Novel aromatic polyimides containing symmetric, bulky di-tert-butyl substituents unit were synthesized from 1,4-bis(4-aminophenoxy)2,5-di-tert-butylbenzene (BADTB) and various aromatic tetracarboxylic dianhydrides by the conventional twostage procedure that included ring-opening polyaddition in a po
Preparation and properties of novel processable polyimides derived from N,N-bis(isocyanatoalkyl)-1,2,4,5-benzenetetracarboxylic-1,2:4,5-diimides
β Scribed by Hamid Yeganeh; Mehdi Barikani
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 114 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
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'-benzophenonetetracarboxylic dianhydride (BTDA), and hexaΒ―uoroisopropylidene-2,2-bis(phthalic-anhydride) (6FDA).
All monomers and polymers were characterized by conventional methods, and the physical properties of the polymers, including solution viscosity, solubility, thermal stability and thermal behaviour, were studied.
π SIMILAR VOLUMES
Regioselective functionalization of 2,4,5,6-tetrachloro-1, 3-dicyanobenzene (TCDCB) by nucleophilic substitution of the chlorine at C(4) with L-Ala, L-Phe or L-Pro, followed by amide-bond formation to lipophilic amines containing strong pi-donor group, and by final introduction of the spacer 3-amino