Band 6, Heft 8

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.

Colorants based on the anthraquinone structure are categorized as a subclass of carbonyl colorants. Anthraquinone textile dyes rank second in importance to azo dyes, especially within the vat dye application class. Vat dyes became of interest to the pigment industry because of their insolubility. This insolubility and generally excellent fastness properties inspired investigations into the selection of suitable established anthraquinonoid vat dyes for use as pigments after conversion to a physical form that is appropriate for their applications. Originally this proved difficult, but was eventually achieved following the development of appropriate conditioning after treatment processes. The structural chemistry of the various types of anthraquinonoid pigments in relation to their technical and coloristic performance is discussed. The chapter concludes with an illustrated description of the main synthetic routes and finally with a description of the principal applications of the individual commercial products. Anthraquinonoid pigments are generally regarded as high-performance products, suitable for highly demanding applications, although they tend to be expensive.

This article covers three closely related types of colorant: the indophenol class of dyes plus those of their indaniline and indamine counterparts. Their roots stretch all the way back to the mid-nineteenth-century period during which synthetic dyes were successfully commercialized for the first time. The early history and subsequent development of these classes are briefly surveyed along with their chemistry. Two of their most important applications involve the synthesis of the dyes as part of the coloration process: the development of images from photographic film and the dyeing of hair. This introduction to indo dyes closes by describing their role in these and other coloration processes.

The monoazoacetoacetanilide series of pigments, traditionally known as Hansa Yellows, are long-established products that entered the market in the early twentieth century. They are mostly inexpensive products offering bright colors of moderate intensity covering the entire yellow area of the spectrum, good lightfastness, but inferior solvent resistance. The technical properties of the pigments may be explained by their molecular structures, which adopt the ketohydrazone tautomeric form, and their crystal structures. Their good lightfastness is attributed mainly to intramolecular hydrogen-bonding, while their generally inferior fastness to organic solvents is explained by the relatively weak intermolecular interactions in the crystal structure. The monoazoacetanilide pigments are synthesized by the traditional two-stage process of diazotization of a primary aromatic amine, followed by an azo coupling reaction of the resulting diazonium salt with an acetoacetanilide coupling component. Their main use is in decorative paints, although a few products are suitable for printing inks.

This article furnishes an introduction to one of the most well-known classes of photochromic colorant. While the properties of spiropyran dyes inspired pioneering efforts to exploit photochromism for industrial applications, their lack of robustness held them back from commercialization. Nevertheless, this type of dye remains at the heart of much of the work to develop light-responsive materials upon which many potential applications in different fields of scientific and technological endeavor depend. The article describes the photochromism, synthesis, and applications of spiropyran colorants with an emphasis on the structural subtype that has attracted the greatest scrutiny. It also acts as a springboard to sources of more detail on these aspects.

Zinc sulfide pigments belong besides titanium dioxide and zinc oxide pigments to the most important inorganic whites. The pigments are mostly used in primers, plastics, fillers, putties, artists’ colors, and emulsion paints. Zinc sulfide pigments are divided into pure zinc sulfide (ZnS) and lithopone (mixtures of ZnS with BaSO 4 ) pigments. They are synthesized using precipitation processes in aqueous medium. Compared with pure zinc sulfide pigments, lithopone pigments have a much larger technical importance.