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  • 1970-1974  (2.417)
  • Analytical Chemistry and Spectroscopy  (2.128)
  • Physical Chemistry  (289)
Materialart
Erscheinungszeitraum
Jahr
  • 101
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. 175-178 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Upon electron-impact aryl methyl sulphones (I) rearranged to form aryl-oxygen bonds. The mode of fragmentation of the intermediate ester (II) to give [aryl O]+ or [aryl OH]+ ions was found to be markedly influenced by the nature of the aryl substituent.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 102
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. 11-23 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: A series of 3-acetoxy bicyclo[2.2.2]oct-2-ene 5,6 dicarboxylic anhydrides with different substituents is studied by high resolution mass spectrometry. The spectra obtained are complicated and can only be differentiated by the presence of certain peaks and their variable relative abundances. We have almost entirely explained these peaks by the use of classic degradation mechanisms. We have applied the explanations advanced by Cimarusti and Wolinsky for a series of analogues.The degradation scheme is very similar for all the products, and is unaffected by the substituents and their relative position.
    Notizen: Une série d'anhydrides du type acétoxy-3 bicyclo[2.2.2]octéne-2 dicarboxylique-5,6 ne différant que par des substituants hydrocarbonés, a été étudiée en spectrométrie de masse é I'aide de la haute résolution. Les spectres de cette série sont complexes et ne différent que par la présence de certains pics et par des intensités relatives variables. Par des mécanismes classiques, nous avons pu expliquer la presque totalité des pics. Nous nous sommes appuyés sur les mécanismes observés dans une série analogue1,2 de bicyclo-[2.2.2]octéne-2 étudiée par Cimarusti et Wolinsky. On retrouve le méme schéma directeur quels que soient les substituants et les positions relatives de ceux-ci.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 103
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The appearance potentials of [C9H9]+ have been estimated and the enthalpy of formation, calculated from the data, is correlated with different structural proposals. Open chain structures can be eliminated in favour of aromatic ones (vinyltropylium or indanyl cation). The structure of the unstable [C9H9]+ ions is investigated by means of 13C-labelled compounds. The results are also in agreement with the acceptance of aromatic structures.
    Notizen: Die Auftrittspotentiale von [C9H9]+ werden bestimmt und die baraus berechneten Bildungsenthalpien mit verschiedenen Strukturvorschlägen korreliert. Offenkettige Strukturen können in allen Fällen zugunsten von aromatischen (Vinyltropylium-,bzw. Indanylkation) aus-geschlossen werden. Die Struktur der instabilen [C9H9]+-Ionen wird mit Hilfe 13C-markierter Verbindungen untersucht. Auch hier stehen die Ergebnisse mit der Annahme aromatischer Strukturen im Einklang.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 104
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. 49-60 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The CH4 chemical ionization (CI) spectra of several keto-steroids are reported as well as the H2 and C3H8CI spectra of a few keto-steroids. [M + H — H2O]+ is an abundant ion in the CH4CI spectrum of 5α-androstane-17-one and the water loss from the [M + H]+ ions does not involve the hydrogens on C-18 and only involves the C-16 hydrogens to about 10%. The major loss process has not been determined.3-Keto and 17-Keto steroids are readily distinguished by their CH4CI spectra. The effectiveness of substituents for directing attack by [CH5]+ and [C2H5]+ can be estimated:carboxyl 〉 methoxy ≃ carbonyl 〉 bromo ≃ chloro 〉 hydroxy. Significant differences are observed in the H2CI spectra of two 5α-vs. 5β-steroids. Propane CI Spectra are similar to methane CI spectra, but show generally less fragmentation.
    Zusätzliches Material: 5 Tab.
    Materialart: Digitale Medien
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  • 105
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. 81-83 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The heats and entropies of gas phase association of chloride, bromide and iodide with the respective methyl halides are reported. Comparison of these results with results published for SN2 reactions in solution suggests that the solvent is the dominant factor in determining relative halide nucleophilicities for the reactions in solution.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 106
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. 109-115 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectra of three series of stereoisomeric 3-aza-3-methyl-6-cycloalkylaminobicyclo[3,3,1]nonan-9-ols and related compounds including deaza analogues are reported and discussed. The spectra of some of the isomers differ characteristically and can be used to assign their configurations.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 107
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. 257-266 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The electron ionization mass spectra of the trimethylsilyl derivatives of a number of medicinal barbiturates have been examined. The trimethylsilyl derivatives are useful in the identification of barbiturates by gas liquid chromatography/mass spectrometry (g.l.c.-m.s.). Mass spectra of these derivatives are characterized by abundant high mass ions which permit the ready distinction of one barbiturate from another. The prominent and characteristic [M - 15] ion is an effective monitor of molecular weight, while other unique fragmentations and/or varying patterns of relative abundance serve to differentiate isomers.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 108
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. i 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 109
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Different methods have been tested to determine the activation energy for simple cleavages.
    Notizen: L'énergie d'actvation des ruptures simples a été determiné par différents méthodes.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 110
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 19-30 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Mass spectra of substituted phenoxazines and azaphenoxazines have been determined and are discussed here. These compounds are characterised by hydrogen on the heterocyclic nitrogen and aromatic rings with nitro groups and chlorine as substituents. The fragmentation patterns are explained by known mechanisms. An interpretation of almost all the peaks is offered. The presence of the substituents causes a complete change in the fragmentation patterns compared with the unsubstituted phenoxazine. This is due to changes in charge localisation, caused by the substituents. Isomerisation of the nitro group to the nitroso group gives rise to a particular fragmentation route.
    Notizen: Nous avons effectué les spectres de masse de phénoxazines et d'azaphénoxazines substituées. Ces composés sont caractérisés par la présence d' un hydrogéne sur l'azote hétérocyclique et la position de substituants NO2 et Cl sur les cycles aromatiques. A l'aide de mécanismes classiques, nous avons rationalisé les processus de fragmentation et expliqué les pics principaux de ces specters. La présence de substituants Cl et NO2 perturbent totalement la fragmentation observée dans le cas de la molécule de phénoxazine. Ils favorisent la localisation de la charge suivant leur position sur le cycle, soit sur l'azote, soit sur l'oxygéne hétérocycliques. Quant au gropement NO2 par isomérisation (forme nitroso), il donne lieu éa une fragmentation spécifique.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 111
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Mass spectra obtained from the three title compounds were compared. High resolution studies and deuterium labelling allowed a proposal for an original cracking pattern, typical of the structure. The postulated mechanism involves a six-centred cyclic electron transfer, generating an aromatic radical ion. Cracking patterns characteristic of barbiturates could also be observed.
