Effects of UV-B radiation on the Patagonian Jaborosa magellanica Brisben

Treatment of Jaborosa magellanica with artificial UV-B radiation caused changes in plant growth, plant chemistry and increase DNA polymorphisms. Spectrophotometric analysis showed that UV-B radiation decreases the chlorophylls content, and increases the amount of UV-B absorbing compounds (e.g., phenylpropanoids). Other UV-induced alterations include reduction in leaf area, alterations in plant architecture, and DNA damage. Using random primers and PCR amplification procedure, a high degree of polymorphism was detected when treated plants were compared to non-irradiated plants. These biochemical changes may be interpreted as plant response to UV-B radiation stress and as an indicator of DNA damage.     

Solid-phase extraction and sample stacking-micellar electrokinetic capillary chromatography for the determination of multiresidues of herbicides and metabolites

Micellar electrokinetic capillary chromatography (MEKC) with diode array detection was used for the separation of 13 compounds (eight herbicides widely used in agriculture: metribuzin, lenacil, ethofumesate, atrazine, terbutryn, isoproturon, chlorotoluron and linuron, and five of their principal degradation products; namely, deethylatrazine, 2-hydroxyatrazine, deethyl-2-hydroxyatrazine, deisopropylatrazine and 3-chloro-4-methylphenylurea). Peak separation for the 13 analytes was not successful when a single surfactant system was employed, neither sodium dodecyl sulfate (SDS) nor dioctyl sulfosuccinate (DOSS) sodium salt. However, a mixture of these herbicides was successfully separated using a mixed micellar system involving SDS–DOSS in less than 14 min. An application study of an on-line concentration technique for MEKC was carried out to enhance sensitivity. The optimized on-line stacking procedure consisted simply of the addition of 50 mM of sodium chloride to the injection sample, the stacking effect being more intensive as analyte polarity increased. When this stacking procedure was combined with an off-line sample preconcentration step, based on solid-phase extraction, analytes could be detected in the ppb range. The whole method was applied to ultra-high-quality and natural waters. Linear relationships between the analytical signal and the initial analyte concentration were found to be independent of the type of water, except for the more polar analytes for which small differences were observed.     

Freie Elektronenpaare in lokalisierten CNDO/2-Wellenfunktionen der Stickstoffverbindungen

The method for constructing hybrid orbitals described earlier is now used for the analysis of CNDO/2 wave functions of molecules containing nitrogen atoms in order to get information on the type of hybridization of nitrogen lone pair orbitals in various compounds.     

Preparation and basic physical properties of BiTeI single crystals

A modified Bridgman method is described, which makes it possible to prepare homogeneous BiTeI crystals using excess iodine. At room temperature the values of the electrical conductivity of the crystals range around 2000 ^–1 cm^–1, the Hall constant value about 0·09 cm^–3 coul^–1, the Seebeck coefficient about 50 V K^–1. In connection with the assumption of super-stoichiometric iodine content we expect there exist point defects in the crystals, where Te atoms are replaced with I atoms, which gives rise to electric conductivity. On the basis of the temperature dependence of the electron mobility one can suppose a mixed mechanism of the scattering of the free carriers by the acoustic branch of lattice vibrations and by ionized impurities.     

Gamma radiation from the209Bi(3He, 3nγ)209at reaction

Gamma-radiation from the reactions of 28 MeV and 26 MeV³He-ions on the²⁰⁹Bi target has been studied by means of Ge(Li) detectors. Individual observed prompt -ray transitions have been assigned to the corresponding reactions. The results of previous studies of the²⁰⁹At nucleus have been verified and completed. Two new levels at energies of 640 keV and 1270·5 keV have been introduced. Additionally, 15 new transitions have been observed which could belong to²⁰⁹At. The²⁰⁹At level structure is discussed in terms of nuclear models.     

