A new aromatic dicarboxylic acid, 1,4-bis(p-carboxyphenoxy)naphthyl (3), was synthesized by the reaction of p-fluorobenzonitrile with 1,4-naphthalenediol, followed by hydrolysis. Aromatic polyamides having inherent viscosities of 1.27-2.22 dL/ g were prepared by the triphenyl phosphite activated pol
Synthesis and properties of new polyarylates from 1,4-bis(4-carboxyphenoxy)naphthyl or 2,6-bis(4-carboxyphenoxy)naphthyl and various bisphenols
โ Scribed by Guey-Sheng Liou; Yaw-Terng Chern
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 153 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
New 1,4-naphthyl and 2,6-naphthyl-containing polyarylates having inherent viscosities up to 1.28 dL/g were synthesized by the high-temperature solution polycondensation from the acid chloride of 1,4-bis(4-carboxyphenoxy)naphthyl or 2,6bis(4-carboxyphenoxy)naphthyl and various bisphenols. Most of the resulting polyarylates showed amorphous characteristics and were readily soluble in common organic solvents such as N,N-dimethylacetamide (DMAc), N-methyl-2-pyrrolidone (NMP), ochlorophenol, and chloroform. Transparent, flexible, and colorless films of these polymers could be cast from the DMAc solutions. Their cast films had tensile strengths ranging from 54.9 to 84.2 MPa, elongations at break from 5.3% to 19.0%, and initial modulus from 2.0 to 2.8 GPa. These polymers had glass transition temperatures in the range of 172-280ยฐC and began to lose weight around 400ยฐC, with 10% weight loss being recorded at about 450ยฐC in air. Dynamic mechanical analysis (DMA) reveals that the polyarylates containing isopropylidene linkages have three transitions on the temperature scale between ฯช100 and 300ยฐC. However, only two transitions were observed in the other polyarylates without isoproylidene linkage.
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A new dicarboxylic acid monomer, 1,1-bis[4-(4-carboxyphenoxy)phenyl]-4tert-butylcyclohexane, bearing a pendent tert-butylcyclohexylidene group was prepared in three steps from 4-tert-butylcyclohexanone. The monomer was reacted with various diamines to produce a series of new polyamides with tripheny
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