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  • 2015-2019
  • 1975-1979  (3)
  • 1965-1969
  • 1930-1934
  • 1900-1904
  • 1860-1869
  • Saturated organic compounds, MO treatment of ∼  (3)
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Erscheinungszeitraum
  • 2015-2019
  • 1975-1979  (3)
  • 1965-1969
  • 1930-1934
  • 1900-1904
  • +
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 43 (1977), S. 287-297 
    ISSN: 1432-2234
    Schlagwort(e): Hybrids, linear combination of ∼ ; Saturated organic compounds, MO treatment of ∼ ; Spectra, far ultraviolet
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract A LCHO SCF-CI semiempirical scheme is formulated for compounds of carbon and hydrogen, and far-UV transition energies computed for a number of acyclic alkanes. The type of spectral bands (CH → CH*, etc.) and symmetries of subbands are assigned, and their dependence on conformation and branching discussed. It is argued that, for pentanes and higher alkanes, spectral quantities can be estimated from data on the lower alkanes.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 45 (1977), S. 45-52 
    ISSN: 1432-2234
    Schlagwort(e): Hybrids, linear combination of ∼ ; Saturated organic compounds, MO treatment of ∼ ; Spectra, far ultraviolet ∼ ; Cyclobutane, auxochromic effect of ∼
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Spectral quantities of cyclopropane, cyclobutane, cyclohexane, and of several derivatives, have been calculated by a semiempirical all-valence electron SCF-CI MO method. In cyclopropane, HOMO is practically localized in the carbon-frame, and LVMO is purely so. In cyclobutane, these two MO's are based on C-H bonds, while cyclohexane holds an intermediate position. Despite the overall similarity-experimental and computed-of the spectra of these molecules, assignments are non-parallel. Like cyclopropane, cyclobutane can extend conjugation, but to a diminished degree; cyclohexane behaves in this respect like an acyclic alkane. An interpretation of this gradation, in terms of the nature of high-lying MO's, is proposed.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 47 (1978), S. 27-38 
    ISSN: 1432-2234
    Schlagwort(e): Hybrids, linear combination of ∼ ; Saturated organic compounds, MO treatment of ∼ ; Small rings ; Carbonyl stretching frequency
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract In the frame of our studies on small-ring compounds, we deal here with structures in which a three-membered ring and a carbonylated four-membered ring are fixed in close proximity. The theoretical approach is through an allvalence electron semiempirical method. The experimental background, based on results of other workers, comprises mainly UV and IR spectral data. The main topics to be discussed are: charge-donation and charge-transfer from the 3-ring, hypsochromic and bathochromic shifts of electronic transitions related to the carbonyl, direct substituent effects on the carbonyl stretching frequency, and the across-ring interaction in cyclobutanone.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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