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  • 1995-1999
  • 1990-1994  (5)
  • 1994  (5)
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 5626-5630 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report measurements of the absolute cross sections for the electron-impact ionization of the NF2 and NF free radicals from threshold to 200 eV. At 70 eV, the absolute parent NF2 and NF ionization cross section are 1.25±0.23 A(ring)2 and 1.05±0.19 A(ring)2, respectively. We found little evidence of the presence of vibrationally excited radicals in the incident target beam for both NF2 and NF. We also studied the dissociative ionization of NF2 and NF. The absolute cross section for the formation of the NF+ fragment ions from NF2 was found to be 0.75±0.15 A(ring)2 at 70 eV. The NF+ fragment ions are formed with little excess kinetic energy. The only significant pathway leading to the observed NF+ fragment ions is the single positive ion formation. Our data show no indication of the presence of double positive ion formation channels or positive–negative ion pair formation processes. Cross sections for the formation of the atomic fragment ions F+ and N+ from both NF2 as well as NF were found to be small with maximum values of less than 0.1 A(ring)2 at 70 eV in all cases.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Histochemistry and cell biology 102 (1994), S. 389-395 
    ISSN: 1432-119X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The role of oxidative stress resulting from production of reactive oxygen species and/or from suppression of the cellular antioxidant capacity in parasitic infections is shortly reviewed. The experimental part of the paper deals with the glutathione (GSH) — glutathione reductase (GR) system, a cornerstone of intracellular antioxidant defence mechanisms. For studying this system in parasitic diseases such as malaria new or modified methods are required. Total glutathione comprising GSH and glutathione disulphide (GSSG) in blood samples was assayed as follows. One volume of blood (≥10 μl) is mixed with two volumes of 5% sulphosalicylic acid; after centrifugation (5 min, 10000 g), 10 μl of supernatant is taken for spectrophotometric analysis using the 5,5′-dithiobis(2-nitrobenzoate) (DTNB)-glutathione recycling assay. When compared with the original method, the procedure reported here is more sensitive, less time-consuming, avoids unfavourable pH-values and leads to a sample which when frozen is stable for months. In a pilot study, the method was applied to 14 patients suffering from malaria caused by Plasmodium falciparum. The concentrations of erythrocyte glutathione were significantly decreased in the patients (1.42±0.47 mM, mean±SD) when compared to age- and sex-matched controls (2.11±0.45 mM, P〈0.01). The findings are contrasted with P. falciparum cultures in vitro where glutathione levels are known to be elevated. Based on the characteristics of GR a concept of determining the redox state of single cells is introduced. Microcrystals of the enzyme are expected to be suitable indicators for the intracellular redox potential since the dithiol-disulphide interconversion at the enzyme's active site is associated with a change in colour. Here we describe a simple overlay technique for crystallizing recombinant human glutathione reductase. This procedure may also be applicable to the crystallization of other proteins.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 18 (1994), S. 267-289 
    ISSN: 1573-0662
    Keywords: Atmosphere ; dimethyl sulfide ; dimethyl disulfide ; mechanism ; methane sulfonic acid ; photolysis ; smog chamber ; sulfur dioxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The products of the 254 nm photolysis of ppm levels of DMDS have been studied as a function of the O2 partial pressure at 760 Torr (N2 + O2) and 298±2 K. The major sulfur containing compounds detected were SO2 and CH3SO3H (methane sulfonic acid, MSA) and the major carbon containing compounds were CO, HCHO, CH3OH and CH3OOH (methyl hydroperoxide). Within the experimental error limits the observed sulfur and carbon balances were approximately 100%. CH3OOH has been observed for the first time in such a photooxidation system. Its observation provides evidence for the formation of CH3 radicals by the further oxidation of the CH3S radicals formed in the primary photolysis step. From the behavior of the DMDS photolysis products as a function of the O2 partial pressure, O3 concentration and added OH radical source it is postulated that the further reactions of CH3SOH (methyl sulfenic acid), formed in the reaction OH + CH3SCCH3 → CH3SOH + CH3S, are the main source of MSA in the 254 nm photolysis of DMDS. Some of the possible implications of the results of this study for the degradation mechanisms of other atmospherically important organic sulfur compounds, in particular DMS, are briefly considered.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 30 (1994), S. 115-118 
    ISSN: 1434-6079
    Keywords: 34.80.Dp
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We report measurements of the circular polarization correlation parameterP 3 for the excitation of the 4s′[1/2] j=1 state in Ar by 40 eV electrons and for the excitation of the Kr 5s[3/2] J=1 state by 30 eV electrons at electron scattering angles up to 50°. The measured Ar data are compared to predictions of a distorted wave Born approximation (DWBA). The agreement is in general not very good with theory predictingP 3 values considerably larger than the measured values in the regime of small scattering angles. In Kr, where the measured data are compared to theoretical predictions from a DWBA, a first-order many-body theory (FOMBT) and a relativistic distorted wave theory (RDW), the level of agreement between experiment and theory is somewhat better. The measuredP 3 parameters in conjunction with the previously measured linear coherence parametersP 1 undP 2 under the same scattering conditions yield the total polarizationP tot + which is a measure for the level of coherence in the excitation process. In both cases studied here, we found values of eliminateP tot + that were consistent with a fully coherent excitation process.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 26 (1994), S. 827-845 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Haloacetyl, peroxynitrates are intermediates in the atmospheric degradation of a number of haloethanes. In this work, thermal decomposition rate constants of CF3C(O)O2NO2, CClF2C(O)O2NO2, CCl2FC(O)O2NO2, and CCl3C(O)O2NO2 have been determined in a temperature controlled 420 l reaction chamber. Peroxynitrates (RO2NO2) were prepared in situ by photolysis of RH/Cl2/O2/NO2/N2 mixtures (R = CF3CO, CClF2CO, CCl2FCO, and CCl3CO). Thermal decomposition was initiated by addition of NO, and relative RO2NO2 concentrations were measured as a function of time by long-path IR absorption using an FTIR spectrometer. First-order decomposition rate constants were determined at atmospheric pressure (M = N2) as a function of temperature and, in the case of CF3C(O)O2NO2 and CCl3C(O)O2NO2, also as a function of total pressure. Extrapolation of the measured rate constants to the temperatures and pressures of the upper troposphere yields thermal lifetimes of several thousands of years for all of these peroxynitrates. Thus, the chloro(fluoro)acetyl peroxynitrates may play a role as temporary reservoirs of Cl, their lifetimes in the upper troposphere being limited by their (unknown) photolysis rates. Results on the thermal decomposition of CClF2CH2O2NO2 and CCl2FCH2O2NO2 are also reported, showing that the atmospheric lifetimes of these peroxynitrates are very short in the lower troposphere and increase to a maximum of several days close to the tropopause. The ratio of the rate constants for the reactions of CF3C(O)O2 radicals with NO2 and NO was determined to be 0.64 ± 0.13 (2σ) at 315 K and a total pressure of 1000 mbar (M = N2). © 1994 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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