## Abstract Summary: New hyperbranched poly(arylene ether amides) with fluorine or hydroxy end groups were synthesized from AB~2~ or A~2~B type monomers via a nucleophilic aromatic substitution (S~N~Ar) reaction. Monomer syntheses were facilitated by chemo‐selective amidation reactions, and even a
✦ LIBER ✦
Preparation of Poly(arylene ether pyrimidine)s by Aromatic Nucleophilic Substitution Reactions †
✍ Scribed by Herbert, C. G.; Bass, R. G.; Watson, K. A.; Connell, J. W.
- Book ID
- 126882635
- Publisher
- American Chemical Society
- Year
- 1996
- Tongue
- English
- Weight
- 349 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0024-9297
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## Abstract Summary: Poly(arylene ether amine)s were synthesized by a nucleophilic aromatic substitution polycondensation of bis[4‐fluoro‐3‐(trifluoromethyl)phenyl]amine with several bisphenols. Even though the monomer has an electron‐donating diphenylamine moiety, which normally deactivates a nucl