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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1983), S. 462-465 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogenation reactions, both brominations and chlorinations, of haloorganics lead to di- or often polyhalogenated products. A major mechanistic question concerning these reactions always remains unanswered; whether they proceed by direct substitution or whether they proceed by a process involving an elimination-readdition sequence. The question can be answered by carrying out the reactions using isotopically enriched halogen. A method of analysis has been devised, using high resolution mass spectrometry, which determines the isotopic distribution in each of the individual halogen atoms. The details of this procedure are presented in this report and examples of its use from several mechanistic investigations are presented.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 6 (1996), S. 353-357 
    ISSN: 1057-9257
    Keywords: IR ; TEA(TCNQ)2 ; phase transition ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: Polarised infrared and optical spectra were measured at temperatures between 5 and 300 K to study the 210 K structural phase transition in the organic charge transfer salt TEA(TCNQ)2. At high temperatures, characteristic spectral features of semiconducting 1:2 TCNQ salts are observed. At low temperatures, several changes are found. First, the electronic charge transfer sharpens and has enhanced oscillator strength in the low-temperature phase. Second, the vibrational lines split into clear doublets, whose appearance is associated with a sharp decrease in the phonon damping at low temperatures.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2395-2404 
    ISSN: 0887-6266
    Keywords: polyphenylenes ; luminescence ; broken conjugation ; discrete emitter center ; charge defect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Optical absorption and photo-luminescence measurements were performed on a series of semiconducting polymers, based upon phenylene linkages, that have discrete emitter units. In these polymers, broken conjugation has been achieved in two ways: by introducing metalinkages between various numbers of para-connected aromatic groups or by severe steric distortion of a fully conjugated main chain. In either case, electronic states are localized on relatively small units, resulting in a large (π, π*) band gap. The band gap decreases with increasing emitter unit conjugation, as expected. Blue light emission was observed from these materials, with the peak emission wavelength red shifted (by greater than 1 eV on average) from the peak absorption. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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