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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 78 (1966), S. 452-452 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 5 (1966), S. 425-426 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 381 (1971), S. 40-56 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Several unknown salts of s-triazine were prepared by different methods and the IR spectra of most of these salts were assigned. When s-triazine was reacted with HCl or HBr, mixtures were obtained which consisted of s-triazinium-monohalogenides and products with higher contents of hydrohalogenides. When s-triazine was reacted with HJ, a product C3H3N3 · 3 HJ was obtained. The IR spectra of this compound and of the corresponding compound with DJ were taken to interprete the structure. Addition compounds of s-triazine with several ansolvo-acids were produced in which one or two ansolvo-acid molecules were bound to one molecule of s-triazine. The IR spectra of some of said addition compounds were assigned. Moreover, an adduct of bromine and s-triazine, C3H3N3 · Br2, was prepared.
    Notes: Nach verschiedenen Methoden wurden einige unbekannte Salze des s-Triazins dargestellt und die IR-Spektren der meisten Salze zugeordnet. Bei der Umsetzung von s-Triazin mit HCl oder HBr bildeten sieh Gemische aus s-Triazinium-monohalogeniden und Produkten mit höherem Halogenwasserstoffgehalt, mit HJ wurde dagegen die Verbindung C3H3N3 · 3 HJ erhalten. Die IR-Spektren dieser Verbindung und des entsprechenden Produkts aus s-Triazin und DJ ergaben Anhaltspunkte für die Struktur. Die Umsetzung einiger Ansolvosäuren mit s-Triazin führte zu Additionsverbindungen, in denen ein aber auch zwei Ansolvosäuremoleküle an ein Molekül s-Triazin gebunden waren. Die IR-Spektren der meisten Additionsverbindungen wurden ebenfalls zugeordnet. Außer dem wurde ein Addukt von Brom an s-Triazin. C3H3N3 · Br2, dargestellt.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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