2,6-Bis(4-aminophenoxy)naphthalene (2,6-BAPON) was synthesized in two steps from the condensation of 2,6-dihydroxynaphthalene with p-chloronitrobenzene in the presence of potassium carbonate, giving 2,6-bis(4-nitrophenoxy)naphthalene, followed by hydrazine hydrate/Pd-C reduction. A series of new pol
Synthesis and characterization of wholly aromatic polyesters derived from 1-phenyl-2,6-naphthalene-dicarboxylic acid and aromatic diols
β Scribed by Sung-Jae Chung; Seung-Moo Huh; Jung-Il Jin
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 694 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
A series of new wholly aromatic polyesters was synthesized by melt polycondensation of 1-phenyl-2,6-naphthalenedicarboxylic acid (PNDA) and &acetates of various aromatic diols. The aromatic diols studied are hydroquinone (HQ), methylhydroquinone (MHQ), phenylhydroquinone (PHQ), (a-phenylisopropy1)hydroquinone (PIHQ), 2,6-naphthalenediol (2,6-ND), 1,4-naphthalenediol (1,4-ND), and 4,4'-hiphenol (BP). These polyesters were characterized for their crystallinity, glass transition temperature ( Tg), melting temperature (T,,J, liquid crystallinity, and thermal stability. In general, crystallinity of the polyesters are very low and the Tg values of the polyesters range from 150 to 172Β°C depending on the structure of aromatic diols. All of the polymers formed nematic phases above their T,,, or T,-The polyesters derived from PHQ and PIHQ are soluble in chlorinated hydrocarbon solvents. The initial decomposition temperatures of the polyesters are above 400Β°C under N2 atmosphere.
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