Perylene-3,4-dicarboxylic imides are prepared by a new decarboxylizing condensation with moderately sterically hindered primary amines. Perylene-3,4-dicarboxylic anhydride is prepared via a saponification reaction of the dicarboximide and is a starting material for a number of new types of chromophores. A second route to novel perylene derivatives is a partial hydrolysis of perylene dyes and a condensation with diamines. The dyes thus obtained are orange to red fluorescing in solution.
CITATION STYLE
Langhals, H. (1994). Novel Perylene Derivatives as Highly Photostable Fluorescent Dyes. CHIMIA, 48(11), 503. https://doi.org/10.2533/chimia.1994.503
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