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  • Articles: DFG German National Licenses  (4)
  • Organic Chemistry  (3)
  • molecular semiconductors  (1)
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  • Articles: DFG German National Licenses  (4)
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  • 1
    ISSN: 1572-8951
    Keywords: Organic-based devices ; molecular semiconductors ; field-effect transistors ; charge transfer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Conjugated polymers, e.g., polyacetylene and polythiophenes, conjugated thiophene oligomers and metallophthalocyanines have been proposed in the literature as organic semiconductors for the fabrication of organic-based field-effect transistors, FET. The poor performances generally shown by these FET have been attributed to the very low carrier mobility in organic semiconductors, and the improvement of this parameter has been the objective of a large number of works. The analysis of the mode of operation of organic-based FET, which operate through the formation of an accumulation layer, shows that an ohmic contribution has to be taken into account in the total observed current output of the devices. The conductivity of the organic semiconductor plays thus a significant role in the FET characteristics, although this point has been up to now rarely considered. In this regard, most of the claims in the literature about high mobility achievements are shown to be of limited significance. Conjugated oligomers are actually the only class of organic semiconductors presenting high mobility together with low conductivity, which, furthermore, indicates that interchain transfer of charge may be a much more efficient process than generally believed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 58 (1975), S. 2563-2574 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nous avons synthétisé une série de spiropyrannes benzoxathioliques par un processus en deux étapes: obtention de perchlorates styryliques en milieu acide par condensation simultanée de trois substrats intermédiaires, puis cyclisation en milieu basique. Un mécanisme est proposé.Ces spiropyrannes benzoxathioliques sont photochromes et nous avons étudié la cinétique de décoloration thermique ainsi que l'absorption visible de leurs photomérocyanines. Des observations comparables à celles enregistrées en série benzodithiolique nous ont amenés ici encore à envisager une structure de type quinonique pour la mérocyanine.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nous avons étudié la transformation réversible de spiropyrannes benzodithioliques photochromes en mérocyanines: les spectres d'absorption de celles-ci et leurs cinétiques de décoloration thermique sont suivis en utilisant un spectrophotomètre à enregistrement rapide couplé à un appareil de photolyse-éclair. Les nombreuses inversions constatées par rapport aux résultats cinétiques obtenus en série benzothiazolinique pour des composés identiquement substitués, associées à des considérations sur les spectres visibles des photomérocyanines et à des effets de polarité de solvant, nous amènent à envisager pour les mérocyanines benzodithioliques une structure de type quinonique alors qu'en série benzothiazolinique une structure de type dipolaire a été mise en évidence.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of spiropyrans 11 and 12 and spirooxazines 13-17 containing a thiophene moiety is described. Two different synthetic approaches were used. The spectrokinetic properties of these new compounds are reported.
    Type of Medium: Electronic Resource
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