## Abstract 1,2,5,6‐Tetraaminoanthraquinone has been condensed with isophthalaldehyde and terephthalaldehyde and their bisulfite addition compounds to yield new heat‐stable polymers. It has also been condensed with pyromellitic anhydride to give the pyrrolone. The highest viscosities were obtained
Polymers containing anthraquinone and quinoxaline units: Polypyrrolones
✍ Scribed by Dutt, Prabir K. ;Marvel, C. S.
- Book ID
- 104535507
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1970
- Tongue
- English
- Weight
- 405 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0449-296X
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✦ Synopsis
Abstract
Four ladder or partial ladder polypyrrolones containing anthraquinone recurring units have been synthesized by condensing the dianhydride of 1,2,5,6‐bis(α,β‐dicarboxyl‐pyrazino)anthraquinone with four different tetraamines, 1,2,4,5‐tetraaminobenzene tetrahydrochloride, 3,3′,4,4′‐tetraaminodiphenyl, 3,3′,4,4′‐tetraaminodiphenyl ether, and 1,2,5,6‐tetraaminoanthraquinone in dimethylacetamide and tetramethylene sulfone as reaction media. A prepolymer with an open structure was first formed which on further heating gave a closed‐ring structure. These polymers which were highly colored, powdery materials, were insoluble in common organic solvents and slightly soluble only in concentrated H~2~SO~4~. They could, however, be solubilized in alkali by reduction with sodium dithionite. These polymers with an inherent viscosity in the range of 0.2–0.5, showed good thermal stability.
📜 SIMILAR VOLUMES
## Abstract In an attempt to synthesize soluble polymers, diphenyl 1,5‐anthraquinonedicarboxylate was treated with 3,3′‐dimercaptobenzidine and 3,3′‐diaminobenzidine under various conditions. Although the ester reacted readily, side reactions prevented the formation of high molecular weight compoun
## Abstract A preparation for 1,2,5,6‐tetraaminoanthraquinone was worked out. The reactivity of this compound in nucleophilie substitutions and nucleophilic additions was studied. Polymers were made by condensation with pyromellitic anhydride, terephthaloyl chloride, and isophthaloyl chloride. The