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## Abstract 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.

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Author

Leonhard Feiler; Heinz Langhals; Kurt Polborn

Publisher

John Wiley and Sons; Wiley (John Wiley & Sons); VCH Verlagsgesellschaft; Wiley (ISSN 0947-3440)

Published

1995

Language

EN

Field

Chemistry (Physical Sciences)