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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 893-897 
    ISSN: 0009-2940
    Keywords: 4,4′-Distyrylazobenzenes, alkoxy- ; Siegrist Reaction ; Liquid crystals ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4,4′-Distyrylazobenzene as MesogenFrom 3,4-dihydroxybenzaldehyde (1) the tetraalkoxy-substituted 4,4′-distyrylazobenzenes (E,E,E)-5a - c are synthesized. A similar reaction sequence leads from ethyl 3,4,5-trihydroxy-benzoate (6) to the hexaalkoxy-substituted 4,4′-distyrylazobenzenes (E,E,E)-11 b, c. With the exception of 5a all products show thermotropic LC properties. Smectic phases have been characterized by polarizing microscopy and by differential scanning calorimetry.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 889-892 
    ISSN: 0009-2940
    Keywords: Wittig reaction ; Siegrist reaction ; Azo compounds ; Photochemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4,4′-Distyrylazobenzene as Chromophore4,4′-Distyrylazobenzenes are prepared from 4,4′-dimethylazobenzene. Whereas the Siegrist method furnishes stereoselectively the (E,E,E) configuration, a Wittig olefination leads to a mixture of (Z,E,Z), (Z,E,E) and (E,E,E) isomers which can be easily separated. Irradiation of the intense absorption at λ ≈ 400 nm causes a selective (E) → (Z) isomerization of the N = N bond of all three isomers. The reverse reaction takes part in the photochemical equilibration, moreover, it is a thermal process with a relatively low activation barrier.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 121 (1988), S. 1609-1615 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Photochemistry of Electron-Rich 1,3-DistyrylbenzenesThe 1,3-distyrylbenzenes 3, containing up to seven alkoxy groups, are subjected to the oxidative photocyclization. Elimination of methanol (3bb → 7bb, 3bf → 7bf) and quinone oxidation can occur as competitive or consecutive reactons in the formation of the products 6,7 and 8. Selfsensitized generation of singlet oxygen by 6bf can lead to endoperoxide formation (6bf → 11).
    Notes: Die 1,3-Distyrylbenzole 3 mit bis zu sieben Alkoxygruppen werden der oxidativen Photocyclisierung unterworfen. Bei der Bildung der Produkte 6, 7 und 8 können als Konkurrenz- bzw. Folgeprozesse die Abspaltung von Methanol (3bb → 7bb, 3bf → 7bf) und die Chinonoxidation (3cf → 8) auftreten. Die eigensensiblisierte Erzeugung von Singulettsauerstoff kann bei 6bf zur Endoperoxidbildung führen (6bf → 11).
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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