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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 123 (1992), S. 325-331 
    ISSN: 1434-4475
    Keywords: Azide ; Crystal structure ; Dimethylpyridine ; Zinc
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Three adducts of zinc azide with 2,4-/3,4- and 3,5-dimethylpyridine (DMP), respectively, were prepared and the crystal structures determined by single crystal X-ray diffraction methods. The three compounds crystallize in the monoclinic space group P21/c withZ=4: Zn(N3)2·2,4-DMP at 300 (2) K:a=1 098.6(4),b=1 600.2(6),c=608.8(3) pm, β=102.47(3)°;R=0.071 (R w =0.056). Zn(N3)2·3,4-DMP at 103 (3) K:a=1 102.1(3),b=1 649.0(4),c=611.8(1) pm, β=104.54(2)°;R=0.055 (R w =0.051). Zn(N3)2·3,5-DMP at 97 (3) K:a=602.1(2),b=2 037.9(7),c=853.8(3) pm, β=90.77(3)°;R=0.069 (R w =0.055). The molecular geometry is similar for the three adducts, but the packing of theDMP-molecules is different. The zinc atoms are surrounded by five nitrogen atoms, four belonging to the azide groups and one to theDMP-adduct. The trigonal bipyramidal shaped ZnN5-polyhedra share common edges to form chains.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 723-728 
    ISSN: 0009-2940
    Keywords: 1,8-Diaminonaphthalenes, X-ray structure analysis of, conformational barriers of, dynamic behavior of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compounds 2 and 3 have been synthesized from 1,8-diaminonaphthalene. The molecular structure of 2 has been determined by X-ray structure analysis and is discussed with regard to the arrangement of the peri-diphenylamino substituents in the crystalline state and the steric strain in the molecule. NMR studies of 3 reveal two conformational processes. Their nature is discussed and barriers are reported.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 30 (1992), S. 84-86 
    ISSN: 0749-1581
    Keywords: ESR ; Nitrogen-centred radicals ; 2,3-Dihydro-1-oxo-1λ4,2,3,5-thiatriazol-3-yl radicals ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dehydrogenation of 2,5-dihydro-1,2,3,5-thiatriazole 1-oxides with thermally formed bis(4-methylphenyl)aminyl generated 2,3-dihydro-1-oxo-1λ4,2,3,5-thiatriazol-3-yl radicals. ESR, ENDOR and triple resonance studies in combination with 15N labelling yielded the magnitude and assignment of all 1H and 14N hyperfine coupling (HFC) constants. The radicals have a basic five-π-electron amidrazon-2-yl structure with the highest spin density at N-2.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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