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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1976), S. 1047-1055 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The fragmentation mechanisms of oxazole have been studied in detail on using various experimental techniques (refocusing of metastable ions, deuteration, AP measurements) and by theoretical calculations.
    Notes: Les mécanismes de fragmentation de l'oxazole ont été précisés par diverses techniques expérimentales (refocalisation des ions métastables, deutériation, mesures de PA) et par le calcul.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-193X
    Keywords: Cyclo-bis-intercaland ; Acridine units ; cis/trans-Azobenzene dicarboxylic acids ; Inclusion compounds ; X-ray structure ; Molecular recognition ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The water soluble acyclic 1 and macrocyclic 2 receptor molecules, based on acridine units, form 1:1 complexes with the cis- or trans-2,2′ and 3,3′-azobenzene dicarboxylate substrates. The stability constants of these complexes, determined by 1H NMR spectroscopy, cover a wide range from 30 to 105M-1, thus displaying very pronounced structure selectivity with respect to both substitution pattern and cis, transconfiguration. The complexes of the cyclo-bis-intercaland receptor 2 are two or three orders of magnitude more stable than those of 1. The inclusion complex of cyclo-bis-intercaland 2 with trans-3,3′- azobenzene dicarboxylate has been isolated and its structure has been determined by X-ray crystallography using synchrotron radiation, confirming the intercalation of the substrate between the acridine residues in the species formed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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