A novel bis(ether anhydride) monomer, 9,9-bis [4-(3,4-dicarboxyphenoxy)phenyl]fluorene dianhydride (4), was synthesized from the nitrodisplacement of 4-nitrophthalonitrile by the bisphenoxide ion of 9,9-bis(4-hydroxyphenyl)fluorene (1), followed by alkaline hydrolysis of the intermediate tetranitril
Synthesis and properties of new adamantane-based poly(ether imide)s
β Scribed by Sheng-Huei Hsiao; Ching-Tang Lee; Yaw-Terng Chern
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 186 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
A new adamantane-based bis(ether anhydride), 2,2-bis [4-(3,4-dicarboxyphenoxy)phenyl]adamantane dianhydride, was prepared in three steps starting from nitrodisplacement of 4-nitrophthalonitrile with the potassium phenolate of 2,2-bis(4hydroxyphenyl)adamantane. A series of adamantane-containing poly(ether imide)s were prepared from the adamantane-based bis(ether anhydride) and aromatic diamines by a conventional two-stage synthesis in which the poly(ether amic acid)s obtained in the first stage were heated stage-by-stage at 150 -270Β°C to give the poly-(ether imide)s. The intermediate poly(ether amic acid)s had inherent viscosities between 0.56 and 1.92 dL/g. Except for those from p-phenylenediamine, m-phenylenediamine, and benzidine, all the poly(ether amic acid) films could be thermally converted into transparent, flexible, and tough poly(ether imide) films. All the poly(ether imide)s showed limited solubility in organic solvents, although they were amorphous in nature as evidenced by X-ray diffractograms. Glass transition temperatures of these poly(ether imide)s were recorded in the range of 242-317Β°C by differential scanning calorimetry and of 270 -322Β°C by dynamic mechanical analysis. They exhibited high resistance to thermal degrdation, with 10% weight loss temperatures being recorded between 514 -538Β°C in nitrogen and 511-527Β°C in air.
π SIMILAR VOLUMES
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