The synthesis of a new diamine monomer, N-n-butyl 3,12-diamino-5,6,9,10tetrahydro[5]helicene-7,8-dicarboxylic imide (4), that contains a helically locked, Ushaped 4ะ,4ะ-o-terphenyl moiety is described. The monomer was polymerized with 3,3ะ,4,4ะ-oxydiphthalic dianhydride and 2,2-bis[4-(4-aminophenoxy
Poly(aryl ether)s containing o-terphenyl subunits. II. Random poly(ether sulfone)s
โ Scribed by Sean M. Mackinnon; Timothy P. Bender; Zhi Yuan Wang
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 219 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
The synthesis of a new A 2 X-type difluoride monomer, N-2-pyridyl-4ะ,4ะ-bis-(4-fluorobenzenesulfonyl)-o-terphenyl-3,6-dimethyl-4,5-dicarboxylic imide (3), is described. The monomer 3 was incorporated into a series of copoly(aryl ether sulfone)s by polymerization of 4,4ะ-isopropylidenediphenol and 4,4ะ-difluorophenylsulfone. The incorporation of monomer 3 had an observable effect on both the glass-transition temperature of poly(aryl ether sulfone)s and the tendency for macrocyclic oligomers to form during polymerization. Replacement of the pyridyl imide group via a transimidization reaction with propargyl amine proceeded quantitatively and without polymer degradation. The acetylene containing copoly(aryl ether sulfone) could be crosslinked by simple thermal treatment, resulting in an increase in the glass-transition temperature and solvent resistance.
๐ SIMILAR VOLUMES
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Three series of poly(aryl ether sulfone)s (PAESs) containing the phthalazinone moiety in the polymer backbone were synthesized by solution polycondensation of bis(4-chlorophenyl) sulfone with three commercial bisphenols and 4-(4-hydroxyphenyl)-2,3-phthalazin-1-one. Bisphenol-A, hydroquinone, and bis
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