    Notizen: Les spectes de masse de ces trois composés ont éteacute; comparé. L'utilisation de la haute résolution et de la méthode de marquage au deuté a permis de mettre en évidence un mécanisme de fragmentation particulier commun aux trois dérivés. Ce mécanisme consiste en un transfert électronique cyclique á six centres donnant naissance á un ion radical aromatique. Les mécanismes de fragmentation propres aux barbituriques ont également été observé.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 112
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. i 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 113
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The fragmentation mechanisms of the title compound upon impact with 70 and 12 eV electrons has been studied using specific trideuteriomethyl derivatives. By application of the proposed fragmentation mechanisms, the number as well as the location of methyl groups in all theoretically possible methyl derivatives of methyl D-glucopyranos duronic acid unequivocally can be determined after exhaustive trideuteriomethylation. For this purpose low energy (12 eV) spectra are recommended, as these contain only the structurally significant ions.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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  • 114
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 204-210 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: An aspect of the mechanism of the hydroxyl H/ortho H scrambling in the molecular ion of benzoic acid was studied by the open-shell INDO molecular orbital method. Energies of te unrearranged structure, the planar structure in which H is attached to carbonyl oxygen and rotational conformers of the latter were studied to determine a pathway of minimum energy for rotation. The same calculations were made for salicylic acid, m-fluorobenzoic acid and p-fluorobenzoic acid. The results of these calculations agree quite well with experimental results.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 115
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 189-194 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The metastable ion supported fragmentation process in the mass spectra of the cyclohexadienyl derivative C6H7Mn(CO)3, the cycloheptadienyl derivative C7H9Mn(CO)3, the 1,2,3,4,5-and 1,2,3,5,6-pentahaptocyclootadienyl derivatives C8H11Mn(CO)3, the cyclooctatrienyl derivative C8H9Mn(CO)3 and the substituted cyclopentadienyl derivative (CH3)2NCH2C5H4Mn(CO)3, are described. Losses of carbonyl groups, generally stepwise, from the molecular ions to give the corresponding [M - 3CO]+· ions are first observed. Further fragmentation of the carbonyl-free [M - 3CO]+· ions can involve a variety of processes such as the following: (a) elimination of a neutral manganese atom to give a hydrocarbon fragment; (b) elimination of a neutral hydrocarbon fragment to give an [MnH]+· ion; (c) dehydrogenation; (d) elimination of a 2-carbon C2H2 or C2H4 fragment; (e) elimination of a C3H4 or C3H6 fragment as a neutral species when it is bridging two carbon atoms bonded to manganese, as in C8H9Mn(CO)3 and 1,2,3,4,5,h5-C8H11Mn(CO)3, respectively. Fragmentation of the [M - 3CO]+· ion in (CH3)2NCH2C5H4Mn(CO)3 presents the following additional features: (a) elimination of C6H6 with a nitrogen shift from carbon to manganese; (b) elimination of a neutral dimethylamino fragment to give [C6H6Mn]+·, which then loses neutral C6H6, C6H5 or Mn fragments and thus is formulated tentatively as [(fulvene)Mn]+· or [C6H5MnH]+· rather than [(benzene)Mn]+·.
    Materialart: Digitale Medien
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  • 116
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 195-203 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1,2-Diaminoethane and 2-aminoethanol-1 were added to the isobutane plasma of a chemical ionization mass spectrometer. The resulting reactant gas mixture did not react with additives containing a single oxygen functional group. Addition reactions were observed with some additives containing multiple oxygen functions. Additives containing nitrogen functions were protonated by the reactant mixture. The relative proportion of protonation to addition depended on the ability of the additive to chelate the reactant ion and on the basicity of the additive. This use of 1,2-diaminoethane and 2-aminoethanol-1 provides a convenient method of varying the reactivity of the plasma in a chemical ionization source.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 117
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 1052-1054 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The ionisation potentials of pyridines substituted with electron-donating and electron-withdrawing substituents in positions 2, 3 and 4 have been determined.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 118
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Collisional activation spectra show that the [C9H11O] ion formed by loss of CH2OH from the title compound has rearranged to the protonated phenylacetone structure.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 119
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 998-1005 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Ionisation potentials of benzophenone and nine substituted benzophenones, and appearance potentials of the most abundant fragment ions have been determined. Starting from calculated heats of formation of the substituted benzophenones, the following quantities have been evaluated; heats of formation of the molecular ions; heats of formation of fragment ions formed via a one-step pathway and via a two-step pathway; heats of formation and ionisation potentials of radicals; heats of dissociation of benzophenone and substituted benzophenones. The accuracy of the result is discussed.
    Notizen: Es wurden die Ionisieerungspotentiate von Benzophenon und substituierten Benzophenonen sowie die Auftrittspotentiale der häufigsten Fragment-Ionen gemessen. Ausgehend von berechneten Werten für die Bildungsenthalpien der substituierten Benzophenone, wurden folgende Grüßen ermittelt: Bildungsenthalpien der Molekül-Ionen; Bildungsenthalpien von Fragment-Ionen, die in einem einstufigen, und solcher, die in einem zweistufigen Zerfallsprozeß gebildet wurden; Bildungsenthalpien und Ionisierungspotentiale von Radikalen; Dissoziationsenergien des Benzophenons und der substituierten Benzophenone. Die Genauigkeit der Ergebnisse wird diskutiert.
    Zusätzliches Material: 8 Tab.
    Materialart: Digitale Medien
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  • 120
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The process of retro-1,3-dipolar cycloaddition of 2,5-diaryl-1,3,4-dioxazoles induced by electron-impact is discussed. For this purpose, 2-phenyl-5-p-chlorophenyl-1,3,4-dioxazole was prepared, labelled with 18O in position 1; the spectrum of this compound showed clear evidence of retro-cycloaddition, the dipole fragment retaining the positive charge. This labelled compound also provides a reliable interpretation of other cleavage modes of the heterocyclic ring. The elemental compositions of the ions considered were determined by exact mass measurements and the metastable transitions were detected through the defocusing technique of the electrostatic sector.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 121
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectra of TMS ethers of 2,3,-dialkyl-1,4-cyclopentanediols having a 2′-carboxyl group or 2′-double bond in one of the sidechains, display a stereospecific rearrangement process. A mechanism is proposed to account for this stereospecificity.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 122
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 257-263 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: It is shown by D labelling experiments that nitrous acid and hydroxyl, eliminated from the methyl ester of γ-nitrobutyric acid upon electron-impact, contain a γ-hydrogen atom to the extent of ∼ 85% and ∼ 100%, respectively. The loss of nitrous acid is the third case of a highly specific 1,1-elimination from a molecular ion1a,1b reported hitherto and arguments are presented for the essential role played by carbomethoxy group in this reaction, i.e. it converts the nitro structure of the molecular ion to its acinitro structure. The results obtained further point to a stepwise character of the McLafferty rearrangement, at least for the present case.
    Zusätzliches Material: 1 Ill.
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  • 123
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The mass spectrometric fragmentations of ethylene ketals corresponding to α substituted ketones were re-examined. A new type of rearrangement has been established.
    Notizen: La fragmentation des éthylénecétals des cétones α substituées a été étudiée. Un nou-veau type de transposition en spectrométrie de masse a été mis en évidence.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 124
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The differences in the electron-impact-induced fragmentation of ortho and para- nitrobenzoylpiperidine are connected with neighbouring group participation of the NO2 group. New oxygen migration, as well as the formation of stabilised radicals by intramolecular interaction of both functions, are only possible with the ortho compound.
    Notizen: Die Unterschiede bei der elektronenstoßinduzierten Fragmentierung von ortho-und para-Nitrobenzoylpiperidin hängen mit einer Nachbargruppenbeteiligung der NO2,-Gruppe zusammen. Sowohl eine neuartige Sauerstoffwanderung als auch die Ausbildung stabilisierter Radikale über eine intramolekulare Wechselwirkung der beiden Funktionen sind nur bei der ortho-Verbindung möglich.
