Startseite Carbonyl pigments: General principles
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Carbonyl pigments: General principles

  • Robert Christie EMAIL logo und Adrian Abel
Veröffentlicht/Copyright: 29. Juni 2021
Veröffentlichen auch Sie bei De Gruyter Brill

Abstract

This chapter describes the general features of the chemical class of pigments designated as carbonyl pigments. These pigments are characterized by the presence of carbonyl groups linked to one another via an extended conjugated system, often forming polycyclic aromatic structures. Carbonyl pigments have experienced distinct phases in their histories. Certain carbonyl colorants, notably anthraquinonoids, were discovered in the early twentieth century and subsequently used as vat dyes for textiles, but their potential as high-performance pigments was not realized until the mid-twentieth century when demand began to emerge for pigments of the quality that they could provide. After conversion to a suitable physical form, several vat dyes were then introduced as vat pigments. Several other carbonyl pigment types did not originate as vat dyes but were developed specifically for pigment use. Carbonyl pigments provide a wider diversity of structural arrangements. The broad carbonyl chemical class may be categorized into several sub-types, each with its own characteristic structural features. These categories, which are discussed in separate chapters, include anthraquinonoids, quinacridones, diketopyrrolopyrroles, perylenes, perinones, indigoids, isoindolines, isoindolinones, and quinophthalones. These products generally owe their high levels of technical performance to their large molecular size and high molecular planarity, which lead to highly compact crystal structures and, in many cases, to the ability of the carbonyl group to participate in strong intra- and intermolecular hydrogen bonding.

References

1. Hallas G. In colorants and auxiliaries: organic chemistry and application properties. In: Shore J,editor. Bradford: society of dyers and colourists. vol. 1, ch.6 1990.Suche in Google Scholar

2. Zollinger H. Color chemistry: syntheses, properties and applications of organic dyes and pigments, 3rd ed. Weinheim: Wiley-VCH, Ch. 8 2003.Suche in Google Scholar

3. Gordon PF, Gregory P. Organic chemistry in colour. New York: Springer-Verlag, Ch. 4 1983.10.1515/9783112541746Suche in Google Scholar

4. Christie RM. Colour chemistry, 2nd ed. London: RSC, Ch 4 2015.10.1039/9781782626510Suche in Google Scholar

5. Hunger K, Schmidt MU. Industrial organic pigments. 4th ed ed. Weinheim: Wiley-VCH Verlag GmbH, 2019.Suche in Google Scholar

6. Chenciner R. Madder red: a history of luxury and trade, plant dyes and pigments. Richmond: Curzon, 2000.Suche in Google Scholar

7. Balfour-Paul J. Indigo. London: British Museum Press, 1998.Suche in Google Scholar

8. Sharvin VV. J Rus Phys Chem Soc. 1915;47:1260.Suche in Google Scholar

9. Liebermann H. Über die Bildung von Chinakridonen aus p-Di-arylamino-terephtalsäuren. 6. Mitteilung über Umwandlungsprodukte des Succinylobernsteinsäureesters. Annalen Der Chemie. 1935;518:245.10.1002/jlac.19355180115Suche in Google Scholar

Published Online: 2021-06-29

© 2020 Walter de Gruyter GmbH, Berlin/Boston

Heruntergeladen am 10.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/psr-2020-0153/pdf?lang=de
Button zum nach oben scrollen