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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1373-1377 
    ISSN: 0009-2940
    Keywords: Thionitrosyl azide ; Thiazyl azide ; Nitrosyl azide ; Tetranitrogen sulfide ; Calculations, ab initio ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stimulated by the recent detection of nitrosyl azide (N3—N=O), we investigated the stability of the sulfur analogues thionitriosyl azide (N3—N=S) and thiazyl azide (N3—S≡N) by using ab initio MO calculations up to the QCISD(T)/6-311+G(d)//QCISD/6-311G(d) + ZPE level. Both azides have a similar energy content. While thionitrosyl azide is not stable with respect to N2 elimination, thiazyl azide resists to this process by an energy barrier of about 110 kJ/mol. The NS and N3 fragments resulting from homolytic cleavage lie about 100 kJ/mol above the azides. The five-membered ring is thermodynamically much more stable than both azides but kinetically unstable with respect to cheletropic decomposition yielding N2S + N2. Overall, trans-thiazyl azide is the most likely candidate for experimental observation of, for example, the reaction of NS+ salts with the azide anion. IR wavenumbers of the azides were also predicted.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 11 (1998), S. 350-355 
    ISSN: 0894-3230
    Keywords: 1,3-dipoles ; cumulenes ; infrared spectroscopy ; mass spectrometry ; flash vacuum thermolysis ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the direct investigation of reactive intermediates it is particularly valuable to use a combination of several spectroscopic techniques. This commentary highlights recent examples, using primarily flash vacuum thermolysis for the generation of the intermediates, and matrix IR spectroscopy in conjunction with gas-phase mass spectrometric methods for their identification. The examples include nitrile imines, nitrile ylides, nitrile sulfides and selenides, dinitrogen sulfide and several novel cumulenes (X=C=C=Y, RN=C=C=C=X). © 1998 John Wiley & Sons, Ltd.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 2 (1996), S. 1318-1329 
    ISSN: 0947-6539
    Keywords: cumulenes ; heterocumulenes ; ketenimines ; matrix isolation ; thermolysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Flash vacuum thermolysis (FVT) of suitably substituted isoxazol-5(4H)-ones 7-9 leads to three different types of ketenimines, namely, the isoxazolonoketenimines 2, the novel bisiminopropadienes RN=C=C=C=NR (5), and the C-cyanoketenimines 14, all characterized by a combination of FVT/matrix isolation/IR spectroscopy and FVT/MS. An unusual, linear C=C=N-C backbone in ketenimines 2g and 2h is revealed by their exceptional spectroscopic properties as well as an X-ray crystal structure of 2g, and confirmed by density functional calculations (B3LYP/6-31 G*); these compounds are best described as resonance hybrids of ketenimines and isonitrile ylides R2C-C≡N-R'. The identification of the highly reactive bisiminopropadienes 5 is supported by the observed shifts in the IR bands of the 15N and 13C isotopomers as well as theoretical calculations, tert-Butyl-substituted isoxazolones 7e and 7f, and 8i form the expected ketenimines 2, which then undergo elimination of isobutene and CO2 to generate C-cyanoketenimines 14 and 14i. N-Phenyl-dicyanoketenimine 32 is also described.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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