Mixing automorphisms of compact groups and a theorem of Schlickewei

Summary We prove that every mixing ^d by automorphisms of a compact, connected, abelian group is mixing of all orders.Oblatum 5-II-1992The second author gratefully acknowledges support from NSF grant DMS-91-03056 at the Ohio State University     

微芯片电泳与电感耦合等离子体质谱的连接技术研究

研究了基于微芯片电泳分离和电感耦合等离子体质谱的连接技术,并对不同形态的Cu和As进行了快速分离和检测.     

Nitrato- and fluoroboracites M3B7O13NO3 and M3B7O13F

New boracites containing nitrato- or fluoroanions that appear to be true low-pressure phases have been synthesized at superatmospheric pressures. The M₃B₇O₁₃NO₃ compounds (M = Co, Ni, Cu, Zn, Cd) transform rapidly and reversibly in the temperature region 300–500°C between probable orthorhombic and face centered cubic symmetry, while the M₃B₇O₁₃F compounds (M = Mg, Mn, Fe, Co, Zn) appear to maintain rhombohedral symmetry up to their decomposition temperatures of 800–900°C. True high-pressure boracite-like phases containing F and Cr, Mn, Fe, or Co that decompose upon heating to M₃B₇O₁₃F have also been isolated.     

拟薄水铝石/陶瓷胶态加工浆料的流变性能

用拟薄水铝石纳米胶粒分散微米二硼化钛形成固含量为60Wt%的稳定陶瓷浆料,实验考察了拟薄水铝石固含量、二硼化钛固含量、温度对浆料流变性、稳定性的影响,对纳米γ-AlOOH胶粒分散微米TiB2的机制进行了讨论.大小约20nm的γ-AlOOH颗粒相互网联,成为外加微米陶瓷颗粒的骨架.浆料粘度随二硼化钛固含量的增加而增大,温度升高有利于胶体中薄水铝胶团与二硼化钛颗粒的相互作用并促进分散.     

Tritium volume activity in natural waters of the NPP Temelín region

With the use of the tritium monitoring network the samples of river water, air humidity and precipitation are collected and analysed for HTO in the vicinity of Temelín nuclear power plant.     

Ab initio calculation of the C/D ratio of magnetic circular dichroism

A procedure for calculating the magnetic circular dichroism C/D ratio from density functional theory calculations is discussed. The method is simplified considerably through the application of group theory and the irreducible-tensor method and only requires integrals of the magnetic dipole moment operator over a few orbitals and published tables of symmetry factors. The implementation of the method is tested through application to several small and medium-sized molecules.     

Metal-catalyzed di-tert-butylsilylene transfer: synthesis and reactivity of silacyclopropanes

Metal-catalyzed di-tert-butylsilylene transfer was developed as a mild, operationally simple, functional-group-tolerant method for silacyclopropane formation. Di-tert-butylsilylene was transferred from cyclohexene silacyclopropane 1 to an alkene through the use of a metal salt. Silacyclopropanation occurred at temperatures as low as -27 degrees C when AgOTf or AgOC(O)CF(3) were used as catalysts. Complex silacyclopropanes were formed stereospecifically and diastereoselectively from functionalized alkenes. Silacyclopropanes reacted with various carbonyl compounds, including aldehydes, ketones, formate esters, and formamides, in an overall process that efficiently converts alkenes into oxasilacyclopentanes with defined stereochemistry.     

Zur komplexchemie von 4-zentren-π-systemen : VIII. ESR-untersuchungen an heterobutadien-chelaten. I. Kalium-(diazabutadien-tetracarbonyl-metallate)

Glyoxal- and diacetyl-bis(imine)metal tetracarbonyls (RNCR′CR′NR)M(CO)₄ (M = Cr, Mo, W) are reduced with potassium in DME to give paramagnetic mono-anions. Their high-resolutior, ESR spectra show the hyperfine splittings of the magnetically active ligand atoms as well as the satellites of the metal isotopes ⁵³Cr,^95,97Mo and ¹⁸³W. The coupling constants are discussed with respect to π-bonding mechanisms.