Extractants selection for hyphenated electrothermal atomic absorption method

The theoretical approach for extractants selection during hyphenated atomic absorption determination of highly volatile metals (Pb, Cd), hydride- (Sb, Bi) and carbide-forming (Cr) metals using thermodynamic modelling was proposed. The calculated parameter — maximum pyrolysis temperature — can be used for selection of the extractants and chemical modifiers. Using this approach the antimony extract with Brilliant green was modified for which the 1.8-fold sensitivity and 2.6-fold repeatability decreasing while extract sampling in graphite furnace was observed. A chemical modifier — mixture of hydrazine nitrate with the palladium(II) complex with Xylenol orange — was theoretically selected and experimentally tested, which allowed to enhance the maximum pyrolysis temperature on 200°C, to eliminate extract matrix influence. Using this modifier two-fold increasing in sensitivity and 3-fold decreasing in relative standard deviation was achieved while extraction atomic absorption determination.      

Selective Benzoylation of 1-(β-D-Xylopyranosyl)-3,5-dimethylpyrazole

Abstract

Selective benzoylation of l-(β-d-xylopyranosyl)-3,5-dimethylpyrazole (1) has been performed to give 2,3,4-tri- (2), 3,4-di- (3), 2,4-di- (4), 3- (5) and 4-benzoate (6). The O-acetyl derivatives of compounds 3 and 4 (7, 8), di-O-acetyl of 5 and 6 (9, 10) and O-methanesulphonyl of 3 and 4 (11, 12) have been obtained. The relative reactivity of the hydroxyl groups of 1 was HO-4 ≥ HO-3 ? HO-2. The analysis of ¹ H NMR and ¹³C NMR spectra of 1-12 is presented.     

On solving the maximum clique problem

The Maximum Clique Problem (MCP) is regarded here as the maximization of an indefinite quadratic form over the canonical simplex. For solving MCP an algorithm based upon Global Optimality Conditions (GOC) is applied. Furthermore, each step of the algorithm is analytically investigated and tested. The computational results for the proposed algorithm are compared with other Global Search approaches.     

A Self‐Reporting Tetrazole‐Based Linker for the Biofunctionalization of Gold Nanorods

A photochemical approach based on nitrile imine‐mediated tetrazole‐ene cycloaddition is introduced to functionalize gold nanorods with biomolecules. For this purpose, a bifunctional, photoreactive linker containing thioctic acid as the Au anchoring group and a tetrazole moiety for the light‐induced reaction with maleimide‐capped DNA was prepared. The tetrazole‐based reaction on the nanoparticles’ surface results in a fluorescent pyrazoline product allowing for the spectroscopic monitoring of the reaction. This first example of nitrile imine‐mediated tetrazole‐ene cycloaddition (NITEC)‐mediated biofunctionalization of Au nanorods paves the way for the attachment of sensitive biomolecules, such as antibodies and other proteins, under mild conditions and expands the toolbox for the tailoring of nanomaterials.     

SNARE derived peptide mimic inducing membrane fusion

SNARE proteins mediate membrane fusion between synaptic vesicles and the plasma membrane. A minimized peptide SNARE model system with reduced complexity was introduced combining the native SNARE transmembrane (TMD) and linker domains with artificial coiled-coil forming peptides. Specific membrane fusion initiated by coiled-coil recognition was shown by lipid and content mixing vesicle assays.     

Composition and antimicrobial activity of Achillea distans essential oil

The essential oil of Achillea distans W. et K. flower heads was analyzed by GC and GC-MS. Altogether 43 components in concentrations more than 0.1% were identified representing 93.5% of the oil composition. The main constituents were 1,8-cineole (16.8%), trans-thujone (9.8%), sabinene (8.2%), borneol (7.5%), beta-pinene (6.5%), and camphor (5.8%). The oil showed moderate activity against Staphylococcus aureus and Candida albicans, and weak activity against Salmonella typhimurium, Proteus vulgaris, and Escherichia coli.     

Water vapor line shifts in the range 5000–5600 cm<Superscript>−1</Superscript> induced by the pressure of different buffer gases

The coefficients of the water vapor line shifts induced by the pressure of oxygen, nitrogen, and argon are measured and calculated in the spectral range from 5000 to 5600 cm^?1. The experimental data are obtained from the analysis of the absorption spectra of H₂O-O₂, H₂O-N₂, and H₂O-Ar mixtures measured on a Fourier spectrometer with a resolution of 0.007 cm^?1 in a wide pressure range of buffer gases at room temperature for an optical path length of 84.05 m. The calculations are performed according to the Anderson impact theory of broadening with the use of only one adjustable parameter—the effective mean dipole polarizability of the upper vibrational state. The shifts of one and the same lines induced by the pressure of different buffer gases are compared; the role played by different terms of the intermolecular potential in the formation of the shifts is analyzed.