Comparison of inductively coupled plasma mass spectrometry techniques in the determination of platinum in urine: quadrupole vs. sector field

In recent years the increasing use of platinum (Pt) both in medical and in industrial applications has caused its growing anthropogenic emission and spread in the environment. Pt is released into the atmosphere by exhaust catalytic converters, and Pt compounds are often used in antitumour therapies. As a consequence, significant amounts of Pt can be detected in hospital wastewaters. This can lead to an increase in the exposure levels to Pt, especially in urban areas. It is therefore necessary to determine Pt reference values in the general population, by using suitable procedures able to achieve adequate analytical performances. Several measurements of Pt in biological fluids have been reported, but the analytical methods used for the determination of Pt often lack information about the uncertainty of the results, especially for low concentrations of urinary Pt in non-occupationally exposed subjects. The present paper considers the measurement of urinary Pt levels in a general population group from central Italy, by both quadrupole (Q) and sector field (SF) inductively coupled plasma mass spectrometry (ICP-MS). The two procedures were validated and their expanded uncertainties were evaluated. The limits of detection (LODs), calculated taking into account dilution factors, were 0.18 and 0.05 ng L(-1) of Pt for the Q and SF procedures, respectively. The median value observed was 4.13 ng L(-1) of Pt in urine, while the relative combined uncertainty at 5 ng L(-1) was below 20% with both ICP-MS techniques. These data are in good agreement with those reported in the literature for similar studies.     

Different lethal effects by enzyme-generated triplet indole-3-aldehyde in different Escherichia coli strains

Strains of Escherichia coli which lack 4-thiouridine (S4U) exhibit a higher survival rate than their wild-type parents which contain S4U after treatment with enzyme-generated triplet indole-3-aldehyde. In a similar manner to results obtained with monochromatic 334 nm UV light, the survival is related to single-strand breakage of DNA in E. coli containing the pBR 322 plasmid. The effects of the excited states generated by an enzymatic system suggest that S4U is an important chromophore in the lethal effects observed. The results also suggest that the energy transferred from triplet indole-3-aldehyde to S4U may also be passed from S4U of t-RNA to DNA, possibly through a singlet oxygen intermediate generated by excited S4U, resulting in a decrease in the survival rate of E. coli containing S4U. These results emphasize the importance of excited states in biological systems.     

Quantum imaging and spatio-temporal correlations

We report on recent progress for two topics in the field of Quantum Imaging. The first is the detection of faint amplitude objects with a sensitivity which surpasses the standard quantum limit. The second is the theoretical/numerical analysis of spatio-temporal entanglement in optical parametric down-conversion.     

Noiseless amplification of images in a confocal cavity

We study the noiseless amplification of an optical image by means of a confocal cavity containing a parametric medium. We demonstrate, in the ideal situation, the possibility of preserving the signal-to-noise ratio while amplifying uniformly the entire image. Some specific effects, which may degrade the performances of the scheme, are taken into account. Received 23 March 2000     

Insights on spin polarization through the spin density source function

Understanding how spin information is transmitted from paramagnetic to non-magnetic centers is crucial in advanced materials research and calls for novel interpretive tools. Herein, we show that the spin density at a point may be seen as determined by a local source function for such density, operating at all other points of space. Integration of the local source over Bader''s quantum atoms measures their contribution in determining the spin polarization at any system''s location. Each contribution may be then conveniently decomposed in a magnetic term due to the magnetic natural orbital(s) density and in a reaction or relaxation term due to the remaining orbitals density. A simple test case, ³B₁ water, is chosen to exemplify whether an atom or group of atoms concur or oppose the paramagnetic center in determining a given local spin polarization. Discriminating magnetic from reaction or relaxation contributions to such behaviour strongly enhances chemical insight, though care needs to be paid to the large sensitivity of the latter contributions to the level of the computational approach and to the difficulty of singling out the magnetic orbitals in the case of highly correlated systems. Comparison of source function atomic contributions to the spin density with those reconstructing the electron density at a system''s position, enlightens how the mechanisms which determine the two densities may in general differ and how diverse may be the role played by each system''s atom in determining each of the two densities. These mechanisms reflect the quite diverse portraits of the electron density and electron spin density Laplacians, hence the different local concentration/dilution of the total and (α–β) electron densities throughout the system. Being defined in terms of an observable, the source function for the spin density is also potentially amenable to experimental determination, as customarily performed for its electron density analogue.     

C2-symmetric chiral disulfoxide ligands in rhodium-catalyzed 1,4-addition: from ligand synthesis to the enantioselection pathway

A family of chiral C(2)-symmetric disulfoxide ligands possessing biaryl atropisomeric backbones has been synthesized by using the Andersen methodology. Complete characterization includes X-ray crystallographic studies of all ligands and some of their rhodium complexes. Their synthesis, optical purity, electronic properties, and catalytic behavior in the prototypical rhodium-catalyzed 1,4-addition of phenylboronic acid to 2-cyclohexen-1-one are presented through an in depth study of this ligand class. Density functional theory calculations on the step of the catalytic cycle that determines the enantioselectivity are presented and reinforce the first hypothetical explanations for the high levels of asymmetric induction observed.     

Passive mode-locking of a diode-pumped Tm:GdLiF4 laser

We propose an optical near-field assisted sputtering method for repairing scratches on the surface of polycrystalline ceramics in a self-assembling manner. An Al₂O₃ source was sputtered on substrates with laser radiation of wavelength 473 nm. The average depth of the scratched grooves on polycrystalline Al₂O₃ ceramic substrate decreased from 3.2 nm to 0.79 nm. Using a Hough transform, we also confirmed the selective repair of scratches.     

2,7-dimethyl-3,8-dinitrodipyrazolo[1,5-a:1',5'-d]pyrazine-4,9-dione: a new labelling reagent for liquid chromatographic analysis of amino acids

Linear alkylbenzenes (LABs) are discharged into the environment as sub-products of linear alkylbenzenesulfonate (LAS) detergent. Their association with LAS is attributed to the incomplete sulfonation of the LABs in detergent manufacturing resulting in products having LAB. Recently there has been widespread interest in their use as markers of sewage effluent in the aquatic environment. Although LABs may be potentially useful in assessing the distribution and degradation of domestic wastewater, studies about it are still limited probably due to the analytical difficulties.In this article, a new analytical method for the determination of LABs in detergents using gas chromatography coupled to mass spectrometry (GC-MS) in combination with solid phase microextraction (SPME) is proposed. This alternative sample preparation technology presents several advantages, since it is solvent free, fast, uses the whole sample for analysis, requires only small amounts of sample and the fibers for the extraction procedure are reusable. A factorial experimental design was utilized to obtain the optimum values for the main operational parameters in the analysis of LABs in detergents using direct SPME in the pre-concentration step.     

Efficient ring-closing metathesis of alkenyl bromides: the importance of protecting the catalyst during the olefin approach

We present the first productive ring-closing metathesis reaction that leads to the construction of cyclic alkenyl bromides. Efficient catalysis employing commercially available Grubbs II catalyst is possible through appropriate modification of the starting bromoalkene moiety.