approach coupling anion-exchange (diethylaminoethylene) and hydrophilic-interaction (amide or zwitterionic type) columns was developed for the separating of 2-pyridylamino derivatives of N-glycans (PA-N-glycans). This is a kind of on-line, two-dimensional (2D) separation approach in hydrophilic-interaction chromatography (called the 2D-HILIC method), analogous to that of coupling cation- (or anion-, or mixed ion-) exchange and reversed-phase columns in hydrophobic interaction (reversed-phase) chromatography. The efficiency of the 2D-HILIC method was tested with biantennary neutral and sialylated PA-N-glycan standards by properly combining linear gradient elutions of water-acetonitrile and spiked-salt (ammonium acetate) elutions. The retention time RSDs of all the peaks in three sequential runs of a 100 min cycle are less than 0.52%, which indicates a reasonably good repeatability of the 2D-HILIC method. Then, the method was applied to a complex mixture of PA-N-glycans from human serum proteins. It was demonstrated that the neutral PA-N-glycans and mono-, di-, tri-, and tetrasialylated PA-N-glycans are able to be eluted in turn according to the number of sialic acids in an automated (programmed) single run.     

A Delayed HIV Infection Model with the Homeostatic Proliferation of CD4+ T Cells

In this paper, we investigate a delayed HIV infection model that considers the homeostatic proliferation of CD4⁺ T cells. The existence and stability of uninfected equilibrium and infected equilibria(smaller and larger ones) are studied by analyzing the characteristic equation of the system. The intracellular delay does not affect the stability of uninfected equilibrium, but it can change the stability of larger positive equilibrium and Hopf bifurcation appears inducing stable limit c...     

Neutron electric dipole moment measurement with a buffer gas comagnetometer

A neutron EDM measurement with a comagnetometer is discussed. For magnetometry, polarized xenon atoms are injected into a cylindrical cell where a cylindrically symmetric magnetic field and an electric field are applied for the EDM measurement. The geometric phase effect (GPE), which originates from particle motion in a magnetic field gradient, is analyzed in terms of the Dyson series. The motion of the xenon atom is largely suppressed because of a small mean free path. The field gradient is controlled by means of NMR measurements, where the false effect of Earth?s rotation is removed. As a result, the GPE is reduced below 10⁻²⁸e cm${10}^{-28}e\text{cm}$.     

Low Power Penalty Operation of a Wide Input Dynamic Range Cross-Phase Modulation Wavelength Converter

We successfully demonstrated low power penalty operation of a cross-phase modulated (XPM) wavelength converter using a semiconductor optical amplifier (SOA) power equalizer. We also clarified the SOA equalizing level for more adaptive wavelength conversion and achieved a power penalty of less than 1 dB over the wide input dynamic range of 15 dB.     

Ion–ion interactions of LiPF6 and LiBF4 in propylene carbonate solutions

Self-diffusion coefficients of Li⁺ D_Li⁺, PF₆⁻ D_PF6⁻ and solvent propylene carbonate (PC) D_PC in LiPF₆−PC solutions were determined at 298 K by the pulse gradient spin echo (PGSE) NMR technique over the salt concentration range of 0.1–3.0 M (M = mol dm^– 3). The order of the diffusion coefficients was found to be D_Li⁺ < D_PF6⁻ < D_PC over the concentration range examined, and they were monotonically decreased with increasing the salt concentration. Haven ratio Λ/Λ_NMR, where Λ and Λ_NMR represent the ionic conductivity measured electrochemically and that estimated via the Nernst-Einstein equation using the diffusion coefficient, respectively, was evaluated as the measure of the ion–ion interaction in the LiPF₆–PC solutions. Though Λ/Λ_NMR values for LiPF₆-solutions decrease with increasing the salt concentration, they were greater than those for LiBF₄–PC solutions over the whole concentration range examined, which indicates that the ion pair formation ability of PF₆^– ion is weaker than that of the BF₄^– ion. The smaller value of the ionic conductivity for the highly concentrated LiPF₆–PC solution (above 2.0 M) than that of the LiBF₄-solutions can be attributed to the more rapidly increased viscosity relative to the LiBF₄-solution. Classic molecular dynamics (MD) simulations for the respective LiPF₆ and LiBF₄-solution of 0.5 and 1.0 M were also carried out based on the effective pair potentials. Diffusion coefficients, ionic conductivity and Haven ratio for these solutions were calculated from MD trajectories, and they qualitatively agree with those evaluated by experiments. Pair correlation functions g_LiO(r) (for Li⁺–O (PC) pair) and g_LiPF6(r) (for Li⁺–PF₆^– pair) or g_LiBF4(r) (for Li⁺–BF₄^– pair) revealed that the lithium ion weakly forms the contact ion pairs with PF₆^–, whilst strongly with BF₄^–, which supports the present experimental results. Moreover, the simulation results show that both anions in the contact ion pairs predominantly take the monodentate form, which is in contrast to the multidentate coordination predicted by ab initio calculation in gas phase.