Soluble polyimides were synthesized and characterized from two diamines and four dianhydrides by the two-and the one-step method. Most of the polyimides could be soluble by one-step method except β£,β£Π-bis(4-aminophenyl)-1,4-diisopropyl benzene/3,3Π,4,4Π-benzophenonetetracarboxylic dianhydride system
Synthesis and characterization of new soluble and thermostable polyimides via novel diisocyanates
β Scribed by Barikani, Mehdi; Yeganeh, Hamid; Ataei, Shahram Mehdipour
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 86 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0959-8103
No coin nor oath required. For personal study only.
β¦ Synopsis
A facile synthesis of two novel diisocyanates containing methylene groups and preformed imide structure is described. Furthermore, six thermally stable and soluble polyimides were synthesized by polycondensation of these two diisocyanates with pyromellitic dianhydride (PMDA), 3,3',4,4'-benzophenonetetracarboxylic dianhydride (BTDA) and hexaΒ―uoroisopropylidene-2,2-bis-(phthalic anhydride) (6FDA) in N,N-dimethyl acetamide. All monomers and polymers were characterized by conventional methods and their physical properties such as solution viscosity, solubility properties, thermal stability and thermal behaviour were studied.
π SIMILAR VOLUMES
A series of new soluble aromatic polyimides with inherent viscosities of 0.65-1.12 dL/g were synthesized from 1,3-bis(4-aminophenyl)-4,5-diphenylimidazolin-2-one and various aromatic tetracarboxylic dianhydrides by the conventional twostep procedure that included ring-opening polyaddition and subseq
New dianhydrides containing t-butyl and phenyl pendant groups have been synthesized and used as monomers, together with commercial diamines, to prepare novel polyimides. The influence of the chemical structure of the monomers on their reactivity has been studied by quantum semiempirical methods. The
An aqueous base-soluble polyimide (BAPAF/6FDA) was obtained from the polycondensation of 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane (BAPAF) and 4,4 -(hexafluoroisopropylidene) -bis(phthalic anhydride (6FDA). It exhibits high thermal stability and high transparency at 365 nm. A novel positive
Tetrachlorophthalic anhydride (1) was reacted with L-leucine (2) in toluene solution at refluxing temperature in the presence of triethylamine and the resulting imide-acid (4) was obtained in quantitative yield. The compound (4) was converted to the N-(tetrachlorophthaloyl)-L-leucine acid chloride (