Novel Perylene Derivatives as Highly Photostable Fluorescent Dyes

  • Langhals H
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Abstract

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.

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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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