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  • Articles: DFG German National Licenses  (4)
  • Electronic Resource  (4)
  • Dyes, fluorescent  (3)
  • Carboximides  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Synthese von 1,7-Diazaperylen (1990)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 1881-1884 
    Details
    ISSN: 0009-2940
    Keywords: 1,7-Diazaperylene ; Dyes, fluorescent ; Fluorescence, slid-state ; Meerwein arylation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of 1.7-DiazaperyleneThe hitherto unknown 1,7-Diazaperylene (2) has been prepared in a five-step synthesis from 1,5-diaminoanthraquinone (3) by a Meerwein arylation reaction. Applications as a fluorescent dye are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19901230920
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Synthese von Reinst-Rubicen und Rubicen-Derivaten (1990)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 1981-1987 
    Details
    ISSN: 0009-2940
    Keywords: Rubicene ; Hydrocarbons, polycyclic ; Dyes, fluorescent ; Singlet oxygen sensitizer ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Highly Pure Rubicene and Rubicene DerivativesA simple one-step synthesis of highly pure rubicene (2) from fluorenone (1) and magnesium with 24% yield is described and compared with other preparation procedures. Mono- and disubstituted rubicene derivatives are prepared by electrophilic aromatic substitution.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19901231009
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Synthesis of perylene-3,4-dicarboximides  -  Novel highly photostable fluorescent dyesDedicated to Prof. Dr. Christoph Rüchardt on the occasion of his 65th birthday. (1995)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1995 (1995), S. 1229-1244 
    Details
    ISSN: 0947-3440
    Keywords: Fluorescent dyes ; Pigments ; Perylenes ; Carboximides ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Perylene-3,4-dicarboximides 2 are obtained by a decarboxylizing condensation of moderately sterically hindered primary amines with perylene-3,4,9,10-tetracarboxylic 3,4:9,10-bisanhydride (3) in the presence of water. Perylene-3,4-dicarboxylic anhydride (4) is prepared by hydrolysis of the imides with KOH in tert-butyl alcohol. The anhydride may be condensed with any primary amine to the corresponding imide. The imides are highly fluorescent and very photostable dyes.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.1995199507164
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Perylenamidine-imide dyes (1995)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1995 (1995), S. 481-486 
    Details
    ISSN: 0947-3440
    Keywords: Dyes, fluorescent ; Perylene derivatives ; Heterocyclic rings ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Perylene-3,4:9,10-tetracarboxylic acid 3,4-anhydride-9,10-imides are condensed with primary diamines to a number of new basic chromophores with amidine-imide structures. Lightfast dyes are obtained which exhibit a strong fluorescence in solution. The absorption and fluorescence spectra of the title compounds are bathochromically shifted compared to those of the perylene dyes.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.199519950366
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    Paper (German National Licenses)
    Fulltext
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