Mono(pyridine-N-oxide) analog of DOTA as a suitable organic reagent for a sensitive and selective fluorimetric determination of Ln(III) ions

The mono(pyridine-N-oxide) analog of the H₄dota macrocylic ligand, H₃do3a-py^NO, is capable of forming thermodynamically stable and kinetically inert Ln(III) complexes. Its Eu(III) and Tb(III) complexes display a strong long-lived fluorescence as a result of the antenna effect of the pyridine-N-oxide fluorophore in the reagent. It is shown that H₃do3a-py^NO can be used as a fluorogenic reagent for the determination of Eu(III) and Tb(III) at pH 6.5 and c_L=1 mM. At an excitation wavelength of 286 nm, the emission maxima are 615 nm (Eu(III)-complex), and 547 nm (Tb(III)complex). Detection limits are at concentrations around 1.0 μM and linearity of the method spans over 2 orders of magnitude. The method was applied to artificial and real samples (spiked mineral waters, extracts from cathode ray tube luminophore dust) and gave satisfactory results. The method is simple, rapid, and hardly interfered by other metal ions.     

Radical polymerization of 1‐alkenes catalyzed by lithium salts of carboranes

Radical polymerization of selected 1‐alkenes, (1‐hexene, 1‐octene and 2‐methyl‐1‐heptene), initiated with classical radical initiators and catalyzed by lithium salts of selected carboranes was studied. In accordance with recently published results it was found that the use of radical initiators under catalysis by “naked” lithium cation of carboranes promotes the radical polymerization of 1‐alkenes, otherwise nonpolymerizable by the radical mechanism. However, although in our experiments relatively high monomers conversions are reached for some of the thermal initiators used, only low‐molecular‐weight oligomers with M_n < 1000 are formed, regardless of the initiator and carborane anion used. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

TiCl4 and Grignard reagent-promoted ring-opening reactions of various epoxides: synthesis of γ-hydroxy-α,α-difluoromethylenephosphonates

A straightforward methodology for the synthesis of diethyl γ-hydroxy-α,α-difluoromethylenephosphonates is reported. In the presence of titanium tetrachloride, epoxide ring-opening reactions occurred upon treatment with lithium diethyl difluoromethylenephosphonate. When diethyl 3,4-epoxy-1,1-difluorobutylphosphonate was reacted with TiCl₄ and Grignard reagents, the corresponding halohydrins were obtained in very good yields.     

Curing kinetics study of melamine–urea–formaldehyde resin

The influence of the preconditioning at different temperatures on the cure kinetics of melamine?Curea?Cformaldehyde resins coated on stone wool was investigated under acidic conditions using differential scanning calorimetry and thermogravimetry. The higher pre-treatment temperature was applied, to which resin-coated stone wool was exposed, the lower was the mass loss during the experiment. Kinetic model parameters were determined in two different manners, with the parameters being independent of preconditioning temperature and dependent on the latter. The apparent orders of reaction were approximately two (all of them being within the range 0.96?C2.33), which would imply that cross-linking predominantly proceeds via the bimolecular reaction of either melamine or urea and formaldehyde. Nonetheless, the apparent orders of reaction decreased as a function of preconditioning temperature. The apparent activation energies varied less with preconditioning temperature, assuming values between 64.2 and 78.5?kJ?mol^?1. The applicability of nth-order reaction kinetic models was consequently validated for two other dynamic thermal regimes.     

Particle sorting using a porous membrane in a microfluidic device

Porous membranes have been fabricated based on the development of the perforated membrane mold [Y. Luo and R. N. Zare, Lab Chip, 2008, 8, 1688-1694] to create a single filter that contains multiple pore sizes ranging from 6.4 to 16.6 μm inside a monolithic three-dimensional poly(dimethylsiloxane) microfluidic structure. By overlapping two filters we are able to achieve smaller pore size openings (2.5 to 3.3 μm). This filter operates without any detectable irreversible clogging, which is achieved using a cross-flow placed in front of each filtration section. The utility of a particle-sorting device that contains this filter is demonstrated by separating polystyrene beads of different diameters with an efficiency greater than 99.9%. Additionally, we demonstrate the effectiveness of this particle-sorting device by separating whole blood samples into white blood cells and red blood cells with platelets.     

Meson production inp+U,O+U and S+U interactions at 200 GeV/nucleon

Meson production in proton, oxygen and sulphur interactions with uranium targets at 200 GeV/nucleon is studied. We measure the inclusive meson cross-section d /dP _T ² and its evolution fromp+U to S+U. The cross-section fitted with an exponential gives an inverse slopeP _T0 of the order of 210 MeV/c. As a function of the neutral transverse energy,P _T0 values show a slight rise followed by a plateau. The normalized difference (⁺–^–)/^– between positive and negative meson cross-sections is found to increase withE _T .also at ISEL     

Advanced chiral molecular media for enantioselective electrochemistry and electroanalysis

An increasing number of strategies and tools have been proposed to endow the electrochemical interphase with chirality, to achieve enantiodiscrimination in analytical and/or preparative applications. So far, chirality has mostly been implemented not only at the electrode surface side but also on the medium one. Recently, the attractiveness of the latter approach has remarkably increased on account of the increasing availability of advanced chiral molecular media with intrinsic attractive features for electrochemistry applications, such as chiral ionic liquids, chiral ionic liquid crystals, and chiral deep eutectic solvents. With respect to solid layer/fixed chiral networks, advanced chiral media can still offer a reasonably high degree of local structuring, while being less demanding concerning preparation and management protocols, as well as less sensitive to fouling/regeneration issues. Different ways to implement chirality in advanced molecular media, including cases of powerful ‘inherent chirality,’ will be presented and discussed, particularly focusing on recent applications in the electrochemical field.     

Simple synthesis of some unsaturated 1,1-difluoro-2-hydroxyethylphosphonates

A short synthesis of some 1,1-difluoro-2-hydroxymethylphosphonates in good yields is described. This procedure involves the regioselective 1,2-addition of [(diethoxyphosphoryl)difluoromethyl]lithium toward unsaturated aldehydes and ketones.     

Open beauty production in high energy π−-tungsten interactions

We present a study of \(B\bar B\) meson pair production inπ ^? interactions at 140, 194 and 286 GeV incident pion energy. At 286 GeV, where we have the best statistics, we find a model-dependent \(B\bar B\) production cross-section \(\sigma _{BB} = 14_{ - 6}^{ + 7} nb/nucleon\) .     

Enantioselective selectors for chiral electrochemistry and electroanalysis: Stereogenic elements and enantioselection performance

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