Crystal structure and magnetic properties of two new cobalt selenite halides: Co5(SeO3)4X2 (X=Cl, Br)

Two new isostructural cobalt selenite halides Co₅(SeO₃)₄Cl₂ and Co₅(SeO₃)₄Br₂ have been synthesized. They crystallize in the triclinic system space group P−1 with the following lattice parameters for Co₅(SeO₃)₄Cl₂: a=6.4935(8) Å, b=7.7288(8) Å, c=7.7443(10) Å, α=66.051(11)°, β=73.610(11)°, γ=81.268(9)°, and Z=1. The crystal structures were solved from single-crystal X-ray data, R1=3.73 and 4.03 for Co₅(SeO₃)₄Cl₂ and Co₅(SeO₃)₄Br₂, respectively. The new compounds are isostructural to Ni₅(SeO₃)₄Br₂.Magnetic susceptibility measurements on oriented single-crystalline samples show anisotropic response in a broad temperature range. The anisotropic susceptibility is quantitatively interpreted within the zero-field splitting schemes for Co²⁺ and Ni²⁺ ions. Sharp low-temperature susceptibility features, at T_N=18 and 20 K for Co₅(SeO₃)₄Cl₂ and Co₅(SeO₃)₄Br₂, respectively, are ascribed to antiferromagnetic ordering in a minority magnetic subsystem. In isostructural Ni₅(SeO₃)₄Br₂ magnetically ordered subsystem represents a majority fraction (T_N=46 K). Nevertheless, anisotropic susceptibility of Ni₅(SeO₃)₄Br₂ is dominated at low temperatures by a minority fraction, subject to single-ion anisotropy effects and increasing population of S_z=0 (singlet) ground state of octahedrally coordinated Ni²⁺.     

Bacteria counting with impedance spectroscopy in a micro probe station

A method to quantify the density of viable biological cells in suspensions is presented. The method is implemented by low-frequency impedance spectroscopy and based on the finding that immobilized ions are released to move freely in the surrounding suspension when viable Escherichia coli cells are killed by a heat shock. The presented results show that an amount of ions corresponding to approximately 2 x 10(8) unit charges are released per viable bacterium killed. A micro probe station with coplanar Ti electrodes was electrically characterized and used as a measuring unit for the impedance spectroscopy recordings. This unit is compatible with common microfabrication techniques and should enable the presented method to be employed using a flow-cell device for viable bacteria counting in miniaturized on-line monitoring systems.     

Precision Penning trap mass measurements of rare isotopes produced by projectile fragmentation

The low-energy beam and ion trap facility LEBIT at NSCL/MSU is at present the only facility where precision experiments are performed with stopped rare isotope beams produced by fast-beam fragmentation. LEBIT combines high-pressure-gas stopping with advanced ion manipulation techniques to provide brilliant low-energy beams. So far these beams have mainly been used for mass measurements on short-lived rare isotopes with a 9.4T Penning trap mass spectrometer. Recent examples include ^70m Br , located at the proton dripline, ³²Si and the iron isotopes ^63-65Fe . While the measurement of ³²Si helps to solve a long-standing dispute over the validity of the isobaric multiplet mass equation (IMME) for the A = 32 , T = 2 multiplet, the mass measurements of ^65m,g Fe marked the first time a nuclear isomeric state has been discovered by Penning trap mass spectrometry.     

Multicomponent analysis of drinking water by a voltammetric electronic tongue

A voltammetric electronic tongue is described that was used for multicomponent analysis of drinking water. Measurements were performed on drinking water from a tap and injections of the compounds NaCl, NaN₃, NaHSO₃, ascorbic acid, NaOCl and yeast suspensions could be identified by use of principal component analysis (PCA). A model based on partial least square (PLS) was developed for the simultaneously prediction of identification and concentration of the compounds NaCl, NaHSO₃ and NaOCl. By utilizing this type of non-selective sensor technique for water quality surveillance, it will be feasible to detect a plurality of events without the need of a specific sensor for each type of event.     

