Determination of tyrosine traces by adsorption voltammetry of its copper (II) complex

The electrochemical behavior of the copper-tyrosine complex has been studied by linear-sweep adsorption voltammetry. In 0.02 mol/L Na₂HPO₄ buffer solution (pH=9.6), the complex can be adsorped on a hanging mercury drop electrode and reduced at a peak potential of about –0.42 V (vs. SCE). The secondary derivative peak height is linear proportional to the concentration of tyrosine in the range 1.0×10^–7–5.0×10^–5 mol/L. The detection limit is 5×10^–8 mol/L.Project supported by the Provincial Science Foundation of Shandong Province     

Supramolecular self-assembly of polypseudorotaxanes in ionic liquid

The polypseudorotaxanes (PPRs) have been prepared by supramolecular self-assembly of β-cyclodextrins (β-CDs) threaded onto the triblock copolymers (Pluronic F127) in an ionic liquid [1-n-butyl-3-methylimidazolium hexafluorophosphate (bmimPF₆)] with two different manners. Structural characterizations of the assembled PPRs are carried out in detail respectively with XRD, ¹³C CP/MAS NMR, ¹H NMR and DSC techniques. The results obtained indicate a channel-type crystalline structure for such produced inclusion complexes (ICs). Which one will finally be included inside β-CD, F127 or bmimPF₆, is related to the ethanol amount around the initially β-CD/bmimPF₆ ICs. At higher ethanol concentration, F127 may squeeze bmimPF₆ molecules out from β-CD and thread themselves instead into the cavity of β-CD and finally precipitate with more CDs being stacked.     

AFM investigation of the {101} surface morphology of l-arginine trifluoroacetate (LATF) crystals

The {101} surface of l-arginine trifluoroacetate (LATF) crystals has been investigated by ex situ atomic force microscopy (AFM). The main step sources were observed in the form of growth spirals. The growth spirals are rounded and highly anisotropic. Microcrystals transferred from aggregates deposit at the step-edged on the facets. It is suggested that the microcrystals may lead to the formation of macrodefects during growth. Etching experiments reveal circular hollow cores, indicative of both screw dislocation growth, and negative crystals generated by further crystallization in the entrapped liquid inclusions are investigated.     

Investigations on adsorption potentiometry-part VIII. Determination of ultratrace copper in food by derivative adsorption chronopotentiometry

An electroanalytical method, based on derivative chronopotentiometry of the copper complex with 4-[(4-diethylamino-2-hydroxyphenyl) azo]-5-hydroxy-naphthalene-2,7-disulphonic acid (Beryllon III) accumulated on the surface of a hanging mercury drop electrode, for determining trace copper in food has been developed. The dependence of the peak height of reduction of the copper complex on the preconcentration time and preconcentration potential are discussed. Optimum experimental conditions include 0.01 M HOAc, 0.01M NaOAc, 1.0 x 10(-6) Beryllon III and a preconcentration potential of 0.10 V (vs. SCE). Under these conditions the detection limit and the linear range are 4 x 10(-11)M and 6 x 10(-11) -4 x 10(-7)M, respectively. The method was applied to samples of digested rice.     

Spectroscopic fingerprints of valence and spin states in manganese oxides and fluorides

We performed a systematic study of soft X-ray absorption spectroscopy in various manganese oxides and fluorides. Both Mn L-edges and ligand (O and F) K-edges are presented and compared with each other. Despite the distinct crystal structure and covalent/ionic nature in different systems, the Mn-L spectra fingerprint the Mn valence and spin states through spectral lineshape and energy position consistently and evidently. The clear O- and F-K pre-edge features in our high resolution spectra enable a quantitative definition of the molecular orbital diagram with different Mn valence. In addition, while the binding energy difference of the O-1s core electrons leads to a small shift of the O-K leading edges between trivalent and quadrivalent manganese oxides, a significant edge shift, with an order of magnitude larger in energy, was found between divalent and trivalent compounds, which is attributed to the spin exchange stabilization of half-filled 3d system. This shift is much enhanced in the ionic fluoride system. This work provides the spectroscopic foundation for further studies of complicated Mn compounds.     

Giant magnetoresistance:history,development and beyond

With the discovery of giant magnetoresistance(GMR),research effort has been made to exploiting the influence of spins on the mobility of electrons in ferromagnetic materials and/or artificial structures,which has lead to the idea of spintronics.A brief introduction is given to GMR effects from scientific background to experimental observations and theoretical models.In addition,the mechanisms of various magnetoresistance beyond the GMR are reviewed,for instance,tunnelling magnetoresistance,colossal magnetoresistance,and magnetoresistance in ferromagnetic semiconductors,nanowires,organic spintronics and non-magnetic systems.     

Theoretical study of the thermal rearrangement of chloromethylsilanes, and its mechanism

The thermal rearrangement reactions of chloromethylsilane, (chloromethyl)dimethylsilane, and (chloromethyl)vinylsilane have been studied by use of the density functional theory method at the B3LYP/6-311G(d, p) level. The structures of the reactants, transition states, and the products were determined and fully optimized. The geometries of the different stationary points and the harmonic vibrational frequencies were calculated at the same level. The results showed that thermal rearrangement of the chloromethylsilanes occurred via one pathway. The chlorine atom migrated from the carbon atom to the silicon atom, and the hydrogen atom migrated simultaneously from the silicon atom to the carbon atom through a double-three-membered-ring transition state, forming methylchlorosilane, trimethylchlorosilane, and vinylmethylchlorosilane. The energy barriers of the three rearrangements calculated at the B3LYP/6-311G(d, p) level were 217.4, 201.6, and 208.7 kJ mol^?1, respectively. The effects of alkyl substituents on silicon atom are discussed. Changes of thermodynamic functions, equilibrium constant, and reaction rate constant were calculated in accordance with Eyring transition-state theory over the temperature range 400–1,500 K.     

LD side-pumped Nd:GGG CW laser operating at 1110 and 1105 nm dual wavelengths and 1110 nm single wavelength

A diode-side-pumped continuous-wave Nd:GGG laser operating at dual-wavelength (1110 and 1105 nm) and single wavelength of 1110 nm is demonstrated for the first time. The maximum output power of the 1110 and 1105 nm dual-wavelength operation is 13.2 W. By adjusting the orientation of an insertion mirror, the relative intensities of the two wavelengths can be changed. Thus single wavelength operation at 1110 nm is obtained, and the output power is 9.6 W.     

Measurements of decays into and

Based on a sample of 5.8×10⁷ J/ψ events taken with the BESII detector, the branching fractions of J/ψ→2(π⁺π⁻)η and J/ψ→3(π⁺π⁻)η are measured for the first time to be (2.26±0.08±0.27)×10⁻³ and (7.24±0.96±1.11)×10⁻⁴, respectively.