Shockley surface states on three faces of bcc iron

Strictly localized or resonance Shockley surface states have been found on the (111), (010) and (110) faces of paramagnetic bcc iron for ,¯M and ¯N points in the corresponding surface Brillouin zones. Energy, character of wave function and its damping for these states are reported. Emphasis is laid on implications of surface states in photoemission, field-electron and -ion emission, electron energy-loss or disappearance potential spectroscopy, Auger electron spectroscopy, work function, magnetic properties, electric conductivity, as well as chemisorption and catalysis.     

Mechanism of hydrogenolysis and isomerization of oxacyloalkanes on metals, V. Selectivities of metal catalysts in ring-opening reactions of oxiranes

The deoxygenation of methyloxirane to propene and its isomerization to oxo compounds on a Ni/SiO₂ catalyst were studied in a pulse microreactor, in the presence of H₂ as carrier gas, at 473 K. It was found that the deoxigenation leads to the creation of new types of active centers (Lewis acid site-basic site), which cause a change in the direction of ring opening. The differences in regioselectivity observed between Ni and Cu, and Pt and Pd, can be explained by the different affinities of the metals for oxygen. This finding can be generalized to other oxygen-containing compounds.

---

=qa Ni/SiO₂ 473 . , - - , . Ni Cu, Pt Pd . .

---

---

Part IV: J. Catal. (to be published)     

A common method for the determination of several calcium channel blockers using an HPLC system with ultraviolet detection

We report a common HPLC method for the single or simultaneous determination of four calcium channel blockers (CCB), namely diltiazem (DTZ), verapamil (VER), nifedipine (NIF) and nitrendipine (NIT) and their active metabolites demetildiltiazem and deacetildiltiazem (MA and M1), norverapamil (NOR), and dehydronifedipine (DHN). DHN was first synthesised in our laboratory and different pH values of the mobil phase were subsequently prepared and tested for chromatographic separation. The detection system and the environmental light conditions were optimised. The best separations of all analytes were obtained using a C₁₈ column and a mobile phase of methanol, 0.04 M ammonium acetate, acetonitrile and triethylamine (2:2:1:0.04 v/v). Quantitation was performed using imipramine (IMI) as the internal standard. For DTZ and its metabolites (M1 and MA), the wavelength chosen was 237 nm; for VER and its metabolite NOR, it was 210 nm; and, finally for NIF and its metabolite DHN and NIT it was 216 nm. When a simultaneous analysis was carried out the wavelength was of 230 nm. The optimum pH were 7.90 and 7.10 when the separation of NIT and DTZ or VER and NIF were carried out, respectively, and 7.90 when a simultaneous separation was carried out. The detection limit of the assay was less than 8 ng ml⁻¹ for all compounds, with coefficients of variation less than 7% (for inter- and intra-day) over the concentration range of 1–1000 ng ml⁻¹. The retention times were less than 11 min. When NIF or NIT were studied, it was necessary to use a sodium vapour lamp in order to avoid the photodegradation which takes place under daylight conditions.     

Therapeutic monitoring of imipramine and desipramine by micellar liquid chromatography with direct injection and electrochemical detection

A micellar liquid chromatographic (MLC) procedure was developed for the clinical monitoring of imipramine and its active metabolite, desipramine. The determination of these highly hydrophobic substances was carried out after direct injection of the serum samples using a mobile phase composed of 0.15 m SDS--6% (v/v) pentanol buffered at pH 7, pumped at 1.5 mL/min into a C(18) column (250 x 4.6 mm), and electrochemical detection at 650 mV. Using this MLC method, calibration was linear (r > 0.995) and the limits of detection (ng/mL) were 0.34 and 0.24 for imipramine and desipramine, respectively. Repeatabilities and intermediate precision were tested at three different concentrations in the calibration range and a CV (%) below 2.2 was obtained. In this MLC procedure, the serum is determined without treatment, thus allowing repeated serial injections without changes in retention factors, and reducing the time and consumables required to carry out the pretreatment process. The assay method can be applied to the routine determination of serum imipramine and its metabolite in therapeutic drug monitoring.