Perthio- and perseleno-1,3-butadienes, -but-1-ene-3-ynes,and -[3]-cumulenes: one-step syntheses from 1,4-dilithio-1,3-butadiyne

[reaction: see text] Treatment of 1,4-dilithio-1,3-butadiyne (1) with dichalcogenides RSSR or RSeSeR affords dithio- and diseleno-1,3-butadiynes (2, 3), perthio- and perseleno-[3]-cumulenes (4, 5), perthio- and perseleno-1,3-butadienes (6, 7), and/or perthio- and perseleno-but-1-ene-3-ynes (8, 9). The products can be controlled by stoichiometry and temperature, by the presence or absence of oxygen, and by choice of the "R" group. By X-ray crystallography, hexa(methylthio)-1,3-butadiene is highly twisted, with a torsion angle [Phi(CCCC)] of 84.7 degrees and an elongated C(2)-C(3) distance of 1.484(3) A.     

钨离子团簇与N2分子的反应性

利用激光蒸发团簇源产生Wn团簇束,团簇束通过一个充有N2气体分 子的低压反应池,利用飞行时间质谱探测反应产物,在类单次碰撞条件下研究了W+10 -W+50和N2分子的反应性,在室温条件下测量了N2分子与W+n团簇反应的 反应几率。团簇尺寸在10～26原子的团簇与N2分子的反应几率与团簇尺寸有很强的相关性 ,对n=16,22,23的团簇具有比较高的反应性。W+n与N2分子的反应性与Wn与N 2分子的反应性显示出相似的规律性。     

Two new layered oxohalides in the system Cu–Yb–Te–O–Cl

Two complex lanthanide(III) transition metal(II) tellurium(IV) oxyhalides, Cu₃Yb₂(TeO₃)₄Cl₄ and Cu₃Yb₃(TeO₃)₄Cl₆ have been synthesized and the crystal structures were determined by single-crystal X-ray diffraction. Both compounds are layered with only weak connections in between the layers. The layers are made up of [YbO₈], [TeO₃] and [CuO_xCl_y] polyhedra. In both compounds the strong Lewis acid cations Yb³⁺ and Te⁴⁺ only form bonds to oxygen while Cu²⁺ form bonds to both oxygen and chlorine. This leads the Cl^? ions to be expelled from the bonding volumes of the crystal structures and protrude from the layers. Magnetic susceptibility measurements were performed on a powder sample of Cu₃Yb₂(TeO₃)₄Cl₄. The Curie–Weiss law found at low temperatures indicates a Curie–Weiss temperature of ca. ?5(1) K. However, indication for long-range magnetic ordering could not be observed down to 1.87 K. The two new phases are to the best of our knowledge the first containing all three of Cu, Yb and Te.     

Dimethylformamide as a carbon monoxide source in fast palladium-catalyzed aminocarbonylations of aryl bromides

Dimethylformamide (DMF) acts as an efficient source of carbon monoxide and dimethylamine in the palladium-catalyzed aminocarbonylation (Heck carbonylation) of p-tolyl bromide to provide the dimethylamide. Addition of amines to the reaction mixture in excess delivers the corresponding aryl amides in good yields. The amines employed, benzylamine, morpholine, and aniline, all constitute good reaction partners. The reaction proceeds smoothly with bromobenzene and more electron-rich aryl bromides, but electron-deficient aryl bromides fail to undergo aminocarbonylation. The reactions are conducted at 180-190 degrees C for 15-20 min with microwave heating in a reaction mixture containing imidazole and potassium tert-butoxide: the latter is required to promote decomposition of the DMF solvent at a suitable rate. The beneficial effects of controlled microwave irradiation as an energy source for the rapid heating of the carbonylation reaction mixture are demonstrated. The carbonylation procedure reported herein, which relies on the in situ generation of carbon monoxide, serves as a convenient alternative to other carbonylation methods and is particularly applicable to small-scale reactions where short reaction times are desired and the direct use of carbon monoxide gas is impractical.     

A characterization of adding machine maps

Let f :X→X be a continuous map of a compact metric space to itself. We prove that f is topologically conjugate to an adding machine map if and only if X is an infinite minimal set for f and each point of X is regularly recurrent. Moreover, if X is an infinite minimal set for f and one point of X is regularly recurrent, then f is semiconjugate to an adding machine map.