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  • 125
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 265-273 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The structure and decomposition of the [C7H7]+ ions produced by electron-impact from o-, m- and p-chlorotoluene, o-, m- and p-bromotoluence, and p-iodotoluence, have been investigated. By determining the relative abundance of normal and metastable ions, these [C7H7]+ ions at electron energy of 20 eV are shown to be so-called ‘tropylium ions’. The amount of the internal energy of the [C7H7]+ ion estimated by the relative ion abundance ratios, † [C5H5]+/[C7H7]+ and m*/[C7H7]+ for the decomposition \documentclass{article}\pagestyle{empty}\begin{document}$ [{\rm C}_{\rm 7} {\rm H}_{\rm 7}]^ + \mathop \to \limits^{m^* } [{\rm C}_{\rm 5} {\rm H}_{\rm 5}]^ + + {\rm C}_{\rm 2} {\rm H}_{\rm 2} $\end{document}, is in the order iodotoluene 〉 bromotoluene 〉 chlorotoluene. The heats of formation of the activated complexes for the reaction \documentclass{article}\pagestyle{empty}\begin{document}$ [{\rm C}_{\rm 7} {\rm H}_{\rm 7}]^ + \mathop \to \limits^{m^* } [{\rm C}_{\rm 5} {\rm H}_{\rm 5}]^ + + {\rm C}_{\rm 2} {\rm H}_{\rm 2} $\end{document} were estimated. The values suggest that the decomposing [C7H7]+ ions from various halogenotoluenes are identical in structure.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 126
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: By the investigation of 2H labelled compounds, it has been established that in the case of crotonoyl piperidyl only the hydrogens of the methyl group participate in the elimination of CH3·.
    Notizen: Durch die Untersuchung 2H-markierter Verbindungen wird belegt, daß im Falle von Crotonsäurepiperidid nur die Wasserstoffe der Methylgruppe an der CH3·-Abspaltung teilnehmen.
    Zusätzliches Material: 1 Tab.
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  • 127
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 289-296 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectra of five B,B′-disubstituted derivatives of the bis(amino)diboranes(4). Most of the fragmentations postulated have a precedent in similar processes of isoelectronic and/or isopolar species and are supported by the occurrence of metastable peaks.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 128
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 304-309 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Fragmentations of the carboxyl group are not generally observed from molecular anions produced by the capture of slow electrons. Enhancement of the internal energy of the molecular anions by collision excitation allows the detection of the fragmentations of the substituent in the field free regions of the mass spectrometer. Fragmentations include the losses of CO2 or ·CO2H from molecular anions, and the elimination of CO2 from fragment ions.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 129
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The structure of stable [C9H11]+ ions from different model compounds with the molecular formula C9H11Cl has been estimated by energy measurements. It has further been shown that acetylenic compounds cyclise to form aromatic ions in the range of the appearance potentials.
    Notizen: Die Struktur der stabilen [C9H11]+-Ionen aus verschiedenen Modellverbindungen der Summenformel C9H11Cl wird mit Hilfe energetischer Messungen untersucht. Es wird ferner gezeigt, daß Acetylenverbindungen im Bereich der Auftrittspotentiale zu aromatischen Ionen cyclisieren.
    Zusätzliches Material: 2 Tab.
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  • 130
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 310-320 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Linear plots may be obtained for the fragmentations of aryl p-cyanobenzoates using the McLafferty approach, but the correlations are not as satisfactory as those observed1 for aryl nitrobenzoates. Some satisfactory correlations of substituent effects are noted in the negative ion spectra of substituted benzyl-p-nitrobenzoates and substituted phenyl-(p-nitrophenyl)acetates. Pronounced rearrangement peaks are observed in the spectra of substituted phenyl-(p-nitrophenyl)acetates. Appearance potential studies suggest that the similarities in ρ values obtained1 for the fragmentations of aryl m- and p-nitrobenzoate molecular anions are probably due to the correspondence between Hammett σ values and appearance potentials in the two series.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 131
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Under electron-impact [C7H7]+ ions from open chain compounds only partially isomerise to a tropylium ion. The extent of this process depends on the life time τ and the internal energy E.
    Notizen: [C7H7]+-Ionen aus offenkettigen Verbindungen isomerisieren unter Elektronen-stoss nur partiell zu einem Tropylium-Ion, wobei die Lebensdauer τ bzw. die innere Energie E das Ausmass der Cyclisierung bestimmt.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 132
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The enthalpy of formation of stable ions of some C8H6, C10H10 and C12H10 hydrocarbons have been calculated by means of AP/IP measurements and their correlation with thermochemical data. It has further been shown that under electron-impact-induced fragmentation aromatic and isomeric acetylenic compounds give open chain as well as cyclic ion structures.
    Notizen: Mit Hilfe von AP/IP-Messungen und deren Korrelation mit thermochemischen Daten werden die Bildungsenthalpien stabiler Ionen einiger C8H6-, C10H10 und C12H10-Kohlen-wasserstoffe bestimmt. Es wird gezeigt, dass sowohl offenkettige als auch cyclische Ionen-Strukturen bei der elektronenstossinduzierten Fragmentierung von Aromaten und isomeren Acetylenverbindungen ausgebildet werden können.
    Zusätzliches Material: 4 Tab.
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  • 133
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 335-342 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectra of 4-(ω-hydroxyalkylamino)-phthalazinone derivatives (I to IV) have been studied. The most important primary fragmentation process is the fission of the alkyl chain β to the amino group, combined with an intramolecular cyclisation reaction. This process results an ion of tricyclic structure, possessing a 4-membered ring, as was established by partial 15N labelling.
    Zusätzliches Material: 1 Tab.
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  • 134
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 343-345 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The mechanism of methyl elimination has been investigated with the help of 13C-labelled p-methylstyrene. Not only terminal C atoms participate in this process; however, neither complete nor partial C scrambling ensues prior to the fragmentation.
    Notizen: Mit Hilfe 13C-markiertem p-Methylstyrol wird der Mechanismus der Methyl-Abspaltung untersucht. An diesem Prozeß sind nicht nur endständige C-Atome beteiligt, jedoch erfolgt weder ein vollständiges noch ein partielles C-Scrambling vor der Fragmentierung.
    Zusätzliches Material: 1 Tab.
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  • 135
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 346-349 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The principal fragmentation pathways of mevalonolactone are initiated by cleavage α to the hydroxyl function. Each major route has been delineated by using isotopic labelling and metastable analysis. A knowledge of this fragmentation pattern is useful for the calculation of isotopic purity and specificity in samples of mevalonolactone used as substrates in biosynthetic studies.
    Zusätzliches Material: 1 Tab.
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  • 136
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 350-358 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The ionisation potentials and characteristic fragmentations of a series of anilinium oxides and their isomeric ethers have been used to assign structures for the gaseous species from the zwitterions. Transmethylation and direct evaporation of the zwitterions are competing processes. A bulky substituent ortho to the oxygen or a strongly electron attracting group in the 2-isomer will prevent or reduce the transmethylation. If the volatility is much reduced, however, the temperature increase for evaporation results in transmethylation. The 4-isomer was transmethylated even with two tert-butyl groups ortho to the oxygen. The appearance potentials for an isomeric pair showed the energy difference between the zwitterion and the ether in the gas phase to be 11.5 kcal/mol.
    Zusätzliches Material: 2 Tab.
