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  • 1970-1974  (9)
  • Analytical Chemistry and Spectroscopy  (6)
  • Physics  (3)
  • Organic Chemistry
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1169-1175 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly-4,4′-oxydiphenylenesulfonyl and poly-4,4′-methylenediphenylenesulfonyl were synthesized by an electrophilic substitution polymerization of the arylene monosulfonyl chloride monomers. The glass-transition temperatures Tg of these polymers were determined by calorimetric and dynamic mechanical measurements, and the number-average molecular weights were determined by vapor-pressure osmometry. Both polymers were found to have the same Tg at equivalent molecular weight; the limiting value at high molecular weight is 238°C. Both polymers have two dynamic mechanical relaxation peaks at temperatures far below Tg. One is in the neighborhood of 0°C, and the other is at -110°C. Plausible origins for these relaxations, and the absence of any near 0°C in poly(4,4′-isopropylidenediphenylene-co-4,4′-sulfonyldiphenylene dioxide), are discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 275-287 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As model polymers for isolated short-chain branches in low-density polyethylene, a series of ethylene-1-olefin copolymers was examined by use of 13C NMR at 25.2 MHz. An array of 13C resonances was observed that could be associated independently with methyl through amyl branches. The 13C chemical shifts became insensitive to branch length with hexyl and longer branches. Assignments of the various carbon resonances associated with branching were accomplished by using off-resonance decoupling techniques and the behavior of alkane chemical shifts previously observed by other investigators. The ratio of certain backbone and branch resonances could be used to establish the short-chain branch distribution in a low-density polyethylene.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 737-758 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric dispersions of reconstituted collagens and gelatin were measured from 0.1 to 10 kHz and -160 to +160°C. At 0.1 kHz there is a γ transition at -80°C which is attributed to the H2O-coupled local modes. The process has an activation energy of 7.5 kcal. A devitrification process is observed at 10-20°C. Both of these processes have their counterparts in the dynamic mechanical measurements. The tan δ values are up to 3 times as great for the dynamic mechanical dispersions. There is an additional hightemperature dielectric loss transition which does not correspond to any seen with the mechanical experiments. A probable mechanism for this absorption is the Maxwell-Wagner-Sillars effect.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 1055-1066 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron-impact mass spectra and the field ionization mass spectra of 1-chloro-2-nitrosocyclohexane and 1-chloro-2-nitrosocyclopetane are presented and discussed. The two compounds investigated exist in dimeric form in the gaseous phase.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1970), S. 503-512 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Five phenarsazine derivatives with arsenic in the trivalent state and the pentavalent state are studied by mass spectrometry. Their characteristic fragmentation modes and the fragment ions with common structures are discussed. Experimental results show that the pyrolytic decompositions of the phenarsazine derivatives are closely parallel to the unimolecular ion fragmentation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 287-302 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nine phenoxarsine derivatives with arsenic in the trivalent state and the pentavalent state are synthesized and studied by mass spectrometry. Their characteristic fragmentation modes and the fragment ions with common structures are discussed. Phenoxarsinic acids are found to be unstable in the gaseous phase at the temperatures studied and tend to form their corresponding anhydrides.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 833-841 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The EI Mass spectra of the polyfunctional pentaerythritol derivatives show that the molecular ions [M]+· exhibit extensive ion fragmentation. No Information about [M]+·. can be obtained. In Contrast to this, the FI Mass spectra of these compounds show intense [M]+· and/or [M + 1]+, and a characteristic ion at m/e 31, which is assumed to be the oxonium ion \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_2 = \mathop {\rm O}\limits^ + {\rm H} $\end{document}. Because of surface adsorption and field attraction, FI mass spectrometry presents a serious problem in quantitative analysis of a mixture containing compounds with quite different degrees of polarization.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 747-751 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The predicted pyrolyzate of phenoxarsine derivatives from their mass spectra is diphenylene oxide. The prediction is verified by the experiment.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 493-500 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermally and electron-impact-induced rearrangements of the dimethylthioncarbamates to the dimethylthiolcarbamates are discussed. Owing to the competition with the ion fragmentation reactions in the mass spectrometric time, 〈 10-6 seconds, the extent of the mass spectrometrically observed ion isomerization cannot be predicted from that of the thermal induced one. In the ion fragmentations of the non-rearranged molecular ions, it was found that the relative abundance of the ion (CH3)2NC≡O⊕ to the total ionization is larger than that of the ion (CH3)2NC≡S⊕. This is believed to be attributable to the differences in the dissociation energies of the C—S bond and the C—O bond and in the stabilities of the two ions.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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