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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 453-460 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The concept that the slow, unimolecular reactions of the homologous series of radical cations are largely determined by the relative energetics of the possible product combinations is discussed. The concept is shown to provide a reasonably consistent rationalization of the known metastable dissociations of and correctly predicts the reactions undergone by . The concept may be useful in discussing the unimolecular chemistry of isomers.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 475-476 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method for estimating the heats of formation of gaseous, open chain cations via a suitable isodesmic substitution is reported.
    Additional Material: 2 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1978), S. 721-728 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unimolecular decompositions of two isomers of [C3H8N]+, \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH} = \mathop {\rm N}\limits^ + {\rm H}_2 $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm N}\limits^ + {\rm H = CH}_{\rm 2} $\end{document}, are discussed in terms of the potential energy profile over which reaction may be considered to occur. The energy needed to promote slow (metastable) dissociations of either ion is found to be less than that required to cause isomerization to the other structure. This finding is supported by the observation of different decomposition pathways, different metastable peak shapes for C2H4 loss, the results of 2H labelling studies, and energy measurements on the two ions. The corresponding potential energy profile for decomposition of the oxygen analogues, \documentclass{article}\pagestyle{empty}\begin{document}${\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH =\!= }\mathop {\rm O}\limits^ + {\rm H} $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm O}\limits^ + {\rm = CH}_{\rm 2} $\end{document}, is compared and contrasted with that proposed for the [C3H8N]+ isomers. This analysis indicates that for the oxygen analogues, the energy needed to decompose either ion is very similar to that required to cause isomerization to the other structure. Consequently, dissociation of either ion is finely balanced with rearrangement to the other and similar reactions are observed. Detailed mechanisms are proposed for loss of H2O and C2H4 from each ion and it is shown that these mechanisms are consistent with 2H and 13C labelling studies, the kinetic energy release associated with each decomposition channel, the relative competition between H2O and C2H4 loss and energy measurements.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1976), S. 223-230 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that the ‘metastable’ mass spectra of a series of monosubstituted benzenes are consistent with reaction over the lowest available energy surfaces. The non-occurrence of some qualitatively possible decomposition pathways may therefore be used to place lower limits on the heats of formation of gaseous cations. Conversely, where characterized reactions are preempted by new reactions upon introduction of additional substituents, upper limits may be placed upon the heats of formation of the ionic products of the new reactions. The concepts are employed to deduce that C3H6 elimination from n-butylbenzence subsequent to ionization leads to ionized toluene rather than ionized methyleneclohexadience.
    Additional Material: 3 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1978), S. 330-337 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The slow unimolecular dissociations of six members of the [CnH2n-3]+ (n = 3-8) series of unsaturated carbonium ions are explained in terms of a potential surface approach together with some concepts of mechanistic organic chemistry. The occurrence of some dissociations is shown to be precluded because either the reacting configurations or product combinations are inaccessible at energies appropriate to metastable transitions. The approach permits correct predictions to be made concerning the shapes of metastable peaks for dissociations which occur without σ-bond formation in the final step. In particular, the observation of a composite peak, thus indicating two channels for reaction, for C2H4 loss from [C7H11]+ is naturally accommodated.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 254-260 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The extent of C-methylation, an artifact of the permethylation procedure used to derivatize peptides for mass spectrometric sequencing, was investigated by mass spectrometry. Ten glycine-containing peptides were N-acetylated and then permethylated by the Hakomori method and analyzed by chemical ionization and, in some cases, by electron ionization mass spectrometry. A comparative study was made of the tripeptides Gly Pro Ala and Ala Pro Gly, derivatized by three permethylation procedures. The results show that while C-methylation occurs primarily at glycine, other amino acids (Gln, Glu, Met, Tyr) are also C-methylated, but to a lesser degree. The extent to which C-methylation occurs varies widely and depends on residue position and on the identity of neighboring residues. Such artifacts could lead to serious errors in peptide sequences determined by mass spectrometry, especially when mixtures of peptides are analyzed.
    Additional Material: 4 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 164-167 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical ionization mass spectra of eleven biomedically significant quaternary amimes are reported. The samples are converted to volatile compounds by known thermal decompositions. Chemical ionization of the compounds gives simple, easily identifiable spectra which are useful for the analysis of the original samples.
    Additional Material: 4 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1977), S. 159-171 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical ionization mass spectrometry is used at low resolution to determine the sequences of permethylated acetyl peptides. The method has been tested with 45 peptides, between 2 and 5 residues long, including examples of all of the common amino acids except cysteine and N-terminal asparagine. The isobutane chemical ionization spectra contain three principal types of N-terminal sequence ion and one type of C-terminal sequence ion. The redundant information available from these four types of sequence ion increases the reliability of the sequence determination. In prospect, isobutane chemical ionization mass spectrometry seems to be a useful technique for peptide sequence determination, and may have advantages in some cases.
    Additional Material: 2 Ill.
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  • 9
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The concept of surface-active comonomers of higher functionality is propsed as a means of increasing reliability of the bonding between preventive and restorative dental materials and tooth structures.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 12 (1978), S. 505-515 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Initial rates of ion-exchange adsorption of nickelous or cupric ions with calcium ions on the surface of synthetic hydroxyapatite were studied in aqueous nitrate solutions. A kinetic interpretation has been proposed. The determination of the initial rates is important for a systematic investigation of adhesion of certain properly designe substances that may mediate a chemical bonding between dental resins and “moralanted” calcified tissues.
    Additional Material: 4 Ill.
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