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  • 137
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 365-371 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Independent loss of positional identity of the hydrogen and carbon atoms in [t-C3H8N]+ metastable cations prior to fragmentation in the gas phase with loss of ethylene, has been demonstrated by 2H and 13C labelling experiments. The scrambling reaction is interpreted as a rearrangement in competition with the high activation energy unimolecular decompositions. The study of this fragmentation process indicates the occurrence of a primary isotope effect discriminating in favour of 2H and 13C retention in the original methylene group.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 138
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 372-394 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Diterpene epimers differing with respect to orientation of a secondary hydroxyl group, ring fusion or configuration at an asymmetric centre carrying carbon-carbon linked substituents were studied, and certain stereostructural-spectral correlations were achieved for the first two groups. Each of the compounds examined was subjected to multiple scanning at both high and low electron voltage to allow computer assisted statistical calculation and comparison of intensity intervals at a predetermined confidence level for total ion currents and selected peaks.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 139
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 418-421 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: When subjected to electron-impact, chloromethyl aryl sulphones (II, X = Cl) fragment predominantly by the loss of CH2Cl from the molecular ion followed by the loss of SO2 and in most cases the appropriate metastable peaks are present to confirm the transitions. In addition, alkyl-oxygen bond formation in the molecular ion was revealed by the presence of prominent peaks corresponding to the [R—φ-SO]+ ions. In most spectra no evidence for aryl-oxygen bond formation could be found and thus the presence of the chlorine atom was able to effectively reverse the direction of skeletal rearrangement reported for aryl methyl sulphones.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 140
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The effect of the dissociation energy of the C—X bond (X = H, F, Cl, Br, I) on the formation of benzimidazolium ions (b) by elimination of X from the molecular ions of ortho-substituted N,N-dimethyl-N′-phenylformamidines (I to V) has been investigated. No simple relation is observed between the intensities of ions b and the dissociation energy. Furthermore, the appearance potentials of ions b are not greatly affected by the dissociation energy, although differences of about 2.5 eV are expected for a simple cleavage reaction. The behaviour of the molecular ions of I to V is in accord with a two step addition-dissociation mechanism [M]+· → a → b, and the highest activation energy is required in the first addition step. Similar mechanisms are known for aromatic substitution reactions in the condensed phase, but have not been observed for mass spectrometric fragmentations. The detection of additional kinetic energy T in the reaction products by an analysis of the metastable transitions [M]+· → b corroborates the proposed mechanism.
    Notizen: Der Einfluß der Dissoziationsenergie der C—X-Bindung (X = H, F, Cl, Br, J) auf die Bildung von Benzimidazolium-Ionen (b) durch Abspaltung von X aus den Molekül-Ionen der ortho-substituierten N,N-Dimethyl-N′-phenylformamidinen (I bis V) wird untersucht. Zwischen den Intensitäten von b und den Dissoziationsenergien besteht keine einfache Beziehung. Weiterhin werden die Auftrittspotentiale der lonen b nur wenig von den Dissoziationsenergien beeinflußt, obwohl fur eine einfache Spaltungsreaktion Unterschiede von ca. 2.5 eV erwartet werden. Dieses Verhalten der Molekül-Ionen von I bis V steht irn Einklang mit einem zweistufigen Additions-Dissoziations-Mechanismus [M]+· → a → b, bei dem der erste Additionsschritt die hohere Aktivierungsenergie besitzt. Analoge Mechanismen sind bei aromatischen Substitutionen in kondensierter Phase bekannt, für massenspektrometrische Fragmentierungen bisher jedoch noch nicht nachgewiesen worden. Der Nachweis zusätzlicher kinetischer Energie T in den Reaktionsprodukten mit Hilfe einer Analyse der metastabilen Übergange für [M]+· → b bestätigt den vorgeschlagenen Mechanismus.
    Zusätzliches Material: 3 Tab.
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  • 141
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 422-434 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The electron-impact mass spectra of a range of N-substituted sulphoximines have been recorded and rationalised. Intense peaks consistent with oxygen-to-sulphur and sulphur-to-sulphur migrations were observed in the spectra of some of the compounds.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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  • 142
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 435-442 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: We have synthesised all the fluorinated derivatives of perchloropyrimidine, trichloro-2,4,6-pyrimidine and perchloro-s-triazine. Fluorine n.m.r. analysis, associated with gas chromatography coupled with mass spectrometry, allowed separation and identification of the products. The behaviour of these compounds under electron-impact is presented and discussed here.
    Notizen: Nous avons synthétisé tous les dérivés fluorés de la perchloropynmidme, de la 2,4,6 trichloropyrimidine et de la perchloro s-triazine. La r.m.n. du fluor associée au couplage chromatographie en phase vapeur-spectrométrie de masse, nous ont permis de séparer et d'identifier les produits obtenus. Nous presentons et discutons le comportement de ces composes sous l'impact électronique.
    Zusätzliches Material: 9 Ill.
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  • 143
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 510-513 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The electron-impact-induced fragmentation of a 13C labelled exo-2-norbornyl chloride has been studied. When the norbornyl cation, [C7H11]+, [M - Cl], dissociates by elimination of C2H4, carbon atoms are randomly lost showing that extensive skeletal rearrangement (in addition to the complete hydrogen atom scrambling reported earlier) has taken place in the norbornyl cation prior to dissociation.The metastable ion peak associated with the above fragmentation consists of superimposed gaussian and flat-top components; it is proposed that these correspond to the formation of isomeric [C5H7]+ daughter ions whose heats of formation differ by ∼0.4 eV.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 144
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 536-547 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A method is reported for the identification of trimethylsilylated stereoisomeric N-acetyl-hexosamines by application of a pattern recognition procedure to mass spectral data. The selection of characteristic mass spectral data and the pattern recognition procedure are discussed.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 145
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 582-584 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Electron-impact studies of diazadiphosphetidines,[YF2PNMe]2(Y—F,Me, Ph, MeO,2,5-Me2C6H3, and m-CF3C6H4) are reported, the most abundant fragments corresponding to m/e [M/2-1]+, [M/2]+ and [M/2-1]+. It is concluded from metastable data that formation of the noval rearrangement ion, [M]+→[M/2+1]+is predominantly due to an electron-impact process. Variable temperature spectra of(F3PNMe)2, (i.e. for Y=F), suggest that ions of m/e [M/2-1]+are formed, in part, by a thermal process. For the compound [(m-CF3C6H4)F2PNMe]2 a well resolved negative ion spectrum has been obtained, with the molecular ion present in 100% abundance.
    Zusätzliches Material: 3 Tab.
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  • 146
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The structures of ions produced from acyclic 1,3-diketones by loss of carbon monoxide, ketene or olefins are investigated. Structural inference is made by comparison of the heats of formation of these ions with data for ions of known structure generated from other precursors. All assignments are confirmed by a study of metastable transitions. Loss of carbon monoxide yields ions in the keto form. Expulsion of a ketene or olefin moiety results in enol type ions.
    Zusätzliches Material: 7 Tab.
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  • 147
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 594-600 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Mass spectra of closo-phosphorimide, P4(NCH3)6, closo-thiophorimides, P4(NCH3)6Sn with n ranging from 1 to 4 and closo-arsenimide As4(NCH3)6 were obtained, and systematic trends were recognised in their fragmentation patterns. The introduction of thiophosphoryl groups gives a superposition of the fragmentation modes indentified with P4(NCH3)6 and P4(NCH3)6Sn. The fragmentation paths are completely different from those of adamantane and its derivatives or hexamethylene teramimne.
