A novel polyaryloxydiphenylsilane was synthesized successfully by solution polycondensation of 2,2Ј-dimethyl-biphenyl-4,4Ј-diol with diphenyldichlorosilane and the catalyst triethylamine in toluene at 80 °C. Polymers with a relatively high inherent viscosity and yield were obtained when the reaction
Synthesis and characterization of novel polyaspartimides derived from 2,2′-dimethyl-4,4′-bis(4-maleimidophenoxy)biphenyl and various diamines
✍ Scribed by Der-Jang Liaw; Daniel Chun-Hung Liu; Been-Yang Liaw; Tong-Ing Ho
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 198 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
A novel bismaleimide, 2,2Ј-dimethyl-4,4Ј-bis(4-maleimidophenoxy)biphenyl, containing noncoplanar 2,2Ј-dimethylbiphenylene and flexible ether units in the polymer backbone was synthesized from 2,2Ј-dimethyl-4,4Ј-bis(4-aminophenoxy)biphenyl with maleic anhydride. The bismaleimide was reacted with 11 diamines using m-cresol as a solvent and glacial acetic acid as a catalyst to produce novel polyaspartimides. Polymers were identified by elemental analysis and infrared spectroscopy, and characterized by solubility test, X-ray diffraction, and thermal analysis (differential scanning calorimetry and thermogravimetric analysis). The inherent viscosities of the polymers varied from 0.22 to 0.48 dL g Ϫ1 in concentration of 1.0 g dL Ϫ1 of N,Ndimethylformamide. All polymers are soluble in N-methyl-2-pyrrolidone, N,N-dimethylacetamide, N,N-dimethylformamide, dimethylsulfoxide, pyridine, m-cresol, and tetrahydrofuran. The polymers, except PASI-4, had moderate glass transition temperature in the range of 188°-226°C and good thermo-oxidative stability, losing 10% mass in the range of 375°-426°C in air and 357°-415°C in nitrogen.
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