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  • Analytical Chemistry and Spectroscopy  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 1 (1969), S. 319-327 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The NMR spectra of fifteen para-substituted acetanilides, XC6H4·NH·CO·CH3 (X = NH·CO·Me; NH2; CO·OEt; COOH; Cl; OEt; F; H; OMe; CH3; NO2; C6H5; —N=N—C6H5; Me3Si), have been recorded. δCH3 and δNH are linearly related to Hammett's σp constant. The coupling J (o-H—H) between aromatic protons is mainly dependent on σR0. J(13C—H), in methyl group is approximatively constant in the series.
    Notes: Les spectres de RMN de quinze acétanilides para-substitués XC6H4·NH·CO·CH3 (X = NH·CO·ME; NH2; CO·OEt; COOH; Cl; OEt; F; H; OMe; CH3; NO2; C6H5;—N=N—C6H5; Me3Si) ont été étudiés. Il y a une relation linéaire entre δCH3 et δNH et les constantes σP de Hammett. Le couplage J(o-H—H) entre les protons aromatiques est relié plutôt à σR0. La constante J (13C—H) dans le groupe CH3, est indépendante de X.
    Additional Material: 5 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. 259-263 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: High field NMR spectroscopy, double resonance and INDOR experiments are used for unambiguous assignment of the endo configuration of 3-trimethylsilyl-5-norbornene. Chemical shifts and coupling constants have been accurately determined and tested by computer simulation. Some ‘non W’ long range couplings are demonstrated.
    Notes: La RMN à 250 et à 300 MHz combinée à des expériences de double irradiation de type classique ou INDOR a été utilisée pour établir sans ambiguité la structure endo d'un triméthylsilyl-3 norbornène-5. Les déplacements chimiques et les constantes de couplage ont été très exactement déterminés, des couplages à longue distance n'obéissant pas à la ‘règle du W’ ont été mis en évidence.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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