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  • Artikel  (2)
  • Photochemistry  (1)
  • azacage  (1)
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  • Artikel  (2)
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 12 (1992), S. 263-274 
    ISSN: 1573-1111
    Schlagwort(e): Alkalide ; electride ; azacage ; cryptand ; sodium NMR ; lithium NMR
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The new lithium-selective complexant 5,12,17-trimethyl-1,5,9,12,17-pentaazabicyclo[7.5.5]nonadecane (TMPAND) was used to synthesize Li+(TMPAND)Na−, the first alkalide prepared from an azacage complexant. This sodide was characterized by a variety of methods. Differential scanning calorimetry experiments showed a reversible, endothermic, solid-solid phase transition at an onset temperature of −75 ± 3°C and with ΔH = 3.3 ± 1 kJ/mol.23Na NMR spectra showed a peak at −61 ppm, characteristic of a sodium anion, and a second minor peak at −10 ppm, probably due to the interaction of Na- with trapped electrons. The quadrupole coupling constant of the complexed lithium cation was found to be 0.19 MHz at −100°C, and7Li NMR spectra showed a discontinuity in the line width of the7Li NMR peak and in the quadrupole coupling constant at the phase transition.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1911-1918 
    ISSN: 1434-1948
    Schlagwort(e): Macrocycles ; Photochemistry ; Fluorescence spectroscopy ; Coordination chemistry ; Zinc ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The macrocyclic ligands L2 and L3, containing a triethylenetetraamine and a tetraethylenepentaamine moiety linked to the methyl groups of 2,9-dimethyl-1,10-phenanthroline, bind H+ and Zn2+ ions giving rise to modulation of the fluorescence emission intensity. The equilibrium constants and the enthalpy changes for ligand protonation were determined by means of pH-metric and microcalorimetric methods in 0.1 M Me4NCl solutions at 298.1±0.1 K. Also the stability constants of the Zn2+ complexes were determined under the same experimental conditions. L2 forms only mononuclear complexes, while L3 also forms dizinc(II) species. The phenanthroline group has fluorescence emission properties, but interaction with the lone pairs of benzylic nitrogen atoms produces an efficient quenching of the emission. Such a quenching effect can be avoided by deactivation of the benzylic nitrogen atoms by means of protonation or Zn2+ complexation. Hence, L2 and L3 behave as chemosensor for H+ and Zn2+, the photochemical properties of the ligands being modulated by the formation of different protonated and complexed species. In the case of L3, the fluorescence emission is also controlled by the metal to ligand molar ratio, because of the formation of an emissive binuclear complex.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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