    Notizen: Les spectres de masse du closo phosphorimide P4(NCH3)6Sn, où n = 1 à 4, et du closo arsenimide As4(NCH3)6 ont été et des schémas de fragmentations systématiques ont été dégagés, L'introduction des groupes thiophosphoryles se traduit par une superposition des deux types de fragmentations identifiées pour P4(NCH3)6 P4- dérivés ou de l'hexaméthylène tétramine.
    Zusätzliches Material: 1 Ill.
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  • 148
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 601-608 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The major reactions of aryl substituted N-t-butylbenzamides upon electron-impact involve direct cleavage of a methyl radical, the loss of a butene molecule with the transfer of one hydrogen, or the loss of a butenyl radical with the transfer of two hydrogens. The last of these processes parallels the mass spectral behavior of aliphatic amides. Substituent effects indicate that electron-withdrawing groups on the aromatic ring enhance the two hydrogen transfer process, while electron-donating groups enhance the single hydrogen transfer process. Ion abundances, ionization potentials and appearance potentials are discussed with respect to correlation with σ+ values.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 149
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: During the fragmentation of thiaspirofuranone under electron-impact a process is presumed to occur that is best rationalised as a ring contraction of the neutral particle C6H10. A carbene structure for this neutral fragment can be excluded.
    Notizen: Bei der elektronenstoßinduzierten Fragmentierung des Thia-spirofuranons findet ein Prozeß statt, der am besten durch die Annahme einer Ringkontraktion des Neutralteiles C6H10 rationalisierbar ist. Eine Carben-Struktur für dieses Neutralteil kann ausgeschlossen werden.
    Zusätzliches Material: 1 Tab.
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  • 150
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 622-625 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: In the formation of the [M-l]+ ions from phenylsilanes an isotope effect i is observed as well as a preference factor p. The formation of intense [M-2]+ and [M-3]+ ions is compatible with the performance of open chain systems. A decision for or against the structure of a silatropylium ion is not possible by the investigation of 2H labelled compounds.
    Notizen: Bei der Bildung der [M — H]+-Ionen aus Phenylsilan wird sowohl ein Isotopeneffekt i als auch ein Präferenzfaktor p beobachtet. Die Entstehung intensiver [M - 2]+- und [M - 3]+-Ionen ist mit der Vorstellung offenkettiger Systeme verträglich. Eine Entscheidung für oder gegen die Struktur eines Silatropylium-Ions ist durch die Untersuchung 2H-markierter Verbindungen nicht möglich.
    Zusätzliches Material: 1 Tab.
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  • 151
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 628-630 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectra of hydrocinnamaldehydes, labelled with 13C in Position 1 and 3, have been studied in order to determine the origins of the carbon atoms in the moieties C2H2O, C3H4O, CH3 and CO, expelled from the molecular ion.
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  • 152
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974) 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 153
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 626-627 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Three empirical equation which have been used to calculate ionisation potentials of para and meta disubstituted benzenes are evalyated according to their ability to predict the IP's of para and meta YC6H4COX, (where x — OH, NH2, CL).
    Materialart: Digitale Medien
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  • 154
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 631-633 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Trimethylsilyl derivatives of 5′-S-alkyl substituted 5′-thioadenosines give mass spectra that are characterized by a number of highly intense ions. These ions are formed by the fragmentation of the alkyl substituted sugar moicty and are specific for the alkyl group in the substitution.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 155
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. i 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 156
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 660-664 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: During the fragmentation of 1.3-dioxoles by electron-impact an aryl rearrangement of the electrophilic as well as of the nucleophilic function occurs. Moreover, in one case a cleavage of geminal bonds at the spiro carbon is observed, which can be explained by the product stability of the doubly charged ion.
    Notizen: Bei der elektronenstroßinduzierten Fragmentierung 1.3-Dioxolen werden im Gegensatz zu sonstigen Arylwanderungen sowohl die nucleophile als auch die elektrophile Gruppe umgelagert. Anßerdem wird in einem Fall eine ungewöhnlich intensive Spaltung geminaler Bindungen am Spiro-Kohlenstoff beobachtet, die durch die Produkt-Stabilität des doppelt geladenen Fragment-Ions erklärbar ist.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 157
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The structures of kikumycin A and B, antiviral amidine antibiotics, have been elucidated by means of low and high resolution mass spectrometry. Amino acid composition and their sequences were also clearly demonstrated by this technique. The evidence for the fragmentation of terminal amidines or amides of kikumycin derivatives and related synthetic compounds was represented by the elimination of ammonia or water from the molecular ions to give stable nitrile ions. Additionally, the participation of the iminol structure in the pyrrole-2-carboxamide portion of kikumycin A and B was confirmed by the fragment ions derived from their iminol tautomers.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 158
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 649-659 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectral fragmentation of seven substituted 2,4,6-triaryl-s-trithianes has been studied and the fragmentation modes confirmed by deuterium labelling. Triphenyl-s-trithiane shows some interesting features in its mode of cleavage and does not eliminate S, S2, SH·, H2S or S2H· from its molecular ion. The prominent radical ions in the mass spectrum are at m/e 180 (52.3%) and m/e 186 (45.2%), corresponding to stilbene and PhCHS3. Their compositions have been established by deuterium labelling and accurate mass measurements. The formation of stilbene indicates a relationship between pyrolytic and electron-impact studies. The origin of [PhCHS3]+· suggests that one of the sulphur atoms attaches itself to the other two sulphur atoms in the molecular ion, eliminating a stilbene radical ion. The other important fragmentation corresponds to the monomer radical ion (thiobenzaldehyde) and the thiobenzoyl cation.Among the other substituted triaryl-s-trithianes with substituents such as chloro, methoxy, methylenedioxy and hydroxy groups on the phenyl ring (IV to IX), only the tris-(p-chlorophenyl)-s trithiane shows an insignificant molecular ion. Unlike the triphenyl derivative, the chloro, methoxy and methylenedioxy derivatives show the loss of HS· and/or H2S from the molecular ion. The spectrum of tris-(p-hydroxyphenyl)-s-trithiane corresponds to the spectrum of p-hydroxythiobenzaldehyde.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 159
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The electron-impact-induced fragmentation of some 1-thiacycloalkanones and their 1, 1-dioxides of ring size 5 to 8 was studied. The results were compared with the fragmentation pattern of the cycloalkanones, the thiacycloalkanes and the 1-thiacycloalkan-1, 1-dioxides. It was found that in thiacycloalkanones the charge localisation predominates at the sulphur.
