Abstract
Since their industrial introduction in the 1980s, DPP pigments now constitute a highly important group of high-performance carbonyl pigments. The DPP system was first discovered by accident in 1974, and was subsequently re-investigated by Ciba Geigy who recognized its potential to provide commercial organic pigments. DPP pigments exhibit strong similarities compared with quinacridone pigments, in terms of their molecular and crystal structures and their properties, including low solubility and excellent fastness properties. X-ray crystal structural analysis has demonstrated that their technical performance is the result of intermolecular hydrogen bonding and π–π stacking interactions in the crystal lattice structure. Based on a simple retrosynthetic analysis, an efficient synthetic process was developed by Ciba Geigy for their large-scale manufacture. DPP pigments currently provide orange through to reddish violet shades and have become of special importance in providing brilliant saturated red shades with the outstanding durability required for applications such as automotive paints.
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Articles in the same Issue
- Frontmatter
- Editorial: Advanced chemoinformatics applications at the service of natural product discovery
- Combinatorial library design and virtual screening of cryptolepine derivatives against topoisomerase IIA by molecular docking and DFT studies
- Chemical similarity methods for analyzing secondary metabolite structures
- Carbonyl pigments: miscellaneous types
- Diketopyrrolopyrrole (DPP) pigments
Articles in the same Issue
- Frontmatter
- Editorial: Advanced chemoinformatics applications at the service of natural product discovery
- Combinatorial library design and virtual screening of cryptolepine derivatives against topoisomerase IIA by molecular docking and DFT studies
- Chemical similarity methods for analyzing secondary metabolite structures
- Carbonyl pigments: miscellaneous types
- Diketopyrrolopyrrole (DPP) pigments