Polyimides of different structures were synthesized by reaction of 1,4phenylene diisocyanate (PPDI) and 1,5-naphthalene diisocyanate (NDI) with pyromellitic dianhydride (PMDA) and 3,3Π,4,4Π-benzophenonetetracarboxylic dianhydride (BTDA). Polyamide-imides were also prepared by reaction of PPDI and ND
Preparation and properties of novel processable polyimides derived from a new diisocyanate
β Scribed by Hamid Yeganeh; Shahram Mehdipour-Ataei
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 98 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
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## SYNOPSIS New polyimides containing diamantane units were prepared by a conventional two-step method starting from 1,6-diaminodiamantane and aromatic dianhydrides. The intermediate poly(amic acid)s had inherent viscosities of 0.33-0.55 dL/g. These polyimides did not decompose below 400Β°C in air
Two diisocyanate monomers containing methylene groups and built-in imide structure have been prepared from the parent diacids via the CurtiusΒ±Weinstock rearrangement. Polyimides have been synthesized by solution polymerization of these isocyanates with pyromellitic dianhydride (PMDA), 3,3',4,4'-benz
A series of aromatic diamines containing pendent methoxy, phenoxy, and biphenoxy moieties were synthesized. By the reaction of diamines with 3,3,4,4-benzophenonetetracarboxylic dianhydride (BTDA), several kinds of polyimides having bulky pendent ether groups were synthesized. Thermal properties and