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  • 1995-1999  (2)
  • 1
    Electronic Resource
    Electronic Resource
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The analysis of various spirits using a GC-IR-MS coupling permits the qualitative description of their constituents based on their characteristic spectra. Sample preparation, instrumentation, experimental parameters and peak identification using a combined library search are described.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1995 (1995), S. 1515-1519 
    ISSN: 0947-3440
    Keywords: Macrocycles ; Recognition ; Piperazines ; Self-assembly ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New large, up to 45-membered macrocycles were synthesised from piperazine and m- and p-2,6-bis(bromomethyl)xylene under high dilution conditions. X-ray structures of compounds 3a, 4a, 5a, and 8b were determined. Surprisingly, none of the macrocycles prepared showed any inclusion properties towards small guest molecules. Instead, the compounds were found to self-organize during the packing process into larger structures due to the complementary of the molecular skeletons. In the crystalline state 3a forms nets, where the macrocycles are bound by H—C—H…N interactions to each other. 4a exits in a dimeric structure, which, in turn, further extends to a sheet structure. The positively charged phane 8b (di-dihydrochloride salt) adopts a chair-chair conformation, confirming that protonation of the N atoms does not change the conformation.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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