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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Monatshefte für Chemie 111 (1980), S. 63-79 
    ISSN: 1434-4475
    Schlagwort(e): Chromium(III)complexes ; Iron(II)complexes ; Magnetic susceptibility measurements ; Mössbauer spectra
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Zusammenfassung Es wurden Komplexe von Pyridin-2-aldoxim (Hpox) mit Fe(II) und Cr(III) vom Typ [Fe(Hpox)2 X 2] (X=Cl, Br, I, NCS), [Cr(Hpox)3]Cl3·3 H2O, [Cr(Hpox)2 X 2]ClO4 (X=F, Cl, Br) und [Cr(Hpox)2(H2O)2]Br3·H2O hergestellt. Charakterisierung und Diskussion von Geometrie und Bindungsverhalten in den Komplexen erfolgte auf Grund von analytischen Daten, Röntgen-Pulveraufnahmen, Elektronenanregungsspektroskopie, Infrarotspektroskopie, magnetischen Messungen undMössbauer-Spektroskopie.
    Notizen: Abstract Complexes of pyridine-2-aldoxime (Hpox) with iron(II) and chromium(III) of type, [Fe(Hpox)2 X 2] (X=Cl, Br, I or NCS); [Cr(Hpox)3]Cl3·3 H2O; [Cr(Hpox)2 X 2]ClO4 (X=F, Cl or Br) and [Cr(Hpox)2(H2O)2]Br3·H2O were prepared and characterized by analytical X-ray powder diffraction, magnetism, vibrational (conventional and far-infrared) and electronic spectroscopy techniques. X-ray and electronic spectral data indicate that all the complexes except [Cr(Hpox)3]Cl3·3 H2O havetrans-pseudo-octahedral microsymmetry around the metal ion. Infrared spectral data indicate that the ligand, Hpox, behaves like a neutral ligand and coordinates to the metal ion through pyridine nitrogen atom and oxime nitrogen atom in all these complexes. The magnetic susceptibilities of chromium(III) complexes, measured over a temperature range 300–78 K, are independent of temperature whereas the magnetic moments of iron(II) complexes over a temperature range 300–20 K are dependent of temperature. The observed temperature dependence of magnetic moments of iron(II) complexes was used to evaluate the magnitude of orbital reduction factor,k, the low-symmetry distortion parameter, Δ, and the extent of reduction in spin-orbital coupling, λ. In all these iron(II) complexes the magnetic results indicate the presence of an orbitally non-degenerate,5B2g, ground state. Magnetically unperturbed and perturbedMössbauer spectra of iron(II) complexes at various temperatures have also been reported. Magnetically perturbedMössbauer spectra of iron(II) complexes at 4.2 K in an axial field of 60kGauss indicate that the principal component of electric field gradient tensor is positive and consistent with5B2g ground electronic state in a tetragonal (D 4h) local site symmetry.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Genetic resources and crop evolution 46 (1999), S. 73-79 
    ISSN: 1573-5109
    Schlagwort(e): Erianthus ; genetic diversity ; phylogeny ; RAPD-PCR ; Saccharum complex
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft
    Notizen: Abstract Molecular diversity in Saccharum complex was studied using 195 RAPD markers generated by 12 random primers. Among the Saccharum species, S. officinarum showed a low level of genetic diversity while S. sinense was found to be more diverse. Six taxonomical groups were clearly resolved in the cluster analysis. S. officinarum, S. robustum, S. spontaneum and Erianthus spp. formed discrete groups. S. barberi and S. sinense formed a single cluster, so also Narenga and Sclerostachya. S. officinarum was found to be closer to S. robustum and distant from S. spontaneum. Among the related genera, Sclerostachya was closer to Saccharum while Erianthus was found to be highly divergent from all the Saccharum species. Six of the primers used generated RAPD fragments unique to Erianthus. It is suggested that the Erianthus spp. can contribute substantially towards sugarcane varietal improvement in view of its greater divergence with Saccharum.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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