    Notizen: Die elektronenstoßinduzierte Fragmentierung einer Reihe von 1-Thiacycloalkanonen und 1-Thiacycloalkanon-1.1-dioxiden mit 5 bis 8 Ringgliedern wurde untersucht. Die Ergebnisse wurden mit denen des Fragmentierungsverlaufes in den Cycloalkanonen, in den Thiacycloalkanen und in den 1-Thiacycloalkan-1.1-dioxiden verglichen. Es Zeigte sich, daß in den Thiacycloalkanonen der bevorzugte Ort der Ladungslokalisierung der Schwefel ist.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 160
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 672-678 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectrometric behaviour of six simple α-aminooxy acids is described. Comparison is made with the electron-impact-induced fragmentation of the parent α-amino acids. The differences are in accordance with the observedSee Ref. 1. chemical character of the α-aminooxy acids.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 161
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 679-685 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The principal fragmentation of the cis-β-methoxystyrene molecular ion is loss of the methyl group. Although this compound has a π system similar to that of phenyl acetate, the substituent effect of a strongly electronegative ortho substituent is insignificant for this fragmentation; but for the same substitution in phenyl acetate, it had been shown to be important. The INDO method was used to show that bond orders confirm the lack of the substituent effect in the cis-β-methoxystyrene system.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 162
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: An automated system is described for computer examination of the mass spectrum of an unknown mixture for the presence of a specific compound. The probability that the compound is present is indicated as a ‘confidence index’ K; 2K should signify the average number of compounds, selected at random, whose mass spectra would have to be examined to find data which match the target spectrum to the same degree as does the unknown. The value of K is determined by the uniqueness U of the m/e value, the abundance A, and the criterion of abundance agreement W of the matching peaks, and of the compound concentration D in the sample. Application to spectra from a variety of compounds, including illicit drugs, indicates that the system has high sensitivity and selectivity, and that the value of K is a useful index of the reliability of the identification. Initial testing of this system has utilized an automated quadrupole mass spectrometer under control of a dedicated microcomputer with sample introduction through a flash evaporator and membrane separator.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 163
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The existence of 5- or 6-membered cyclic bromonium ions, produced from ω-phenyl alkyl bromides under electron-impact conditions, is decisively dependent upon the stability of the phenyl alkyl radicals.
    Notizen: Die Existenz von füntf- oder sechsgliedrigen cyclischen Bromonium-Ionen, die aus ω-Phenyl-alkylbromiden unter Elektronenstoßbendingungen erzeugt werden, hängt in entscheidender Weise von der Stabilität der Phenyl-Alkyl-Radikale ab.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 164
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The electron-impact-induced fragmentation of piperidides from β-substituted α, β-unsaturated carboxylic acids proceeds preferentially via 4-membered cyclic transition states. The development of a 6-membered ring, which is typical for α,β-unsaturated esters, occurs only to a minor extent. The mechanism of the reaction is best rationalised by the assumption of a vinylogous α-cleavage and a simultaneous neighbouring group participation of the amide function
    Notizen: Piperidide von β-substituierten α,β-ungesättigten Carbonsäuren fragmentieren unter Elektronenstoßbedingungen hevorzugt über viergliedrige Übergangszustände. Die für α,β-ungesättigte Carbonsäureester typische Ausbildung von Sechsringsystemen findet nur untergeordnet statt. Der Mechanismus der Reaktion ist am besten rationalisierbar durch die Annahme einer vinylogen α-Spaltung und gleichzeitiger Nachbargruppenbeteiligung der Amidfunktion.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 165
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 710-713 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 2-Methoxy-8,9-dehydroadamantane and 2-exo-methoxyprotoadamantene undergo common electron-impact fragmentations at 70, 20 and 14.3 eV.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 166
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974) 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 167
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 726-729 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The presence of a 2′-tertiary hydrogen atom has a profound influence on the general fragmentation pattern of 4,6-dialkyl-1,3-dioxanes. Branching at the 2′-position induces a double hydrogen transfer reaction which is absent in the spectra of 4,6-n-alkyl-1,3-dioxanes.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 168
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 714-725 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Principal peaks in the mass spectra of deoxynupharidine are accounted for on the basis of high resolution mass spectrometry and peak shifts in the mass spectra of deoxynupharidine-4-d1 and deoxynupharidine-6β, 7β-d2. Cleavage of the quinolizidine ring system of deoxynupharidine occurs predominantly in ring A, giving m/e 136, 107, 98, 94 and 81. The origins of the family of ions [M  -  alkyl]+ and m/e 178 are considered. A comparative survey is made of the occurrence of these ions, and others, in the mass spectra of piperidine, quinolizidine and thiospirane types of Nuphar alkaloids. Attention is directed toions useful in distinguishing structural types.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 169
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 744-752 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Mass spectra of ginsenoside-Rg1 deca-acetateSiehe Lit.2. and the related dammaran-type triterpene saponin acetates have been studied and a comment is given on the structure of panaxoside A (=ginsenoside-Rg1) proposed by Elyakov, et al .
    Notizen: Die Massenspektren von Ginsenoside-Rg1-decaacetat und verwandte Triterpensaponin-acetate vom Dammarantyp wurden untersucht. Die von Elyakov u.a. vorgeschlagene Struktur des Panaxoside A ( = Ginsenoside-Rg1)Siehe Lit. 3. wird kommentiert.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 170
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 763-773 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mass spectra and thermal decomposition of Rhodamine F5G hydrochloride have been studied in detail. Fragmentation schemes are presented which show that fragmentation in the mass spectrometer involves principally the substituents on the 9-phenylxanthhydrol nucleus. Mass spectral studies of the related compounds Rhodamine B500 hydrochloride, Rhodamine F5G hydroxide and Rhodamine F5G dihydrogen phosphate are also reported. The thermal decomposition of Rhodamine F5G hydrochloride leads to initial loss of ethyl chloride and formation of the zwitterion which rearranges at higher temperature to a lactone. The further pyrolysis has also been studied.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 171
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 774-780 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Elimination of CH3OH from the molecular ions of the methyl esters of cyclobut-3-ene-1, 2-dicarboxylic acids under electron-impact occurs to a much greater extent in stereoisomers having a trans configuration than in the cis analogues. Deuterium labelling shows that this process takes place via different mechanisms in the stereoisomeric esters. The abundance ratio [M — CH3OH]·+/[M — CH3O]+ is suggested as the most sensitive criterion for the deduction of configuration in this system. Determination of the geometry of the cyclobutene esters by n.m.r. spectroscopy as well as by pyrolysis to corresponding isomeric muconates is also discussed.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 172
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 826-830 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Electron-impact-induced oxygen transfer plays only a minor part in the fragmentation of N-(o-nitrobenzyl) amines. By investigation of 2H-labelled compounds, it could be established that the most important ions are formed by neighbouring group participation which leads to cyclisation of the fragment ions.
    Notizen: EIektronenstoßinduzierte Sauerstoffübertragungen spielen bei der Fragmentierung von N-(o-Nitrobenzyl)-Aminen nur eine untergeordnete Rolle. Durch die Untersuchung 2H-markierter Verbindungen wird belegt, daß die wichtigsten Ionen durch Nachbargruppenwechselwirkungen erzeugt werden, die zu einer Cyclisierung der Fragment-Ionen führen.
    Zusätzliches Material: 3 Tab.
