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  • 1
    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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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 6 (1992), S. 667-670 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Radical-cations of iminopropadienones (RN=C=C=C=O+·) have been generated by dissociative ionization of isoxazle precursors a structurally characterized by collisional activation mass spectrometry; the corresponding neutral cumulenes have also been produced in a tandem mass spectrometer by neutralization and/or flash-vacuum pyrolysis experiments.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 6 (1992), S. 135-139 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Collisional Activation, charge-stripping and neutralization/reionozation mass spectra allow the identification of six [C6H7N]+· isomers, namely the molecular ions of the three isomeric picolines, 1+·-;3+·, ionized 2- and 4-methylene dihydropyridines, b - c, and ionized pyridinium methylide, a. The implication of the distonic forms a and b in some fragmentation reactions of funct of onalized (position 2) pyyridines is briefly discussed. Molecular orbital calculations indicate the b〉a〉1+· stability sequence.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 9 (1995), S. 795-799 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: An RF-only quadrupole collision cell, fitted with retardation and acceleration lenses, has been installed in a field-free region of a large-scale tandem mass spectrometer. This new arrangement has allowed decelerated, mass-selected ions (ca. 5 eV kinetic energy) to react with reagent gases and reaccelerated, mass-selected products (ca. 8 keV) to be subsequently identified by collisional activation mass spectrometry. The system was tested by looking at ion/molecule reactions of cyclobutanone molecular ions, previously studied by FTICR mass spectrormetry.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Heterocumulenes such as ketenes, propadienones and comulogs of isocyanates are produced by flash vacuum pyrolysis of Meldrum's acid. Real-time monitoring of the pyrolysis products is performed by methods of tandem mass spectrometry. In particular, chemical ionization is show, for the first time, to generate protonated moleculular ions of these kinetically unstable neutral molecules which can be identified by collisional activation experiments.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 8 (1994), S. 329-332 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Bis-aryliminopropadiene radical-cations, [ArN=C=C=C=NAr′]+·, have been generated by dissociative ionization of isoxazolopyrimidine precursors and structurally characterized by collisional activation mass spectrometry; the corresponding neutral cumulenes have also been produced in neutralization-reionization experiments.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A series of polycarbon sulfide radical cations, CnS+· (n = 2-6), have been detected in the 70 eV electron impact mass spectrum of benzothiazole. Application of collisional activation and neutralization-reionization mass spectrometry indicates their connectivity and the stability of the corresponding neutral molecules CnS in the gas phase. Closed shell HCnS+ ions (n = 2-6) and the corresponding radicals HCnS. have similarly been identified in the dilute gas phase of the mass spectrometer. The experimental results are supported by ab initio molecular orbital calculations at the QCISD(T)/6-311G** (based on additivity approximation) + ZPVE level.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    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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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 2 (1988), S. 176-179 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: C4H9O+ ions have been produced in the high pressure ion source of a triple sector mass spectrometer either by protonation of C4H8O isomers using methane as the reagent gas, or by methylation of C3H6O isomers using iodomethane or chloromethane as reagent gas. The collisional activation spectra of these mass selected C4H9O+ ions (m/z 73) allow the identification of several stable isomers in the gas phase.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 209-212 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Some sidechain rearrangements of N-propylbromotrizoles are studied by mass analysed ion kinetic enery and collision induced dissociation techniques. Loss of an allyl radical is shown to produce a protonated bromotriazole ion by double hydrogen transfer to the heterocyclie ring. Ethylene elimination gives rise to isomers of the methyl bromotriazole molecular ions. Finally, it is shown that no ring expansion occurs in the production of the [M-C2H5]+ ions.
    Notes: Quelques réactions de réarrangement faisant intervenir la chaîne latérale de N-propylbromotriazoles sont étudiées par les techniques ‘MIKE’ et ‘CID.’ La perte d'un radical allyle produit une structure bromotriazole protontée par double transfert d'hydroghe vers le noyau hétérocyclique. L'élimination d'ithylbéne donne naissance à des structures isoméres des ions moléculaires des méthylbromotriazoles. Enfin, les résultats montrent qu'il n'y a pas de réaction d'extension cyclique au niveau des ions [M—C2H5]+ de ces composés.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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