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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 136 (1989), S. 159-168 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Mössbauer spectra of /pheophytinato a/ iron/III/ chloride [Fe/Pheo-a/Cl] and /pheophytinato b/ iron/III/ chloride [Fe/Pheo-b/Cl] have revealed that the central iron/III/ ion is in a high-spin state and axially coordinated by chloride ions in solid phase. Temperature-dependent asymmetry observed for the quadrupole splitting doublet of iron/III/ pheophytins, i.e., Fe/Pheo-a/Cl and Fe/Pheo-b/Cl, is interpreted on the basis of the zero-field splitting. The structural difference between iron/III/ pheophytins and iron/III/ porphyrins is reflected in the quadrupole splitting more than in the isomer shift. Magnetic behaviour of iron/III/ pheophytins near 4.2 K is very similar to that of iron/III/ porphyrins.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 137 (1989), S. 277-286 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract /Pyropheophytinato a/ iron/III/ chloride [Fe/Pyropheo-a/Cl] and /pyropheophytinato b/ iron/III/ chloride [Fe/Pyropheo-b/Cl] have been prepared and characterized by Mössbauer spectroscopy. The Mössbauer parameters of the iron/III/pyropheophytins are similar to those of iron/III/ porphyrins. A comparison of the quadrupole splittings for the iron/III/ pyropheophytins with those for the iron/III/ pheophytins suggests that the deviations of the cyclopentenone ring and the saturated pyrrole ring from the macrocyclic plane become smaller with the removal of the methoxycarbonyl group.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of legal medicine 102 (1989), S. 437-444 
    ISSN: 1437-1596
    Keywords: Fetal hemoglobin, identification in blood stains ; Blood stains, identification of fetal hemoglobin ; Fetales Hämoglobin, in Blutspuren ; Blutspuren, Nachweis von fetalem Hämoglobin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Law
    Description / Table of Contents: Zusammenfassung Es wurde eine neue Methode zur Identifizierung von fetalem Hämoglobin (Hb F) in Blutspuren mit der umgekehrten Phase-Hochleistungsflüssigkeitschromatographie durchgeführt. Die Unterscheidung zwischen fetalen Blutspuren und denen von Erwachsenen erfolgte aufgrund der Existenz der Spitzen der γ-Ketten von Hb F. In den Chromatogrammen der untersuchten Blutspuren von Erwachsenen traten fast keine γ-Ketten auf. Diese Methode ermöglichte ferner die Bestimmung des Hb F-Wertes mit dem Flächenverhältnis der Globin-Ketten auf den Chromatogrammen. Hb F-Werte der sechs Fälle von Nabelschnurblutspuren auf dem Filterpapier lagen zwischen 81.1% und 91.3%. Die vorliegende Untersuchung zeigt, daß sich der Hb F-Wert für mindestens 12 Wochen nicht ändert. In der Praxis der Rechtsmedizin ist diese Methode im Hinblick auf die Einfachheit, hohe Empfindlichkeit, Schnelligkeit und Zuverlässigkeit sehr wertvoll.
    Notes: Summary A new method for the identification of fetal hemoglobin (Hb F) in blood stains by reverse-phase high performance liquid chromatography is described. Differentiation between fetal and adult blood stains is based on the existence of γ-chain peaks which are characteristic of Hb F. Very few γ chains appeared on chromatograms of all the adult blood stains examined. The level of Hb F could be determined by measuring the total of chromatogram γ-globin chain areas, and expressing it as a percentage of total Hb. Levels in six cord blood stains on filter paper ranged from 81.1% to 91.3% and remained constant for at least 12 weeks. This method is of great value for its simplicity, sensitivity and speed, and most importantly for its reliability in the field of forensic medicine.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Hyperfine interactions 46 (1989), S. 723-731 
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The mixed-valence state of Prussian blue and its thermal decomposition products has been studied by Mössbauer and infrared spectra, and X-ray powder diffraction and conductivity measurements. The57Fe Mössbauer spectra have revealed that the coordination environment of Prussian blue is not changed by the heat-treatment at lower than 200°C while the flipping of the cyano ligands takes place when the heat-treatment temperature exceeds 250°C. The electrical conductivity of the Prussian blue samples heat-treated in vacuo at 300 and 350°C is higher than that of the samples heat-treated at lower temperatures. All the spectral measurements have demonstrated that a new mixed-valence state is produced in Prussian blue by thermally flipping the cyano ligand and quenching the flipped cyano ligand to liquid nitrogen temperature.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chlorophyll-bonded stationary phase ; Cyano(pheophytinato a)cobalt(III) ; Pheophytin a
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The separation and determination of the nitrite ion by affinity chromatography is described. The good separation of the nitrite ion was obtained by using cyano-(pheophytinato a)cobalt(III) bonded octadecylsilica as the stationary phase and water of pH 4.3 adjusted by acetic acid as the mobile phase. Conventional ion chromatograph was also used for the analysis of the nitrite ion. For the synthetic samples prepared by mixing the nitrite and nitrate ions, analytical values obtained by affinity chromatography were in agreement with calculated values and close to the analytical values obtained by ion chromatography. In the proposed affinity chromatography, the nitrite and nitrate ions could be determined in the concentration range of 0.15–1.0ppm and 0.1–1.0ppm with relative standard deviations (n=10) of 5.3% and 4.7%, respectively.
    Type of Medium: Electronic Resource
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