Reductive coupling of carbonyl compounds using lanthanum metal

We found that lanthanum metal was an excellent agent for the reduction of carbonyl compounds in the presence of a catalytic amount of iodine. When carbonyl compounds were treated with lanthanum metal in the presence of a catalytic amount of iodine, the reductive coupling of the carbonyl compounds proceeded efficiently to afford the corresponding vic‐diols in moderate to good yields. © 2000 John Wiley & Sons, Inc. Heteroatom Chem 11:81–85, 2000     

The correlation between charge and energy flow within cascade models for quark and hadron jets

We consider the ratio \(\frac{{\Delta Q}}{{\Delta \varepsilon }}\) of the charge and energy fraction carried by particles in the angular interval ΔΩ with respect to the jet axis, where we assume a recursive scheme for the hadron cascade. A measurement of this ratio inep andvp collisions determines the quark chargeQ _q at any angle ΔΩ and ine ⁺ e ^?-annihilations alsoQ _q ⁴ can be obtained. In hadron hadron collisions this ratio discriminates in a very direct way between different production models. We consider the “stopping quark” model, the “two dual sheet” model, and finally a leading cluster model. More data on \(\frac{{\Delta Q}}{{\Delta \varepsilon }}\) would be desirable at higher energies in particular for meson beams.     

Recoil effect of photoelectrons in the Fermi edge of simple metals

High energy resolution photoelectron spectroscopy of conduction electrons in the vicinity of the Fermi edge in Al and Au at excitation energies of 880 and 7940 eV was carried out using synchrotron radiation. For the excitation energy of 7940 eV, the observed Fermi energy of Al shows a remarkable shift to higher binding energy as compared with that of Au, with accompanying broadening. This is due to the recoil effect of the emitted photoelectrons. The observed spectra are well reproduced by a simple model of Bloch electrons based on the isotropic Debye model.     

Pd(0)‐catalyzed polycondensation of methyl propargyl carbonate and bisphenols under stoichiometrically imbalanced conditions

We found that a novel Pd(0)‐catalyzed polycondensation of methyl propargyl carbonate ( 1 ) and bisphenol analogs 4 such as 4,4′‐dihydroxydiphenyl ether (4b ) proceeded successfully and gave polyethers 5 having exomethylene groups. The polycondensation was affected by the kind of bisphenol analogs used. The molar ratio of 1 and 4 also affected the polymerization behavior. Polyethers 5 with higher molecular weights were obtained by polymerization with 0.5 equiv of 4 toward 1 . The use of 1 equiv of 4 gave poor results. When 4,4′‐dihydroxybenzophenone ( 4d ) was employed as a nucleophile, benzenesulfonamide ( 13 ) was needed as an additive for obtaining the corresponding polyether with higher molecular weight. The Pd(0)‐catalyzed condensation of 1 and p‐hydroxyacetophenone was conducted as a model reaction. The desired compound and three by‐products were produced. Two of the by‐products were formed by reaction of 1 and methanol liberated from 1 . The other one appeared to be formed via hydrogenolysis. The formation of the by‐products suggested that some terminal reactions took place in the polycondensation of 1 and 4 . © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2250–2261, 2008     

Slippage of nonsuperfluid helium films

We measured the mechanical response of 3He and 4He films on an oscillating substrate using an ultrasonic technique. Up to the coverage at which the fluid state appears at absolute zero, a part of the nonsuperfluid 3He and 4He films underwent slipping relative to the substrate at low temperatures. From the temperature dependence of the slippage, it was found that a thermally activated process plays an important role in the frictional force of this system.     

The reaction of hydrogen atoms with 1-butanethiol and thiolane the role of chemically activated 1-butanethiol

The reaction of 1-butanethiol with hydrogen atoms has been studied at temperatures of 295° and 576° K under the pressure of 660 Pa, using a conventional discharge-flow apparatus. The reaction products (besides hydrogen sulfide and methane) under the low conversion range (～10%) consisted mainly of n-butane, 1-butene, and propylene-propane, with the relative yields of 70, 25, and 5% at 295° K and 25, 50, and 10% at 576°K. Analysis of kinetic equations by numerical integration indicates that the following initial steps are consistent with the experimental results: where the following expressions have been derived for k₁ and k₂: The subsequent reaction of the butylthio radical with hydrogen atoms leads to the chemically activated 1-butanethiol which either stabilizes to 1-butanethiol or decomposes to 1-butene and hydrogen sulfide, depending on the experimental conditions. A similar analysis of the data on the thiolane-H system has yielded the following rate parameters for the initial step to form the 4-mercapto-1-butyl radical: .     

Synthesis of a novel C-6 nigrogen-substituted carbapenem from 6-aminopenicillanic acid

Synthesis of optically active 6-phthalimidocarbapenems from 6-aminopenicillanic acid is described.     

Novel method for linking CdS nanoparticles at liquid-liquid interface

Liquid-liquid interface of water-hexane provides a unique reaction environment in which CdS nanoparticles capped with mercaptoethylamine could be linked together to form a homodimer with a divalent acid chloride, sebacoyl chloride. Prior to the reaction, mercaptoethylamine-capped CdS in aqueous solution was purified by dialysis and freeze-drying. The observation with a transmission electron microscope suggested the formation of a homodimer of CdS nanoparticles.