Simultaneous Determination of Chromium Species in Water and Plant Samples at Trace Levels by Ion Chromatography–Inductively Coupled Plasma-Mass Spectrometry

Ion chromatography–inductively coupled plasma-mass spectrometry (IC–ICP-MS) was used for the identification and quantification of chromium species. Chromium(III) and chromium(VI) were separated and determined by IC–ICP-MS. The separation was achieved using an anion exchange column with 0.55?M HNO₃ as mobile phase. It was a particular goal of this work to exclusively use nitric acid for elution in order to reduce interferences in the ICP-MS system. Analytical figures of merit were calculated under the optimum conditions by developing calibration plots in a concentration range of 0.50–250?µg/L for both species. The detection limits for Cr(III) and Cr(VI) were 0.09 and 0.03?µg/L, respectively. Spiked recovery tests were used to evaluate the applicability of the analytical method in environmental samples, and the recoveries ranged between 97 and 103% for both analytes. The accuracy of the method for total chromium content was validated through the analysis of a spring water-certified reference material (UME 1201), and the obtained results were in good agreement with the certified value. Lettuce seedlings were cultivated to evaluate the intake levels of these species. In addition, the bioaccessibility of Cr(III) and Cr(VI) from the lettuce seedlings in simulated gastric and intestinal fluids media was examined.     

Dynamic Destruction as Analogs of Critical Phenomena in Metal Samples with Various Geometries within a Wide Ranges of Amplitude–Time Characteristics of External Action

Physics of Atomic Nuclei - The quantitative characteristics of the products of dispersion and the cascade of dissipative structures arising in metals under shock-wave loading are determined. The...     

Substantiation of the Possibility of Predicting Behavior of Solids under Extreme Conditions at Various High-Intensity Impacts

The paper is devoted to the data analysis on the amplitude-time regularities of the dynamic failure process of solids under various types of high-intensity impact in the ranges of nonequilibrium states from 3 × 10^?10 to 10^?5 s and establishing general regularities of behavior of unstudied materials under extreme conditions. We have analyzed the process of dynamic destruction of solids of different nature using the method of magnetic-pulse loading in the microsecond range of nonequilibrium states, as well as the dynamic failure process for a number of metals in the mode of pulsed volume heating under the action of pulsed relativistic electron beams in the nanosecond and subnanosecond range of nonequilibrium states. It has been shown that, upon using different methods of pulsed loading in the dynamic longevity range, the failure time as a function of amplitude of applied load has an exponential form for various solid materials. This indicates the scaling nature of the destruction process. The foregoing determines the possibility of predicting the behavior of unstudied solid bodies in the dynamic range of nonequilibrium states.     

Pd‐PEPPSI‐IPent: An Active,Sterically Demanding Cross‐Coupling Catalyst and Its Application in the Synthesis of Tetra‐Ortho‐Substituted Biaryls

Incredible Bulk : A series of N‐heterocyclic carbene catalysts (see picture) were prepared and evaluated in the Suzuki–Miyaura reaction. A variety of sterically encumbered tetra‐ortho‐substituted biaryl products were formed from unreactive aryl chlorides using the isopentyl‐substituted catalyst at temperatures ranging from 65 °C to room temperature. The cyclopentyl‐substituted catalyst was virtually inactive, demonstrating that “flexible bulk” is essential to promote these transformations.

     

The Development of Bulky Palladium NHC Complexes for the Most-Challenging Cross-Coupling Reactions

Palladium‐catalyzed cross‐coupling reactions enable organic chemists to form C? C bonds in targeted positions and under mild conditions. Although phosphine ligands have been intensively researched, in the search for even better cross‐coupling catalysts attention has recently turned to the use of N‐heterocyclic carbene (NHC) ligands, which form a strong bond to the palladium center. PEPPSI (pyridine‐enhanced precatalyst preparation, stabilization, and initiation) palladium precatalysts with bulky NHC ligands have established themselves as successful alternatives to palladium phosphine complexes. This Review shows the success of these species in Suzuki–Miyaura, Negishi, and Stille–Migita cross‐couplings as well as in amination and sulfination reactions.     

The effect of temperature on the nonlinear dynamics of charge in a semiconductor superlattice in the presence of a magnetic field

The space-time dynamics of electron domains in a semiconductor superlattice is studied in a tilted magnetic field with regard to the effect of temperature. It is shown that an increase in temperature substantially changes the space-time dynamics of the system. This leads to a decrease in the frequency and amplitude of oscillations of a current flowing through the semiconductor superlattice. The quenching of oscillations is observed, which is attributed to the change in the drift velocity as a function of electric-field strength under the variation of temperature.     

Amination with Pd-NHC complexes: rate and computational studies involving substituted aniline substrates

The amination of aryl chlorides with various aniline derivatives using the N-heterocyclic carbene-based Pd complexes Pd-PEPPSI-IPr and Pd-PEPPSI-IPent (PEPPSI=pyridine, enhanced precatalyst, preparation, stabilization, and initiation; IPr=diisopropylphenylimidazolium derivative; IPent= diisopentylphenylimidazolium derivative) has been studied. Rate studies have shown a reliance on the aryl chloride to be electron poor, although oxidative addition is not rate limiting. Anilines couple best when they are electron rich, which would seem to discount deprotonation of the intermediate metal ammonium complex as being rate limiting in favour of reductive elimination. In previous studies with secondary amines using PEPPSI complexes, deprotonation was proposed to be the slow step in the cycle. These experimental findings relating to mechanism were corroborated by computation. Pd-PEPPSI-IPr and the more hindered Pd-PEPPSI-IPent catalysts were used to couple deactivated aryl chlorides with electron poor anilines; while the IPr catalysis was sluggish, the IPent catalyst performed extremely well, again showing the high reactivity of this broadly useful catalyst.     

A detailed investigation of the electronic properties of a multi-layer spherical quantum dot with a parabolic confinement

In this work, we aim a detailed investigation of the electronic properties of a spherical multi-layer quantum dot with and without a hydrogenic impurity. The structure is introduced in the form of core/shell/well/shell layers. The core and well layers are defined by the parabolic electronic potentials. We carry out the effect of the core radius and layer thickness on the energy levels, their wave functions, binding energies of the impurity and the probability distributions. In order to determine the sublevel eigenvalues and eigenfunctions, the Schrödinger equation is solved full numerically by shooting method in the frame of the effective mass approximation. The results are analyzed in detail as a function of the layer thicknesses and their probable physical reasons are tried to be explained. It is found that the electronic properties and impurity binding energies are strongly depending on the layer thicknesses.     

Photoreflection and photoconduction spectra of CdS crystals: Excitons in the electric fields of surface states

The exciton photoreflection spectra of CdS crystals are studied. It is found that the form of the exciton photoreflection spectrum is determined by a Stark shift of the exciton energy in the electric field of surface states. The dependences of the exciton photoreflection spectrum on temperature on the intensity and wavelength of the modulating radiation, and on the processes by which the photoreflection signal relaxes is determined. An energy scheme is proposed for the surface states which explains the observed effects of photoinduced changes in the surface field. A correlation is established between the exciton photoreflection spectrum and the form of the fine structure in the photoconductivity. Fiz. Tverd. Tela (St. Petersburg) 40, 875–876 (May 1998)     

On the existence of minimal τ-closed ω-saturated non-$ \mathfrak{H} $-formations

We study minimal τ-closed ω-local non- \mathfrakH \mathfrak{H} -formations in the case where H is a formation of the classic type.