Novel stereoselective entry to 2'-beta-carbon-substituted 2'-deoxy-4'-thionucleosides from 4-thiofuranoid glycals

2'-Beta-methyl- and 2'-beta-hydroxymethyl-2'-deoxy-4'-thionucleosides have been synthesized through PhSeCl-mediated electrophilic glycosidation using 4-thiofuranoid glycals having carbon substituents at the C2-position as a glycosyl donor. Preparation of these glycals were carried out by means of the C2 lithiation of 1-chloro-4-thiofuranoid glycal with LTMP followed by the Birch reduction of the chlorine atom. [reaction: see text]     

Non-destructive analysis of the two subspecies of African elephants, mammoth, hippopotamus, and sperm whale ivories by visible and short-wave near infrared spectroscopy and chemometrics

Visible (VIS) and short-wave near infrared (SW-NIR) spectroscopy was used for non-destructive analysis of ivories. VIS-SW-NIR (500-1000 nm) spectra were measured in situ for five kinds of ivories, that is two subspecies of African elephants, mammoth, hippopotamus, and sperm whale. Chemometrics analyses were carried out for the spectral data from 500 to 1000 nm region. The five kinds of ivories were clearly discriminated from each other on the scores plot of two principal components (PCs) obtained by principal component analysis (PCA). It was noteworthy that the ivories of the two subspecies of African elephants were discriminated by the scores of PC 1. The loadings plot for PC 1 showed that the discrimination relies on the intensity changes in bands due to collagenous proteins and water interacting with proteins. It was found that the scores plot of PC 2 is useful to distinguish between the ivories of the two subspecies of African elephants and the other ivories. We also developed a calibration model that predicted the specific gravity of five kinds of ivories from their VIS-SW-NIR spectral data using partial least squares (PLS)-1 regression. The correlation coefficient and root mean square error of cross validation (RMSECV) of this model were 0.960 and 0.037, respectively.     

Efficient 355-nm generation in CsB3O5 crystal

We demonstrate UV generation in CSB3O5 (CBO) crystals grown by the top-seeded solution growth technique. 355-nm UV light was generated by use of a type II CBO crystal as a sum frequency of the fundamental light and the second harmonic of a nanosecond Nd:YVO4 laser. A 3.0-W output of the third-harmonic was obtained at a repetition rate of 31 kHz. The conversion efficiency from the fundamental light to the third harmonic reached 30%, which was 1.5 times higher than that obtained with a type II LiB3O5 crystal under the same experimental conditions.     

Beam-polarization asymmetries for the p(gamma-->, K+)Lambda and p(gamma-->, K+)Sigma(0) reactions for E(gamma)=1.5-2.4 GeV

Beam polarization asymmetries for the p(gamma-->,K+)Lambda and p(gamma-->,K+)Sigma(0) reactions are measured for the first time for E(gamma)=1.5-2.4 GeV and 0.6相似文献   

Electronic control of spin alignment in pi-conjugated molecular magnets

Intramolecular spin alignment in pi-conjugated molecules is studied theoretically in a model of a Peierls-Hubbard chain coupled with two localized spins. By means of the exact diagonalization technique, we demonstrate that a spin singlet (S=0) to quartet (S=3/2) transition can be induced by electronic doping, depending on the chain length, the positions of the localized spins, and the sign of the electron-spin coupling. The calculated results provide a theoretical basis for understanding the mechanism of spin alignment recently observed in a diradical donor molecule.     

One Dimensional Face-to-Face Stacking of Anderson–Evans [Cr(OH)6Mo6O18]3− Polyoxometalate Anion: Synthesis, Structure, and Physical Properties of (BEDT-TTF)4[Cr(OH)6Mo6O18]⋅2H2O

The synthesis, structural and magnetic characterizations of a new charge transfer salt (BEDT-TTF)₄[Cr(OH)₆Mo₆O₁₈]2H₂O based on the planar paramagnetic Anderson–Evans polyoxometalate are reported. Structural parameters: T=293 K, triclinic (P ), a=5.9545(2) Å, b=16.3767(6) Å, c=21.8643(6) Å, =110.829(2)°, =91.262(2)°, =98.129(1)°, Z=1, R=0.0540. The crystal structure is characterized by a face-to-face stacking of the anions giving rise to a one-dimensional inorganic chain which develops along the a direction. The organic layers contain two crystallographically independent BEDT-TTF dimers that form alternating stacks along the b direction. This organic chain is perpendicular to the inorganic chains. The charges on BEDT-TTF dimers are deduced to +1.2(1) and +1.7(1) on the basis of the intramolecular bond lengths. The EPR spectrum at 2.5 K is characterized by the superposition of BEDT-TTF⁺ and [Cr^III(OH)₆Mo₆O₁₈]^3– signals. The static susceptibility can be fitted by the Curie–Weiss law down to 1.9 K and the magnetic moment at 300 K is estimated to 4.21 _B , suggesting the uncorrelated spin system with BEDT-TTF⁺ (S=1/2) and Cr^III (S=3/2) ions. This interpretion is consistent with the charge disproportionation on BEDT-TTF dimers along the stack, which is supported by the refined molecular structure and is closely related to the insulating behavior (<10^–9Scm^–1 at RT).     

Novel fluorescent isoquinoline pigments, panaefluorolines A-C from the cultured mycobiont of a lichen, Amygdalaria panaeola

Novel fluorescent substances, named panaefluorolines A-C (1-3), were isolated from the cultured mycobiont of a lichen, Amygdalaria panaeola. These structures were elucidated on the basis of spectroscopic data, especially 2D NMR.     

Histone core slips along DNA and prefers positioning at the chain end

We studied the stability and dynamics of a model of a nucleosome, the fundamental unit for the packing of long DNA in eukaryotes, using a Brownian dynamics simulation. For the proper folding of a stiff polymer on a core particle, moderate attractive interaction is shown to be essentially important, which explains the empirical experimental protocol for the reconstitution of nucleosomes. The effect of the chain end on the positioning of the core particle is examined and compared with the experimental data by atomic force microscopy measurement. It is also suggested that the core particle exhibits sliding motion along the chain as a manifestation of Brownian motion.