This work synthesized a series of new polyamides by direct polycondensation of 1,3-bis[4-(4-carboxyphenoxy)phenyl]adamantane ( I) with various diamines. The diacid I was synthesized from 1,3-bis(4-hydroxyphenyl)adamantane in two steps. Polyamides III were soluble in N-methyl-2-pyrrolidone (NMP), N,N
Synthesis and characterization of tough polycyclic polyamides containing 4,9-Diamantyl moieties in the main chain
β Scribed by Yaw-Terng Chern; Wen-Liang Wang
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 680 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
A series of new polyamides were synthesized by direct polycondensation of the 4,9-diamantane dicarboxylic acid (I) with various aromatic diamines in N-methyl-2-pyrrolidone (NMP) containing lithium chloride. The polyamides had inherent viscosities of 0.56-1.85 dL/g. Dynamic mechanical analysis revealed the polymers IIIa-IIId to have main melting transitions at 403,431, 423, and 452"C, respectively. Moreover, these polymers were quite stable at high temperatures and maintained good mechanical properties (G' = ca. lo8 Pa) up to temperatures close to the main transition well above 400Β°C. Although the polyamides contained rigid 4,9-diamantyl moieties in the main chain, the tensile properties of the polyamides showed toughness. Elongations of polyamides IIIa and IIIb reached 38.3 and 31.7%, respectively, before breaking. A glass transition was not observed. However, polyamide IIIc shows a melting transition with a sharp endothermic peak at 423Β°C by DSC measurement. Additionally, the introduction of 4,9-diamantyl units into the polyamide backbone resulted in polyamides with high thermal stability and good mechanical properties.
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