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  • Analytical Chemistry and Spectroscopy  (2)
  • Conformation  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 21 (1983), S. 42-45 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of a number of pyridazine derivatives have been recorded in DMSO-d6 solution and analysed. Examination of the most diagnostic resonances, with particular emphasis on those arising from the pyridazine ring system, enabled the ready establishment of the presence of a ring-chain tautomerism in 5-(o-aminophenylcarbamoyl)pyridazine-4-carboxylic acid, methyl 5-(o-aminophenylcarbamoyl)pyridazine-4-carboxylate, 5-(o-aminophenylcarbamoyl)-3,6,-dimethylpyridazine-4-carboxylic acid and 5-(2-amino-1,2-dicyanovinylenecarbamoyl)pyridazine-4-carboxylic acid. This gave rise to 3′,4′-dihydro-3′-oxospiro[pyridazine-5(2H),2′(1H)-quinoxaline]-4-carboxylic acid, methyl 3′,4′-dihydro-3′oxospiro[pyridazine-5(2H),2′(1′H)-quinoxaline]-4-carboxylate, 3′,4′-dihydro-3′-oxo-3,6-dimethylspiro[pyridazine-5(2H), 2′(1′H)-quinoxaline]-4-carboxylic acid and 5-oxo-2,3-dicyano-1,4,8,9-tetraazaspiro[5.5]undeca-2,7,10-triene-11-carboxylic acid, respectively.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0749-1581
    Keywords: Selective relaxation time ; Double-selective relaxation time ; Conformation ; Dynamics ; Cinnamide derivative ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dynamics and conformation ofN,N-dimethyl-N-[3-(4-methoxy-trans-cinnamoylamino)propyl]-N-n-dodecylammonium bromide (1) have been established in two solvents (CDCl3 and DMSO-d6) by the use of 13C spin-lattice relaxation rates, non-selective and selective proton spin-lattice relaxation rates and 1H-(1H) NOE experiments. The two solvents affect the conformation of the cinnamide moiety in different ways. This alters the anchor capacity of the moiety towards the alkyl chain and, as a consequence, the dynamics of 1 in CDCl3 and DMSO-d6 show understandable differences. However, the main mean conformations of 1 in both solvents are ‘linear’. The data do not allow the rationalization of the relationship between conformation and sunscreen efficiency.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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