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  • 173
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 837-839 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The fragmentation of four α-diazosulphones under conditions of electron-impact was studied with the aid of high resolution mass measurements and the metastable defocusing technique. An important difference from the spectra of the related α-diazoketones is the absence of peaks for [M — N2]+·. Metastables show, however, that these fragments probably exist as intermediates.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 174
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 51-59 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The rate constants for the replacement of water from the inner-coordination shell of Co(NH3)5OH23+, I, by dimethyl sulfoxide (DMSO) as DMSO gradually replaced water in the solvation shell of I were found to approach, and finally equal, the water-exchange rate constant of I in aqueous media in accordance with expectation for a dissociative mechanism. Also the rate constants for the replacement of DMSO from the innercoordination shell of Co(NH3)5DMSO3+, II, by water as water replaced DMSO in the solvation shell of II were found to approach, and approximately equal, the DMSO-exchange rate constant for II in liquid DMSO in accordance with expectation for a dissociative mechanism.The DMSO-exchange rate constant for II in liquid DMSO was determined and found to be equal to (3.6 ± 0.8) × 10-4 sec-1 at 45°C.The dissociation quotient, [II] [NO3-]/[Co(NH3)5NO32+], was found to be equal to 0.28 ± 0.11 M at 45°C by NMR methods. The pseudo first-order rate constants for anation of II by NO3- and the solvation of Co(NH3)5NO3 2+ by DMSO were determined at various temperatures.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 175
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 125-132 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The photochemistry of p-fluoranil in dioxane was studied by electron spin resonance (ESR) and the ESR-rotating sector technique. The transient photoradical is identified as the p-tetrafluorobenzosemiquinone neutral radical with a hyperfine splitting of 1.1 gauss for the hydroxy proton and the fluorine hyperfine splittings of 3.8 and 14.1 gauss for the meta and ortho fluorines, respectively. The radicals decayed by self-disproportionation with a second-order rate constant at room temperature of approximately 3.2 × 109M-1s-1. The activation energy of the decay process is found to be about 2.4 ± 0.4 kcal/mole.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 176
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 143-159 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The process of acetal hydrolysis is analyzed in terms of the competing steps of proton transfer and heavy atom reorganization. The results of this analysis are portrayed in a series of three-dimensional reaction coordinate diagrams. The observed pathway of hydrolysis (A-1, general acid catalyzed, or spontaneous) is shown to depend on the energy of the various possible intermediates in these reactions.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 177
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 161-167 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: First-order rate constants for formation of cyclohexanone and 2-cyclohexen-1-ol from 1,2-epoxycyclohexane and 1,2-epoxycyclohexane-3,3,6,6-d4 have been determined over the temperature range of 677-746°K. The observed kinetic isotope effects are used in an attempt to determine the mechanism for formation of products. A distinction between a biradical and a concerted mechanism for the alcohol formation could not be made. However, if a common biradical is the precursor of both cyclohexanone and 2-cyclohexenl-ol then the rate of ring closure of this biradical must be much faster than the rates of hydrogen transfer to give the ketone and the alcohol.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 178
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 229-244 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Translation-vibration (T-V) and vibration-vibration (V-V) energy transfer processes in the N2-CO2 system were investigated using classical trajectory techniques. Two empirical interaction potentials were employed. One is comprised of independent, atom-atom Morse-type functions operating between nonbonded atoms. The other included these atom-atom Morse functions plus Coulombic terms to account for the quadrupole-quadrupole intertion. Both interaction potentials led to similar T-V results. However, the result that CO2(v3) is excited ∼103 times more efficiently than N2(v = 1) was obtained, which is at variance with existing analytical theories of T-V energy transfer employing purely repulsive short-range potentials. Different V-V energy transfer probabilities were obtained from the two interaction potentials. The most important finding is that only when electrostatic orientation effects are combined with short-range repulsive interactions is the near-resonant \documentclass{article}\pagestyle{empty}\begin{document}$${\rm N}_{\rm 2} {\rm (}v = {\rm 1)} + {\rm CO}_{\rm 2} {\rm (000)} \to {\rm N}_{\rm 2} {\rm (}v = {\rm 0)} + {\rm CO}_{\rm 2} {\rm (001)}$$\end{document} V-V transfer found to be the dominant energy transfer path. This interaction potential also crudely accounts for the negative temperature dependence observed for this near-resonant V-V transfer at low temperatures (300-1000°K).
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 179
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 291-294 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Vibrationally excited pentyl-1, -2, and -3 radicals were formed selectively by the addition of thermal H atoms to the various pentene isomers with approximately 47 kcal/mole of vibrational energy. Decomposition products other than those expected, along with their pressure dependences, support the fact that either 1,2 or 1,3 hydrogen migrations with either a 3- or 4-member cyclic transition state is occurring with a ka of approximately 3 × 105 or 6 × 105 sec-1. A corresponding critical energy of 33 or 31 kcal/mole is found.
    Materialart: Digitale Medien
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  • 180
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Competitive studies of the reactions of ground-state oxygen atoms, generated by mercury-photosensitized decomposition of nitrous oxide, have been carried out with ethylene and all the fluoroethylenes using 2-(trifluoromethyl)-propene as reference compound. From measurements at 25°C and 150°C relative rate constants have been determined and used to calculate the Arrhenius parameters shown in the following table: TextOlefin\documentclass{article}\pagestyle{empty}\begin{document}$$\frac{{A_{{\rm olefin}} }}{{A_{{\rm 2TFMP}} }}$$\end{document}ΔERef\documentclass{article}\pagestyle{empty}\begin{document}$$\frac{{A_{{\rm olefin}} }}{{A_{{\rm C}_{\rm 2} {\rm H}_{\rm 4} } }}$$\end{document}ΔEC2H4CH2—CH21.10-1.18(1.0)(0)CH2—CHF1.030.840.942.02CH2—CF20.711.490.652.67CHF—CHF (cis-)1.231.921.123.10CHF—CHF (trans-)1.400.791.271.97CF2—CHF1.060.000.961.22CF2—CF20.86-3.220.78-2.04ΔERef = Eolefin - E2TFMP and ΔEC2H4 = Eolefin - EC2H4. Units are kJ/mole.The results are compared with corresponding data for other atoms and radicals, and discussed in terms of the electronic changes produced in the double bond by fluorine substitution, and in relation to the nature of the transition state.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 181
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 467-479 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Nucleophilic substitution reactions in the alkyl halides, RX + Y- → RY + X-, proceeding in polar media are considered on the basis of the theory presented in Part A. It is shown that the solvent reorganization energy is the main part of the activation energy for this processes. According to calculations performed, the values of the solvent reorganization energy equal ∼2.5-3 eV for H2O and ∼ 1.8-2.3 eV for acetone. From experimental data on the kinetic isotope effect, an estimate for the splitting of nonadiabatic terms and for the slope of the potential curve v′ of the intermolecular interaction between halide ion and methyl halide near transition configuration is made. Further, the parameter v′ is used for calculating the activation entropy of substitution reactions in the methyl halides. Theoretical activation energies and activation entropies agree with experimental values. In the framework of theory presented an interpretation of change of Ea and the preexponential factor with the type of alkyl halide is given.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 182
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 507-516 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Predictions of the “redox” and “complex” schemes for the Fe3+ catalyzed decomposition of H2O2 have been compared with published and new experimental data by numerical integratior of the appropriate complete sets of differential equations. Apparent discrepancies for the redox scheme at high Fe3+/H2O2 ratios are shown to disappear in the complete treatment, and inconsistencies of the complex scheme with both kinetic data and spectroscopic measurements are pointed out.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 183
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 517-526 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The photochemistry of 1,1,1-trifluoromethylazomethane has been partially characterized. The quantum yield for N2 formation from photolysis at 366 nm and room temperature was unity at low pressure and decreased to 0.5 at 630 torr. At room temperature the principal products were C2H6, C2F6, CH3CF3 (or CH2CF2 + HF at reduced pressures), plus substituted hydrazines, which mainly arise from addition of CF3 to the parent followed by combination of these radicals with CH3 or CF3. These fluorinated methyl hydrazine products detract from the general utility of CF3-N2-R compounds as sources for simultaneous study of the chemistry of CF3 and R radicals. At room temperature the hydrazine products accounted for more than 50% of the total yield; however, these products can be reduced by lowering the temperature and at 195°K their yields are negligible. The quantum yield for intramolecular (direct) formation of CH3CF3 + N2 was shown to be ≤0.002.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 184
