Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Organic Chemistry  (1)
  • electron acceptors  (1)
  • 1
    ISSN: 1572-879X
    Schlagwort(e): spinel structure ; ferrites ; pyridine methylation ; electron acceptors
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract A series of Ni–Co ferrites with the general formula Ni1-x Co x Fe2O4 (x = 0, 0.2, 0.5, 0.8 and 1.0) was prepared by a low-temperature hydroxide coprecipitation route. The catalyst systems were characterized by adopting various physico-chemical techniques. Alkylation of pyridine with methanol was carried out in a down-flow vapor-phase reactor. The influence of surface acid–base properties, cation distribution in the spinel lattice and various reaction parameters are discussed. It was observed that the systems possessing x values ≥0.5 are selective for 3-picoline formation, whereas the ones with x values 0 and 0.2 give a mixture of 2- and 3-picolines. Pyridine conversion increased with the progressive substitution of Ni2+ ions by Co2+ ions. Cation distribution in the spinel lattice influences their acidic and basic properties, and these factors have been adequately considered as helpful to evaluate the activity of the systems.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 377-384 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: N-Substituted carbonimidodithioic acid dimethyl esters, when reacted with an active methylene compound such as nitromethane, undergo carbon-carbon bond formation followed by carbon-sulphur bond cleavage in the presence of zeolite catalysts to give 1-substituted amino-1-methylthio-2-nitroethenes. This carbon-sulphur bond cleavage is facilitated by the presence of rare earth cations in the zeolite-Y framework. The shape selectivity of the zeolite also plays an important role in this cleavage reaction. Force field calculations adopted for the molecules involved in the reaction indicate the geometry and conformational flexibility of these molecules. The computer-simulated model for the zeolite-Y is correlated with the conformation and shape of the reactant and product molecules to explain the variation in yields obtained in the conversion of substituted dimethyl esters.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...