Diketopyrrolopyrrole cocrystals
View Patent ↗The invention relates to cocrystals of compounds of the formulae (I), (II) and (III), obtainable by reacting 1 mol of a succinic diester with 2 mol of a mixture of nitriles A-CN and B—CN, where A-CN and B—CN are present in the nitrile mixture in a molar ratio of 90:10 to 30:70 relative to one another, and where A-CN is 2-chlorobenzonitrile and B—CN is 4-X-benzonitrile where X=chlorine, methyl or nitrile.
1. A mixed crystal comprising compounds of formula (I), (II) and (III),
obtained by reacting 1 mol of a succinic diester with 2 mol of a mixture of nitriles A-CN and B—CN, in a molar ratio of 90:10 to 30:70 between the A-CN and B—CN in the mixture of nitriles, A-CN being 2-chlorobenzonitrile and B—CN being 4-X-benzonitrile where X=chlorine, methyl or nitrile.
2. The mixed crystal as claimed in claim 1 , obtained by reacting 1 mol of a succinic diester with 2 mol of the mixture of nitriles A-CN and B—CN in a molar ratio of 80:20 to 40:60 between the A-CN and B—CN in the mixture of nitriles.
3. The mixed crystal as claimed in claim 1 obtained by reacting 1 mol of a succinic diester with 2 mol of a mixture of nitriles A-CN and B—CN in a molar ratio of 75:25 to 50:50 between the A-CN and B—CN in the mixture of nitrites.
4. The mixed crystal as claimed in claim 1 , wherein X is chlorine.
5. The mixed crystal as claimed in claim 1 , wherein the main signals in the x-ray powder diagram
2 theta:
relative intensity:
5.9
S
13.4
M
15.8
M
25.5
M
26.5
M
wherein the x-ray powder diagram is Cu—K α radiation, 2 theta values in degrees, measuring accuracy +/−0.2° intensities: s=strong, m=medium.
6. A process for preparing a mixed crystal as claimed claim 1 comprising the step of reacting 1 mol of a succinic diester with 2 mol of the mixture of nitriles A-CN and B—CN in a molar ratio of 90:10 to 30:70 between the A-CN and B—CN in the mixture of nitriles, in an organic solvent, in the presence of a strong base and at elevated temperature to form a pigment alkali salt, hydrolysis of the pigment alkali salt in water, alcohol or both to obtain the mixed crystal and optionally solvent finishing.
7. A pigmented macromolecular organic material of natural or synthetic origin pigmented by a mixed crystal as claimed in claim 1 .
8. The macromolecular material of natural or synthetic origin as claimed in claimed 7 , wherein the macromolecular material of natural or synthetic origin is selected from the group consisting of plastics, resins, coatings, paints, printing inks, electrophotographic toners, electrophotographic developers, color filters and liquid inks.
9. A pigmented color filter, metallic coating or inkjet ink pigmented by a mixed crystal as claimed in claim 1 .