Synthesis of the methanesulfonates of α-(4-chlorophenyl)-α-[1-(2-chlorophenyl)emenyl]-1H-1,2,4-triazole-1-ethanol and α-[1-(2-chlorophenyl)ethenyl]-α-(2,4-difluorophenyl)-1H-1,2,4-triazole-1-ethanol,alpha styryl carbinol antifungal agents

The methanesulfonates of (α-(4-chlorophenyl)-α-[1-(2-chlorophenyl)ethenyl]-1H-1,2,4-triazole-1-ethanol and α-[1-(2-chlorophenyl)ethenyl]-α-(2,4-difluorophenyl)-1H-1,2,4-triazole-1-ethanol ( 1a, b ) are orally effective α-styryl carbinol derivatives developed for the treatment and prevention of systemic fungal infections. Practical new processes amenable for the large-scale production of these compounds are described. Of note is the selection of dichlorostyrene as a convenient precursor of the styryl portion, modification of a sensitive Grignard addition into a realistic preparative reaction and the use of 1,2,4-triazole simultaneously as a base transfer agent and nucleophile.     

Non-aqueous electrolytes for isotachophoresis of weak bases and its application to the comprehensive preconcentration of the 20 proteinogenic amino acids in column-coupling ITP/CE–MS

Isotachophoresis (ITP) has long been used alone but also as a preconcentration technique for capillary electrophoresis (CE). Unfortunately, up to now, its application is restricted to relatively strong acids and bases as either the degree of (de)protonation is too low or the water dissociation is too high, evoking zone electrophoresis. With the comprehensive ITP analysis of all 20 proteinogenic amino acids as model analytes, we, here, show that non–aqueous ITP using dimethylsulfoxide as a solvent solves this ITP shortcoming. Dimethylsulfoxide changes the pH regime of analytes and electrolytes but, more importantly, strongly reduces the proton mobility by prohibiting hydrogen bonds and thus, the so-called Zundel–Eigen–Zundel electrical conduction mechanism of flipping hydrogen bonds. The effects are demonstrated in an electrolyte system with taurine or H⁺ as terminator, and imidazole as leader together with strong acids such as oxalic and even trifluoroacetic acid as counterions, both impossible to use in aqueous solution. Mass spectrometric as well as capacitively coupled contactless conductivity detection (C⁴D) are used to follow the ITP processes. To demonstrate the preconcentration capabilities of ITP in a two-dimensional set-up, we, here, also demonstrate that our non-aqueous ITP method can be combined with capillary electrophoresis–mass spectrometry in a column-coupling system using a hybrid approach of capillaries coupled to a microfluidic interface. For this, C⁴D was optimized for on-chip detection with the electrodes aligned on top of a thin glass lid of the microfluidic chip.     

Polymer-coated cation exchangers in high-performance ion chromatography: preparation and application

Low-capacity cation-exchange stationary phases for ion chromatography were prepared by coating a vinyl-modified silica gel with polystyrene or poly(glycidyl methacrylate). Strong acid ion-exchange groups were formed by sulphonation with concentrated sulphuric acid or by ring opening of the polymer-coated silica gels with sulphite solution. Carbon-sulphur elemental analyses of the polymer-coated cation exchangers (PCCEs) were applied to determine the average polymer film thickness. The pH stability depended on the polymer film thickness. The PCCEs were stable in the pH range 0.5–9. The low-capacity PCCEs (capacities 18–91 μmol/g) were applied to determine alkali and alkaline earth metal ions in tap and mineral waters.     

New attempt to determine the n-n scattering length with the 2H(n, np)n reaction

The n-n final-state interaction (FSI) was investigated via the 2H(n, np)n reaction at 25 MeV, using a geometry which enables the simultaneous observation of n-p quasifree (QFS) scattering. The data were analyzed with Monte Carlo simulations based on rigorous Faddeev calculations with realistic nucleon-nucleon potentials. The value of a(nn) deduced from the absolute yield in the FSI peak is -16.27+/-0. 40 fm while the relative data, normalized in the QFS region, give -16.06+/-0.35 fm. Thus our results differ from the "recommended" value of a(nn) = -18.5+/-0.3 fm by more than 5 standard deviations.     

Double cascade turbulence and Richardson dispersion in a horizontal fluid flow induced by Faraday waves

We report the experimental observation of Richardson dispersion and a double cascade in a thin horizontal fluid flow induced by Faraday waves. The energy spectra and the mean spectral energy flux obtained from particle image velocimetry data suggest an inverse energy cascade with Kolmogorov type scaling E(k) ∝ k(γ), γ ≈ -5/3 and an E(k) ∝ k(γ), γ ≈ -3 enstrophy cascade. Particle transport is studied analyzing absolute and relative dispersion as well as the finite size Lyapunov exponent (FSLE) via the direct tracking of real particles and numerical advection of virtual particles. Richardson dispersion with <ΔR(2)(t)> ∝ t(3) is observed and is also reflected in the slopes of the FSLE (Λ ∝ ΔR(-2/3)) for virtual and real particles.     

Inverse colloidal crystal membranes for hydrophobic interaction membrane chromatography

A collaborative study on the robustness and portability of a capillary electrophoresis‐mass spectrometry method for peptide mapping was performed by an international team, consisting of 13 independent laboratories from academia and industry. All participants used the same batch of samples, reagents and coated capillaries to run their assays, whereas they utilized the capillary electrophoresis‐mass spectrometry equipment available in their laboratories. The equipment used varied in model, type and instrument manufacturer. Furthermore, different types of sheath‐flow capillary electrophoresis–mass spectrometry interfaces were used. Migration time, peak height and peak area of ten representative target peptides of trypsin‐digested bovine serum albumin were determined by every laboratory on two consecutive days. The data were critically evaluated to identify outliers and final values for means, repeatability (precision within a laboratory) and reproducibility (precision between laboratories) were established. For relative migration time the repeatability was between 0.05 and 0.18% RSD and the reproducibility between 0.14 and 1.3% RSD. For relative peak area repeatability and reproducibility values obtained were 3–12 and 9–29% RSD, respectively. These results demonstrate that capillary electrophoresis‐mass spectrometry is robust enough to allow a method transfer across multiple laboratories and should promote a more widespread use of peptide mapping and other capillary electrophoresis‐mass spectrometry applications in biopharmaceutical analysis and related fields.     

Determination of polyamines in biological materials by HPLC with 9-fluorenylmethyl chloroformate precolumn derivatization

Di- and polyamines have been determined in the femtomol range by liquid chromatography on a reversed-phase C₈ column with a linear gradient of acetate buffer/acetonitrile as mobile phase and fluorimetric detection at 265/310 nm after simple derivatization with 9-fluorenylmethyl chloroformate (FMOC) within 3 min at pH 7.8 in presence of aspartic acid to remove excess reagent. The FMOC—polyamine-derivatives have been stable in a methanol—water-solution for at least 10 h. The method can be directly applied to crude plant extracts, and it is not interfered by carbohydrates and phenolics.     

Thermal decomposition of azoisopropane. II. Secondary decomposition processes

The thermal decomposition of azoisopropane (AIP) was studied in the presence of various quantities of propylene in the temperature and pressure intervals 498–553 K and 3.33–5.33 kPa. The inhibition functions relating to formation of the products were determined; these proved a good basis for interpretation of the formation of the secondary decompositon products of AIP. The experimental data support the conception that the βμ radical—radical reaction occurs. The product of this is not stable; its decomposition is one of the sources of the secondary products. The ratio of the rate constants was determined for the following reactions: