Synthesis of new soluble aromatic poly(amide imide)s from unsymmetrical extended diamine containing phthalazinone moiety

✍ Scribed by Lin Cheng; Xi Gao Jian

• Publisher: John Wiley and Sons
• Year: 2004
• Tongue: English
• Weight: 78 KB
• Volume: 92
• Category: Article
• ISSN: 0021-8995
• DOI: 10.1002/app.20084

✦ Synopsis

Abstract

The preparation of a new unsymmetrical kink non‐coplanar heterocyclic diamine, 1,2‐dihydro‐2‐(4‐aminophenyl)‐4‐[4‐(3‐phenyl‐4‐aminophenoxy)phenyl]‐(2__H__)phthalazin‐1‐one (3), from a readily available unsymmetrical phthalazinone bisphenol‐like (1) was described. The diamine can be directly polymerized with various aromatic bis(trimellitimide)s (4a–e) by using triphenyl phosphite and pyridine as condensing agents to give a series of new aromatic poly(amide imides) (5a–e) containing the kink non‐coplanar phthalazinone heterocyclic units with inherent viscosities of 0.57–1.06 dL/g. The polymers were readily soluble in a variety of solvents such as N,N‐dimethylformamide, N,N‐dimethylacetamide, dimethylsulfoxide, N‐methyl‐2‐pyrrolidinone, and even in pyridine and m‐cresol and could be cast to form flexible and tough films. The glass transition temperatures were in the range of 315–340°C, and the temperatures for 5% weight loss in nitrogen were in the range of 487–512°C. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1516–1520, 2004