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 545-552 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The addition of propene to cyclohexa-1,3-diene has been studied between 512 and 638°K at pressures between 70 and 640 torr. The products are endo- and exo-5-methylbicyclo [2.2.2] oct-2-ene, and their formations are second order. The rate constants (in 1./mole-sec) are given by \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k_{{\rm endo}} = - (26070 \pm 80)/4.576T + (5.74 \pm 0.03)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k_{{\rm exo}} = - (30090 \pm 80)/4.576T + (6.66 \pm 0.03)$$\end{document} The results are discussed in terms of a biradical mechanism.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 185
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 777-786 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Chloroethanes react with aqueous caustic to yield either elimination or substitution products. The reaction rates were measured for the dichloroethanes, trichloroethanes, tetrachloroethanes, and pentachloroethane between 283 and 353°K. The constants of HCl eleminations referring to the rate equation \documentclass{article}\pagestyle{empty}\begin{document}$$r = k[{\rm OH}^{\rm - }][{\rm dissolved \,substrate]}$$\end{document} are given by \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,2 - C}_{\rm 2} {\rm H}_{\rm 4} {\rm Cl}_{\rm 2} {\rm }\,k = 10^{10.99 \pm 0.03} \exp (- 23,000 \pm 50RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,1,2 - C}_{\rm 2} {\rm H}_{\rm 3} {\rm Cl}_{\rm 3} {\rm}\,k = 10^{13.99 \pm 0.03} \exp (- 22,400 \pm 50/RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,1,1,2 - C}_{\rm 2} {\rm H}_{\rm 2} {\rm Cl}_{\rm 4} {\rm }\,k = 10^{15.45 \pm 0.14} \exp (- 25,800 \pm 210/RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,1,2,2 - C}_{\rm 2} {\rm H}_{\rm 2} {\rm Cl}_{\rm 4} {\rm }\,k = 10^{16.40 \pm 0.05} \exp (- 22,550 \pm 70/RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm C}_{\rm 2} {\rm HCl}_{\rm 5} {\rm }\,k = 10^{12.50 \pm 0.08} \exp (- 15,200 \pm 110/RT)$$\end{document} all rate constants being in 1./mole·s and R in cal/mole· deg.With ethyl chloride, 1,1-dichloroethane, and 1,1,l-trichloroethane, the elimination is not observed and a slow substitution takes place. The influence of chlorine substituents on both sides of the molecule on mechanism and rate parameters is discussed.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 186
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The occurrence of anchimeric assistance in the vapor-phase thermolysis of anti- and syn-7-acetoxy-7-methylnorbornene and 7-acetoxy-7-methylnorborane has been investigated. The relative rates of thermolysis were found to be 1.9, 0.87, and 1.0, respectively. The nature of the transition state for ester thermolysis is discussed in light of the small amount of anchimeric assistance found in the thermolysis of the anti-isomer.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 187
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. 47-50 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: The results are presented of an intercomparison study between twelve investigators and three analytical techniques. The objective was to determine the precision and accuracy with which multi-element analysis of air particulates on filters can be accomplished using energy dispersive X-ray fluorescence spectrometry. Special emphasis was placed on testing calibration techniques and methods of correction for absorption in both particulate deposits and substrates. Results indicate that errors in calibration and correcting for substrate absorption can be reduced to much less than 10% for elements K and above, but the more work is required to test methods of correcting for particles size to achieve 10% accuracy at energies below 3 keV.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 188
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: This work is aimed at providing a direct analytical method for powdered materials collected on cellulose filters. The origin and composition of these materials may be very different. The analytical technique employed was X-ray fluorescence spectrometry without preliminary treatment of samples.It is known that different thickness of thin deposits, due for example to different sampling condition, cause some difficulties on the correct accomplishment of the analysis. To eliminate this drawback the basic principles characterising the behaviour of X-ray penetration in the matter, were developed, thus leading to some equations, applicable to the analysis of the following kinds of samples: (a) sample of infinite thickness for X-ray penetration; (b) sample of finite thickness below the critical value; (c) sample of infinite thickness placed over the sample of finite thickness.The equation relating to case (c) was then applied to the analysis of powdered materials collected on cellulose filters.A suitable plate of a selected metal was placed over the sample, and the fluorescence radiations intensity values of the element to be analysed were recorded together with the intensity of the radiation emitted by the plate.By substituting some terms of the above mentioned equation with experimental data, X-ray intensity values were corrected, and then independent measurements were performed on the sample thickness.This work described both the theoretical part and the experimental procedures with results showing the method's reliability.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 189
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. A13 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 190
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 191
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. A14 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 192
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. A14 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 193
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. A15 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 194
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974) 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 195
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. 101-101 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 196
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. 102-108 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: Fluorescence crossed effects are discussed as to their exact significance, and relative importance regarding quantitative analysis. While they do not occur in binary systems, crossed effects appear when a fluorescent element is influenced by two or more interfering elements, more particularly when it is subject to enhancement effects. Dissociating crossed effects from pure binary interactions enabled us to establish an accurate general equation for expressing interelement effects in accordance with fundamental theory, and then the associated corrections in any analytical system. As a rule, practical applications should include some suitable modification of the general formula, with respect to the magnitude of corrections for the particularsystem considered.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 197
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. A21 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 198
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. 151-152 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: In X-ray fluorescence, as well as other quantitative methods for determining trace metal concentrations, computer methods for extracting characteristic peaks from background are very important. Cases where background is large and nonlinear, or there are overlapping peaks, present difficulties in the development of simple computer programs which give an accurate analysis of the peak. The method of analysis that will be described here was developed to meet these demands. The basic concept is simple, and good accuracy and reproducibility are achieved in samples with large nonlinear background, as well as overlapping peaks. The analysis is essentially independent of background.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 199
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. 153-158 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: The pulsed beam technique has been used to achieved a high data acuumulation rate in an energy-dispersive analytical system consisting of an electron probe analyser and the Harwell ‘Highspec’ pulse analyser system 3074. The use of fast beam switching ( ∼ 30 ns transient time) and the special timing facilities available in the Harwell equipment reduce the spectrum contamination due to displacement of the probe during switching to a low level and also provide precise measurements of live time, essential for accurate analysis. Analyses performed at spectrum accumulation rate of up to 12 kP.P.S. shows agreement with accepted values to within ± 1% for major constituents. Simple modification of the system permits accumulation rates up to 25 kP.P.S.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 200
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 3 (1974), S. 167-169 
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: A mathematical approach for determining Ba/Ti molar ratios of barium titanates has been made. A computer program applies the necessary corrections for absorption and secondary fluorescene. The method requires no standards and appears to be sufficiently accurate over large compositional variations. Evaluations of the magnitude of the secondary fluorescence contributions on TiKα intensities are given.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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