## Abstract A novel class of polyamide‐quinazolinediones was synthesized by the polymerization of 2,2′‐disubstituted bis(1,3,4‐oxadiazolin‐5‐ones) with aromatic bis‐__o__‐amino esters in __m__‐cresol. The polymerization probably proceeded in the formation of ring‐opening adducts, which in turn were
Synthesis of aromatic polythioamide-oxothioxoquinazolines from bis(1,3,4-thiadiazoline-5-thione) and aromatic bis-o-amino esters
✍ Scribed by Saegusa, Yasuo ;Iida, Sakayu ;Nakamura, Shigeo ;Chau, Nguyen ;Iwakura, Yoshio
- Publisher
- John Wiley and Sons
- Year
- 1984
- Weight
- 346 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0360-6376
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✦ Synopsis
Abstract
Aromatic polythioamide‐oxothioxoquinazolines were synthesized by the polycondensation of 2,2′‐(m‐phenylene)bis‐1,3,4‐thiadiazoline‐5‐thione with aromatic bis‐o‐amino esters. The polymerizations were carried out at 160°C in acidic media such as m‐cresol, sulfolane, and polyphosphoric acid to produce polymers with reduced viscosities up to 0.5 dL/g. These polymers were soluble in polar aprotic solvents like N‐methyl‐2‐pyrrolidone and some acidic media including m‐cresol. The polythioamide‐oxothioxoquinazolines showed relatively good thermal stability with 10% weight loss at 344–394°C in air.
📜 SIMILAR VOLUMES
Aromatic tetracarboxylic dianhydride having crank and twisted noncoplanar structure, 2,2 -bis(3,4-dicarboxyphenoxy)-1,1 -binaphthyl dianhydride, was synthesized by the reaction of 4-nitrophthalonitrile with 2,2 -dihydroxy-1,1 -binaphthyl, followed by alkaline hydrolysis of the intermediate bis(ether