Search for anomalous production of multilepton events in pp collisions at sqrt s=1.96 TeV

We report a search for the anomalous production of events with multiple charged leptons in pp[over] collisions at sqrt[s]=1.96 TeV using a data sample corresponding to an integrated luminosity of 346 pb(-1) collected by the CDF II detector at the Fermilab Tevatron. The search is divided into three-lepton and four-or-more-lepton data samples. We observe six events in the three-lepton sample and zero events in the > or =4-lepton sample. Both numbers of events are consistent with standard model background expectations. Within the framework of an R-parity-violating supergravity model, the results are interpreted as mass limits on the lightest neutralino (chi[over](1)(0)) and chargino (chi[over](1+/-) particles. For one particular choice of model parameters, the limits are M(chi[over](1)(0)>110 GeV/c2 and M(chi[over](1+/-)>203 GeV/c2 at 95% confidence level; the variation of these mass limits with model parameters is presented.     

Atomic dimer shuttling and two-level conductance fluctuations in Nb nanowires

We present high-resolution conductance measurements in niobium nanowires below the superconducting transition temperature. During elongation we find a bistability region manifesting itself as random telegraph noise. Density functional structural optimizations and conductance calculations reproduce and explain the measurements. In particular, the observed bistability is associated with the formation of a niobium dimer between the opposing electrodes, with the dimer shuttling between a symmetric, high conductance, and an asymmetric, low-conductance configurations in the gap.     

Evaluation of tris(4,7-diphenyl-1,10-phenanthrolinedisulfonate)ruthenium(II) as a chemiluminescence reagent

Previous studies have suggested that tris(4,7-diphenyl-1,10-phenanthrolinedisulfonate)ruthenium(II) (Ru(BPS)₃⁴⁻) has great potential as a chemiluminescence reagent in acidic aqueous solution. We have evaluated four different samples of this reagent (two commercially available and two synthesised in our laboratory) in comparison with tris(2,2′-bipyridine)ruthenium(II) (Ru(bipy)₃²⁺) and tris(1,10-phenanthroline)ruthenium(II) (Ru(phen)₃²⁺), using a range of structurally diverse analytes. In general, Ru(BPS)₃⁴⁻ produced more intense chemiluminescence, but the oxidised Ru(BPS)₃³⁻ species is less stable in aqueous solution than Ru(bipy)₃³⁺ and produced a greater blank signal than Ru(bipy)₃³⁺ or Ru(phen)₃³⁺, which had a detrimental effect on sensitivity. Although the complex is often depicted with the sulfonate groups of the BPS ligand in the para position on the phenyl rings, NMR characterisation revealed that the commercially available BPS material used in this study was predominantly the meta isomer.     

Polymeric and polymer-ligated spirobicyclic zwitterionic Janovsky complexes

A novel approach to the synthesis of spirobicyclic Janovsky complexes is described. The complexes were prepared on silica and polystyrene polymeric supports as well as on a solution-borne poly(carbodiimide) polymer with 100% atom economy. A carbon-centered intramolecular de-aromatizing nucleophilic aromatic substitution ipso-cyclization mechanism describes the synthesis of these spirobicyclics. The molecules were characterized by solution and solid-state ¹H and ¹³C NMR, IR, and MS.     

Preliminary evaluation of monolithic column high-performance liquid chromatography with tris(2,2′-bipyridyl)ruthenium(II) chemiluminescence detection for the determination of quetiapine in human body fluids

High-performance liquid chromatography (HPLC) with tris(2,2′-bipyridyl)ruthenium(II) chemiluminescence detection methodology is reported for the determination of the atypical antipsychotic drug quetiapine and the observation of its major active and inactive metabolites in human urine and serum. The method uses a monolithic chromatographic column allowing high flow rates of 3 mL min⁻¹ enabling rapid quantification. Flow injection analysis (FIA) with tris(2,2′-bipyridyl)ruthenium(II) chemiluminescence detection and HPLC time of flight mass spectrometry (TOF-MS) were used for the determination of quetiapine in a pharmaceutical preparation to establish its suitability as a calibration standard. The limit of detection achieved with FIA was 2 × 10⁻¹¹ mol L⁻¹ in simple aqueous solution. The limits of detection achieved with HPLC were 7 × 10⁻⁸ and 2 × 10⁻¹⁰ mol L⁻¹ in urine and serum, respectively. The calibration range for FIA was between 5 × 10⁻⁹ and 1 × 10⁻⁶ mol L⁻¹. The calibration ranges for HPLC were between 1 × 10⁻⁷-1 × 10⁻⁴ and 1 × 10⁻⁸-1 × 10⁻⁴ mol L⁻¹ in urine and serum, respectively. The quetiapine concentrations in patient samples were found to be 3 × 10⁻⁶ mol L⁻¹ in urine and 7 × 10⁻⁷ mol L⁻¹ in serum. Without the need for preconcentration, the HPLC detection limits compared favourably with those in previously published methodologies. The metabolites were identified using HPLC-TOF-MS.     

Protein fractionation and detection for metalloproteomics: challenges and approaches

At least one third of all proteins are thought to require a metal ion co-factor for their function. Recognition of the importance of metals in biological systems and major advances in analytical instrumentation and technology have led to the emergence of the new research area of metalloproteomics in recent years. Despite this progress, the experimental determination of in-vivo metal cofactors has remained challenging, because this requires elucidation of protein interactions with non-covalently bound metal ions. This critical review highlights current methodological approaches, focusing, in particular, on issues relating to the fractionation and separation of the metalloproteome, including recent experience with metalloproteomics for marine cyanobacteria in our laboratory. Metalloproteomics promises to deliver novel insights into fundamental biological processes in the future, but it is clear that further methodological advances are necessary to exploit the full potential of this emerging research area.     

Productive and ineffective efforts: how student effort in high school mathematics relates to college calculus success

Relativizing the popular belief that student effort is the key to success, this article finds that effort in the most advanced mathematics course in US high schools is not consistently associated with college calculus performance. We distinguish two types of student effort: productive and ineffective efforts. Whereas the former carries the commonly expected benefits, the latter is associated with negative consequences. Time spent reading the course text in US high schools was negatively related to college calculus performance. Daily study time, however, was found to be either a productive or an ineffective effort, depending on the level of high school mathematics course and the student's performance in it.     

Greatest common divisors from generalized sylvester resultant matrices

Sylvester's classical resultant matrix for determining the degree of the greatest common divisor of two polynomials has recently been generalized to deal with m+1 polynomialsm>1. A slightly stronger version is given in this paper for the case when the polynomials do not all have the same degree. The proof relies .on using an appropriate companion matrix, and thereby provides a link with previous work using this approach. It is then shown how the coefficients in a greatest common divisor can be obtained by reducing this extended resultant matrix to row echelon form, this again being an extension of a previous result for the casem=1. Finally, it is shown how the results can be modified when the polynomials are expressed relative to an arbitrary orthogonal basis.