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  • Articles  (46)
  • Analytical Chemistry and Spectroscopy  (30)
  • Industrial Chemistry  (16)
  • 1965-1969  (46)
  • 1945-1949
  • 1968  (46)
  • 1
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The utility of benzoyl and pentadeuterobenzoyl derivatives of peptide methyl esters for mass spectrometric analysis was investigated. The mass spectra of the glu-his and the val-tyr-pro derivatives are discussed. Treatment of the peptide methyl esters with the mixed benzoic-ethyl-carbonic anhydride did in some cases lead to benzoyl derivatives as well as to ethoxycarbonyl derivatives.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 40 (1968), S. 910-914 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: In einem nicht stationär arbeitenden Laboratoriumsmodell eines Horizontalzersetzers wurde zunächst die Geschwindigkeitskonstante der Zersetzung an verschiedenen Graphit-Sorten gemessen. Aus den gewonnenen Daten und nach einer unter vereinfachender Voraussetzung aufgestellten Gleichung wurde die Graphit-Ausstattung eines technischen Horizontalzersetzers berechnet. Die danach ausgelegte Pile wurde in Dauerbetrieb erprobt.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1968), S. 169-187 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of guanidine and ten of its derivatives have been studied under both high and low resolution conditions. Evidence was detected for the migration of methyl groups, the formation of intermediate three-membered ring structures and decompositions involving expulsion of N. with release of kinetic energy.
    Additional Material: 13 Ill.
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  • 4
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of nine bridged polycyclic chlorinated pesticidal compounds have been investigated, and fragmentation modes to account for the more abundant ions are postulated. The principal features of the spectra are ions corresponding to a set of retro-Diels-Alder decompositions, ions resulting from successive losses of Cl, HCl, or both, ions produced by combinations of a retro-Diels-Alder process with a preliminary or subsequent loss of Cl or HCl, and ions whose processes of formation more specifically involve the epoxide group.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1968), S. 459-465 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of B substituted 2,5-dimethyl cyclotetrazenoboranes have been studied. The compounds Me2N4BD, Me2N4BEt, Me2N4BVi, Me2N4BCl and Me2N4BBr give confirmatory evidence that loss of N2+H. from the system occurs by loss of H from the side chain and that the B—R bond is very stable under electron impact conditions. Fragmentation proceeds in a similar fashion to that of the 2,5-dimethyl substituted compounds with H bonded to the boron atom.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1968), S. 713-737 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Fragmentation under electron impact of phenylhydrazones of aromatic aldehydes and ketones, of nitrostilbenes, nitrobenzalacetophenones and analogous compounds is determined by intramolecular oxidation reactions. Oxygen transfer from the o-nitrogroup on to the hydrazon- or stilbene-double bond is taking place; degradation of the resulting rearrangement products provides some of the most characteristic features in the mass spectra of such compounds. The spectra of 20 out of 40 compounds investigated are presented and discussed. Several other rearrangement reactions are observed. An additional conjugated double bond in the hydrazone chain completely changes the reactivity under electron impact. Even saturated substituents (cyclopropyl) can be drastically affected in their mode of fragmentation by an o-substituted nitrogroup.
    Notes: Die Fragmentierung von Nitrophenylhydrazonen aromatischer Aldehyde und Ketone, von Nitrostillbenen, Nitrobenzalacetophenonen und analogen Verbindungen unter Elektronenbeschuss wird entscheidend durch intramolekulare Oxidationsreaktionen beeinflusst, sofern sich eine Nitrogruppe in o-Stellung zum ungesättigten substituenten befindet. Es findet eine Sauerstoffübertragung von der o-Nitrogruppe auf die Hydrazon- oder Stilbendoppelbindung statt; ein wesentlicher Teil der charakterisierenden Fragmente in den Massenspektren dieser Verbindungen stammt aus dem Zerfall dieser Sauerstoffübertragungsprodukte. 20 Spektren von 40 untersuchten Verbindungen werden präsentiert und diskutiert. Eine Reihe weiterer umlagerungsreaktionen werden beobahtet. Eine konjugierte zusätzliche Dopplbindung in der Hydrazonkette ändert die Reaktivität der Verbindung vollsändig. auch die Fragmentierung gesättigter Substituenten (Cyclopropyl) kann durch eine o-Nitrogruppe entscheidend beeinflusst werden.
    Additional Material: 15 Ill.
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  • 7
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In comparing N-acetylmorpholine to closely related systems, two major differences in fragmentation are observed. M-15 and M-43 fragments, although quite common to such systems, are unusual with respect to their genesis. Formation of the M-15 fragment by loss of C-3 instead of the anticipitated loss of C-2 or C-8 is evident from shifts in the spectra of deuterated analogs. The M-43 species arises from total loss of the N-acyl substituent rather than the usual two-step loss of ketene plus a ring hydrogen. These data are presented in support of mechanistic rationale involving radical induced ring contraction to a common intermediate molecular ion. Techniques of high resolution mass spectrometry and isotope labeling have been employed to substantiate certain mechanistic details.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1968), S. 115-126 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of a series of metal complexes of dibenzoylmethane have been rationalized. The paths of novel rearrangement reactions involving both hydrogen and oxygen migration may differ according to the type of metal atom in the complex. Further examples are proposed of the effect of metal valency changes in ion reactions.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1968), S. 13-29 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of a variety of alkyl and aryl oxazoles have been determined and the spectra analyzed with the aid of deuterium labelling and high resolution mass spectrometry. In contrast to the corresponding benzenoid compounds, the mass spectra of isomeric alkyl oxazoles are distinctive and in this respect are akin to those of the corresponding pyridines. Further analogy to the pyridines is suggested by the unfavorable nature of a carbonium ion adjacent to the 2-position and this effect may be used to locate alkyl substituents attached to the oxazole nucleus. The loss of carbon monoxide from the molecular ions of 2,5-disubstituted oxazoles probably occurs with ring opening and migration of the C-5 substituent (e.g.Br) to the C-4 position.
    Additional Material: 12 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1968), S. 527-530 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using energetic considerations, ketonic structures are postulated for the [M—olefin]+ fragments derived from alkoxybenzenes, alkylthiobenzenes and 9-ethoxyanthracene. Experimentally determined heats of formation for the tautomeric molecular ions derived from anthrone and 9-anthrol differ by 37 Kcal. mole-1.
    Additional Material: 2 Tab.
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