Simultaneous extraction of tocotrienols and tocopherols from cereals using pressurized liquid extraction prior to LC determination

Tocopherols and tocotrienols have been simultaneously determined in food samples using a rapid and simple analytical method including pressurized liquid extraction (PLE) and LC with electrochemical detection. Separation was carried out on a Phenomenex Synergi 4 μm Hydro‐RP 80A column, using a solution of 2.5 mM acetic acid/sodium acetate in methanol/water (99:1, v/v) as mobile phase at a flow rate of 1.0 mL/min. Column temperature was maintained at 30°C. Detection was performed by coulometric detection at 500 mV except for (β+γ)‐tocotrienol, in wheat and rye samples, which was at +350 mV. A palm oil containing a relatively large amount of γ‐tocotrienol and lower concentrations of α‐ and δ‐tocotrienols and α‐ and γ‐tocopherols was used to provide reference retention times for the tocotrienols. Analyte quantification was performed using the external standard method. The calibration equations of tocopherols were used to quantify both tocopherols and their corresponding tocotrienols. The extraction recoveries obtained using the optimized PLE conditions were in the 80–114% range, with RSDs lower than 15%. The method was successfully applied to the determination of tocotrienols and tocopherols in cereal (wheat, rye, barley, maize and oat) and palm oil samples.     

Quasi-classical trajectory calculations analyzing the role of bending mode excitations of methane in the Cl + CH4 reaction

The effects of the methane torsional (nu(2)), umbrella (nu(4)), and the combination nu(2)+nu(4) bending mode excitations on the reactivity and dynamics of the gas-phase Cl + CH(4) --> HCl + CH(3) reaction were analyzed. Quasi-classical trajectory (QCT) calculations, including corrections to avoid zero-point energy leakage along the trajectories, were used on an analytical potential energy surface previously developed by our group. With respect to the reactivity, we found that excitation of either bending mode independently gave similar increases in the reactivity, while the increase observed upon excitation of both modes was larger than the sum of the effect of exciting them independently. Both results agree with recent experimental measures. With respect to the dynamics (rotovibrational and angular distributions of the products), the two bending modes and their combination gave very similar pictures, reproducing the experimental behavior. The satisfactory agreement obtained with a great variety of experimental data (always qualitatively acceptable and sometimes even quantitatively) of the present QCT study lends confidence to the potential energy surface constructed by our group.     

Conidial pigmentation is important to tolerance against solar-simulated radiation in the entomopathogenic fungus Metarhizium anisopliae

The importance of conidial pigmentation to solar UV radiation tolerance in the entomopathogenic fungus Metarhizium anisopliae var. anisopliae, was estimated by comparing the effects of exposure to simulated solar UV radiation on the wild-type parent strain U.S. Department of Agriculture (USDA)-Agricultural Research Service (ARS) Collection of Entomopathogenic Fungal Cultures (ARSEF) 23, which has dark green conidia, and three groups of color mutants with yellow, purple and white conidia. The comparisons included inactivation levels and the kinetics of germination of conidia exposed or not exposed to simulated solar UV radiation. In addition to significantly inactivating the conidia of different mutants, exposure to radiation delayed for several hours the germination of surviving conidia of the wild type and all mutants. In general, mutants with white conidia were more sensitive to simulated solar UV radiation than mutants with purple conidia, which were more sensitive than mutants with yellow conidia, which in turn were more sensitive than the green wild strain. A significant variation in tolerance to simulated solar radiation was observed among mutants within each color group, particularly among mutants with yellow conidia. Revertants with green conidia, DWR 179 and DWR 176, were obtained from the very sensitive UV mutants DWR 148 (yellow conidia) and DWR 149 (purple conidia), respectively. These revertants had levels of tolerance to simulated solar UV radiation similar to those of the wild-type ARSEF 23. This observation is strong evidence of the importance of green conidial pigmentation for tolerance to simulated solar UV radiation, a factor that could be manipulated to produce M. anisopliae strains with more tolerance to solar UV radiation.     

New lipophilic 3-hydroxy-4-pyridinonate iron(III) complexes: synthesis and EXAFS structural characterisation

New tris-iron(III) chelates of 3-hydroxy-4-pyridinone ligands derived from maltol (3-hydroxy-2-methyl-4-pyrone) or ethylmaltol (2-ethyl-3-hydroxy-4-pyrone), including a variety of N-aryl (phenyl, 4'-tolyl, 4'-(n-butyl)phenyl, 4'-(n-hexyl)phenyl) and N-benzyl (4'-methylbenzyl, 4'-fluorobenzyl and 4'-(trifluoromethyl)benzylamine) substituents on the nitrogen atom of the pyridinone ring, have been prepared. Characterization by C,H,N elemental analysis and thermogravimetric measurements indicates that most of the complexes are obtained as hydrates of general formula ML3.xH2O. Structural characterization of these difficult to crystallize lipophilic complexes has been achieved by EXAFS spectroscopy. Solutions of iron(III) complexes of maltol, ethylmaltol, 1,2-dimethyl-3-hydroxy-4-pyridinone and 1-phenyl-2-methyl-3-hydroxy-4-pyridinone in methanol-water mixtures were also examined by EXAFS. Distances from the central atom to ligand atoms, within 6 A of the metal, have been determined in the solid and solution samples and the results show that the structure observed in the powder is maintained in solution. The local structure around the metal centre, bond distances and bond angles, does not change significantly with variable lipophilicity, thus indicating that ligands may be tailored according to specific needs without altering their chelation properties. EXAFS data analysis for this set of tris-iron(III) compounds illustrates the important contribution of both intra-ligand and inter-ligand multiple scattering pathways through the metal centre to a peak observed in the FT spectrum at twice the metal ligand distance (approximately 4 A). The present results demonstrate that EXAFS features at twice the metal-ligand distance are valuable in the assignment of molecular geometry and that location of hydration water molecules, by EXAFS analysis, is limited by the geometry of the complexes, in particular for those in which ligands containing phenyl rings are present.     

