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  • Articles  (2)
  • Articles: DFG German National Licenses  (2)
  • 1,3,2-Dithiazol-2-yl radicals  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 385-387 
    ISSN: 0009-2940
    Keywords: 1,3,2-Dithiazol-2-yl radicals ; Sulfur-nitrogen compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-Substituted 1,3,2-Dithiazoles - Precursors for 1,3,2-Dithiazol-2-yl Radicals2-Arylsulfonyl-1,3,2-dithiazoles (4) are suitable starting materials for the synthesis of 1,3,2-dithiazole-2-yl-radicals by thermal or chemical cleavage reactions. Starting with silver dithiolato complexes or with 1,2-dithioles, compounds of type 2 are formed by reaction with N,N-dichlorarylsulfonamides. This procedure allows the synthesis of even such representatives of 4 for which the corresponding disulfenyl chlorides are not accessible.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0749-1581
    Keywords: ESR ; 1,3,2-Dithiazol-2-yl radicals ; Pyrazine ; Quinoxaline ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several symmetrical 1,3,2-dithiazol-2-yl radicals have been examined that have in common nitrogen-containing substituents at the 4- and 5-positions, namely 4,5-dicyano-1,3,2-dithiazol-2-yl, [15N2]-1,3,2-dithiazolo [4,5-b] pyrazin-2-yl and 1,3,2-dithiazoleo [4,5-b] quinoxalin-2-yl. The ESR spectrum of the 4,5-dicyano radical does not reveal any 14N splittings from the cyanide groups; however, the pyrazine and the quinoxaline derivatives do have multi-lined well resolved spectra arising from substantial hyperfine interactions with these nuclei. The interactions are sufficiently large to be observed in the powder spectra of the latter. The presence of proton hyperfine interactions shows that unpaired-electron spin density is delocalized over all the rings. It has been found that the radicals attached to pyrazine and quinoxaline can be incorporated into single crystals of naphthalene and phenazine, respectively.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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