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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 6 (1974), S. 245-249 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton NMR spectra of the carbanions of xanthene [XH]- and thioxanthene [TxH]- have been recorded and interpreted. Paratropism in the central rings of [XH]- and [TxH]- is inferred from a comparison of the chemical shifts with those of the carbanion of 9,10-dihydroanthracene [AH]-. The contributions to the chemical shifts arising from n-electron excess charges, local dipoles and magnetic anisotropies are discussed. Numerical values for the various ring currents have been estimated by a least squares analysis of the observed chemical shifts after applying corrections for the excess charge effect. The results point to a strongly increasing paramagnetic ring current in the central ring in the order [AH]-, [TxH]-, [XH]-.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 6 (1974), S. 574-576 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton exchange reaction between the indenyl carbanion and its parent compound indene has been studied by NMR as a function of temperature. The rate of this bimolecular reaction is very low and has been found to be strongly dependent on the polarity of the solvent. In solvents like dimethoxyethane (∊ = 7·2) and diglyme the reaction becomes manifest in the NMR spectrum only at elevated temperatures (T 〉 150°C). In hexamethylphosphortriamide (∊ = 30) the rate is much greater and line broadening may be observable at room temperature. The reaction in this solvent is characterised by a frequency factor f = 7 × 107 1 mol-1 s-1, an activation enthalpy ΔH ≠ = 9·5 kcal mol-1 and an entropy of activation ΔS≠ = -23 e.u. The low reaction rate and its solvent dependence are briefly discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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