Prediction of near field overpressure from quarry blasting

This paper investigates the propagation of airblast or pressure waves in air produced by bench blasting (i.e. detonation of the explosive in a row of blastholes, breaking the burden of rock towards the free vertical face of the block). Peak overpressure is calculated as a function of blasting parameters (explosive mass per delay and velocity at which the detonation sequence proceeds along the bench) and the polar coordinates of the position of interest (distance to the source and azimuth with respect to the free face). The model has been fitted to empirical data using linear least squares. The data set is composed of 122 airblast records monitored at distances less than 400 m in 41 production blasts carried out in two quarries. The model is statistically significant and has a determination coefficient of 0.87. The formula is validated from 12 airblast measurements gathered in five additional blasts.     

Identification of iridoid and sesquiterpenes from <Emphasis Type="Italic">Buddleia parviflora</Emphasis> by NMR spectra

A new compound was elucidated as 9-acetyl-6-caryophyllen-15-ol. Iridoid glucosides including catalpol, methyl catalpol, 7-deoxy-8-epiloganic acid, and aucubin, were isolated from leaves of Buddleia parviflora, while the known compounds were identified as dehydrobuddledin A and buddledin C. The structures was elucidated by extensive 1D-2D-NMR spectroscopy. Published in Khimiya Prirodnykh Soedinenii, No. 1, pp. 29–31, January–February, 2008.     

Efficient numerical analysis of optical imaging data: A comparative study

The computational efficiency of 14 optical detectors over six types of transformations, namely: blur, illumination, rotation, viewpoint, zoom, and zoom-rotation changes, was analyzed. Images with the same resolution (750 × 500 pixels) were studied, in terms of correspondences, repeatability and computing time, and the correspondence was measured by using homographies i.e. projective transformations, to obtain the best efficiency for imaging applications. Results show that the multi-scale Harris Hessian detector is the most efficient for blur, illumination, and zoom-rotation changes. Meanwhile, multi-scale Hessian and Hessian Laplace are the best methods for rotation, viewpoint, and zoom changes.     

Incorporation of stable organic radicals of the tris(2,4, 6-trichlorophenyl)methyl radical series to pyrrole units as models for semiconducting polymers with high spin multiplicity. 1

The condensation reactions between (4-amino-2,6-dichlorophenyl)bis(2, 4,6-trichlorophenyl)methyl radical and acetylacetone or 1, 4-bis(5-methyl-2-thienyl)-1,4-butanedione yield [2,6-dichloro-4-(2, 5-dimethyl-1-pyrrolyl)phenyl]bis(2,4,6-trichlorophenyl)methyl radical (3(*)()) and [2,6-dichloro-4-[2, 5-bis(5-methyl-2-thienyl)-1-pyrrolyl]phenyl]bis(2,4, 6-trichlorophenyl)methyl radical (4(*)()), respectively. EPR studies of both radicals 3(*)() and 4(*)() in CH(2)Cl(2) solution suggest a weak electron delocalization with coupling constant values of 1.25 and 1.30 G, respectively, with the six aromatic hydrogens. Their electrochemical behavior was analyzed by cyclic voltammetry. Both radicals show reversible reduction processes at E degrees = -0.69 V and -0.61 V versus SSCE, respectively, and anodic peak potentials at E(p)(a) = 1.10 and 0.72 V, respectively, versus SSCE at a scan rate (nu) of 200 mV s(-)(1), being reversible for radical 4(*)(). X-ray analysis of radical 3(*)() shows a high value (65 degrees ) of the dihedral angle between the 2,5-dimethylpyrrolidyl moiety and the phenyl ring. Smooth oxidation of radical 4(*)() in CH(2)Cl(2) containing trifluoroacetic acid gives an ionic diradical species with a weak electron interaction (|D/hc| = 0.0047 cm(-)(1)). A Curie plot of the Deltam(s)() = +/-2 signal intensity versus the inverse of the absolute temperature in the range between 4 and 70 K suggests a triplet or a nearly degenerate singlet-triplet ground state.     

Heat capacity and thermodynamic functions of CsCrCl3 and RbCrCl3. Structural phase transitions

We present the heat capacities measured by adiabatic calorimetry from 6 to 350 K, and by differential scanning calorimetry from 300 to 500 K, of CsCrCl₃ and RbCrCl₃. A first-order transition at T_c = (171.1±0.1) K was detected for CsCrCl₃. The RbCrCl₃ showed at T_c = (193.3±0.1) K a transition with thermal hysteresis at temperatures just below the maximum. At T₁ = (440±10) K a continuous transition was also detected. Furthermore, at T_N ≈ 16 K, and for both compounds, a small bump due to magnetic long-range ordering was observed. The thermodynamic functions at 298.15 K are

     

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	$\text{C}{}_{\mathrm{<mtext>p,</mtext><mtext>m</mtext>}}\text{R}$	$\text{S}{}_{\mathrm{m}}{}^{\mathrm{o}}\text{R}$	$\text{{H}{}_{\mathrm{m}}{}^{\mathrm{o}}\text{(T)?H}{}_{\mathrm{m}}{}^{\mathrm{o}}\text{(0)}}\text{R}\text{K}$	$\text{?{G}{}_{\mathrm{m}}{}^{\mathrm{o}}\text{(T)?H}{}_{\mathrm{m}}{}^{\mathrm{o}}\text{(0}}\text{RT}$
CsCrCl3	15.38	26.49	3503.2	14.735
RbCrCl3	15.76	25.99	3556.8	14.384