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  • Carbocation  (1)
  • alkane activation  (1)
  • Springer  (2)
  • American Institute of Physics
  • Nature Publishing Group
  • 1995-1999  (2)
  • 1965-1969
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Verlag/Herausgeber
  • Springer  (2)
  • American Institute of Physics
  • Nature Publishing Group
Erscheinungszeitraum
  • 1995-1999  (2)
  • 1965-1969
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Molecular engineering 7 (1997), S. 429-438 
    ISSN: 1572-8951
    Schlagwort(e): Carbocation ; zeolite ; acidity ; electrostatic field
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Theoretical studies, at MNDO level, of carbocations adsorbed over a zeolite active site were carried out, taking into account the effect of electrostatic fields. Clusters 1 and 2 were placed between two electrostatic charges of opposite sign. The distance from each charge to the center of the oxygen atom bearing the proton or alkyl group was varied in order to find the minimum in energy. The ionicity, expressed by the decrease in bond order, slightly increased with the inclusion of the charges. A more pronounced effect was observed for a positive charge of +2. The energy of the system decreased with the introduction of electrostatic charges. This fact may be partly explained by the electrostatic interaction between the opposed charges and also to an observed increase in the Si–-O–-Al bond angle, decreasing the steric repulsions between the substituents and the acid site. The bond orders remained high, indicating a predominant covalent character for the adsorption of the carbocations. The calculations are in agreement with experimental data of exchange of polyvalent cations, which pointed to an increase in the acid strength of the zeolite, due to decrease in the electron density in the aluminum atom.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 1572-9028
    Schlagwort(e): carbonium ion ; superacid ; rearrangement ; alkane activation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract A theoretical ab initio study of the interconversion of pentacoordinated carbonium ions was carried out. For the isobutonium cations it was found that the respective C-carbonium ions were lower in energy than the H-isobutonium ions. Nevertheless, the interconversion of the 1-H-isobutonium cation in the C-isobutonium ion is a barrierless process. This suggests that product arisen from C–C protonation in liquid superacid and zeolite catalyzed alkane activation may be formed by protonation in the outer and more accessible primary C–H bonds of isobutane, rather than by direct protonation of the inner and more steric demanding C–C bonds.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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