Regio-controlled hydrogen-deuterium exchange of biologically important indoles under uv irradiation

Photochemical hydrogen-deuterium exchange reaction of biologically important indoles is reported. The regioselectivity of the photodeuteration was found to be controlled by the ammonium group of the side chain.     

Influence of the type of alkyl group on hydrolysis and polycondensation of tetraalkoxysilane

The early stage of hydrolysis and polycondensation of tetraalkoxysilanes (TAOS) in the closed TAOS-C₂H₅OH-H₂O-HCl system at 40°C was studied by the trimethylsilylation technique combined with the gas-liquid and gel permeation chromatographies. Tetramethoxy, tetraethoxy, tetra (n-propoxy) and tetra (n-butoxy) silanes were used as TAOS. The tendencies of variation with time in the distribution and molecular weight of silicate species in the solutions were almost the same in all the TAOS solutions, suggesting that the differences in the alkyl group of the TAOS had little effect on the hydrolysis and polycondensation.     

Two-dimensional measurement of laser-induced target movement by face-on interferometry

Initial movement of laser irradiated foil targets has been measured by face-on interferometry with two-dimensional resolution. This interferometric method provides direct and precise information about the initial movement of the rear surface of the target compared with conventional diagnostics. Target movement of 20–500 nm from the original position has been observed.     

Carbon-13 NMR chemical shift and electronic structure of polypeptide as studied by tight-binding MO theory: poly (β-benzyl L-aspartate) with the right-handle α-helix and left-handed α-helix forms

An attempt was made to calculate ¹³C NMR chemical shifts of poly(β-benzyl L-aspartate) having the right-handed α-helix (α_R-helix) and left-handed α-helix (α_L-helix) forms by a tight-binding MO sum-over-states theory within the extended Hückel framework, in order to examine whether or not the conformation-dependent ¹³C chemical shifts previously determined by the cross polarization-magic angle spinning technique are reproduced by a change of electronic structure of the polymer. It is found that the relative displacements of the observed C_α, C_β and carbonyl ¹³C chemical shifts between the α_R- and α_L-helices are reproduced qualitatively by the calculation.     

Cell culture on polymers prepared by radiation-induced polymerization of various glass-forming monomers

The growth of cells on polymers prepared by the radiation polymerization of monomethacrylate and dimethacrylate was investigated. Cell growth was affected greatly by such properties of the polymers as water content, wettability, and porosity. Growth was promoted remarkably by rinsing the polymers with warm water at 60-70 degrees C and by irradiation of polymers with an electron beam. Cell growth decreased with increasing oxyethylene length (n) in the polymerized dimethacrylate of same series, CH2C(CH3)CO(OCH2CH2)nOCOC(CH3)CH2. A decrease in the hydrophilicity of the polymer increased cell growth rate. Formation of pore structures in the polymer films also increased the cell growth.     

Synthesis and characterization of nickel(II) complexes with potentially pentadentate macrocyclic ligands having N3O2 donor set

Nickel(II) complexes of N₃O₂ donor macrocycles incorporating 17- to 19-membered macrocyclic rings have been prepared. Physical measurements ind     

Structure of holothurin A a biologically active triterpene-oligoglycoside from the sea cucumber holothuria leucospilota brandt

On the basis of chemical and physicochemical evidence, the structure of holothurin A, a biologically active major obligoglycoside o lanostane-type triterpene holothurigenol ($\text{2}$), has been elucidated to be $\text{8}$.