Jump to content

Triarylmethane dye

From Wikipedia, the free encyclopedia

Triarylmethane dyes are synthetic organic compounds containing triphenylmethane backbones. As dyes, these compounds are intensely colored. They are produced industrially as dyes.[1]

Families

[edit]

Triarylmethane dyes can be grouped into families according to the nature of the substituents on the aryl groups. In some cases, the anions associated with the cationic dyes (say crystal violet) vary even though the name of the dye does not. Often it is shown as chloride.

Methyl violet dyes

[edit]

Methyl violet dyes have dimethylamino groups at the p-positions of two aryl groups.

Fuchsine dyes

[edit]

Fuchsine dyes have primary or secondary amines (NH2 or NHMe) functional groups at the p-positions of each aryl group.

Phenol dyes

[edit]

Phenol dyes have hydroxyl groups at the p positions of at least two aryl groups.

Malachite green dyes

[edit]

Malachite green dyes are related to the methyl violet dyes, except that they contain one phenyl (C6H5) group.

Victoria blue dyes

[edit]

Victoria blue dyes are related to the methyl violet dyes, except they contain one naphthylamino group. Variation is found is dimethylamine vs diethylamino substituents on the phenyl rings and variations of the secondary amine on the naphthyl group.

Xanthene dyes

[edit]

Xanthene dyes feature a xanthene core. They are not widely used as textiles, but for other applications.

Bridged arenes

[edit]

Where two of the aryl groups are bridged by a heteroatom, these triarylmethane compounds may be further categorized into acridines (nitrogen-bridged), xanthenes (oxygen-bridged), and thioxanthenes (sulfur-bridged).

Synthesis

[edit]

The amine-containing dyes are often prepared from Michler's ketone or its diethylamino analogue. In this way, the third aryl group is readily differentiated. The Friedel–Crafts alkylation reaction is a popular method to prepare many of the phenolic derivatives:

Friedel–Crafts synthesis of thymolphthalein

Applications

[edit]

In addition to their dominant use as dyes, many of these dyes react reversibly with acid and base, and thus serve as pH indicators.[1]

Bromocresol green reacts with acids and bases to give differently colored compounds


See also

[edit]

References

[edit]
  1. ^ a b Gessner, Thomas; Mayer, Udo (2000). "Triarylmethane and Diarylmethane Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a27_179. ISBN 978-3527306732.