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  • Inorganic Chemistry  (2)
  • Carotenoids
  • 1975-1979  (2)
Collection
Keywords
  • Inorganic Chemistry  (2)
  • Carotenoids
  • Chemistry  (2)
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 3215-3221 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 13C NMR Spectroscopy of Norbornane Derivatives, II: The Influence of Homoconjugative Interactions on the Carbonyl Chemical Shifts in NorbornanonesThe 13C-NMR chemical shifts of several norbornanone derivatives with exo- or endo-cyclopropane rings, endo-cyclobutane rings, and/or double bonds are reported. The effects of cross conjugation of the carbonyl group with a double bond results in a significant upfield shift of the signals of C-7 (large) and of the olefinic carbon atoms (small). In this regard the carbonyl compounds are closely related to nonclassical 7-norbornyl cations. The 13CO shifts are discussed in relation to other molecular properties: rates of solvolysis of 7-substituted norbornane derivatives, decarbonylation rates, n,π* excitation energies, and photoelectron spectra.
    Notes: Es wird über die 13C-NMR-chemischen Verschiebungen von Norbornanonderivaten mit exo- oder endo-Cyclopropanringen, endo-Cyclobutanringen und/oder Doppelbindungen berichtet. Die gekreuzte Konjugation von Carbonylgruppe und Doppelbindung verursacht eine relativ starke Hochfeldverschiebung der Signale von C-7 und eine geringere der olefinischen C-Atome. Aus dieser Sicht verhalten sich die Carbonylverbindungen ähnlich wie die nichtklassischen 7-Norbornyl-Kationen. Die 13CO-Verschiebung wird mit anderen molekularen Eigenschaften in Beziehung gesetzt: Solvolysegeschwindigkeit von 7-Norbornylderivaten, Decarbonylierungsgeschwindigkeiten, n,π*-Anregungsenergien und Photoelektronenspektren.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 2708-2721 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Influence of Substituents on sigmatropic Reactions, I. 3-Methylhomotropilidene. Synthesis and EquilibriumAccording to 1H- and 13C n.m.r. spectroscopy 3-methylhomotropilidene (1b) is favored relative to 1-methylhomotropilidene (2b) in the thermal equilibrium. The quantitative interpretation of the 13C-n.m.r. spectra yields ΔH° = 1.6 ± 0.3 kcal/mole, ΔS° = 2.0 ± 0.7 Clausius and ΔG2730 = 1.05 ± 0.05 kcal/mole. EHT-calculations are utilized to understand these results. - The synthesis of the title compound and the unsubstituted homotropilidene 1a is achieved via hydrolysis of the acetals 3 yielding the thermally unstable ketones 4, the treatment of which with diazomethane/CuCl yields 5, which are decarbonylized on heating to the homotropilidenes 1.
    Notes: Im thermischen Gleichgewicht ist das 3-Methylhomotropiliden (1b) gegenüber dem 1-Methyl-homotropiliden (2b) nach Auskunft der 1H-und 13C-NMR-Spektren bevorzugt. Die quantitative Auswertung der 13C-NMR-Spektren liefert ΔH° = 1.6 ± 0.3 kcal/mol, ΔS° = 2.0 ± 0.7 Clausius und ΔG2730 = 1.05 ± 0.05 kcal/mol. EHT-Berechnungen werden zur Deutung dieses Befundes herangezogen. - Die Herstellung der Titelverbindung und des unsubstituierten Grundkörpers 1a erfolgt durch Hydrolyse der Acetale 3 zu den thermolabilen Ketonen 4, die mit Diazomethan/CuCl zu 5 homologisiert werden. Die Thermolyse ergibt die Homotropilidene 1.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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