Metathesis polymerization of N-aryl norbornene dicarboximides. I
β Scribed by Rajni Madan; R. C. Anand; Indra K. Varma
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 185 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
Metathesis polymerization of N-phenyl-exo-norbornene dicarboximide and ortho/meta/para methyl substituted phenyl nadimides was carried out using WCl 6 / tetramethyltin. Structural characterization was done by FTIR, 1 H-and 13 C-NMR. A mixture of cis and trans double bond structures were introduced in the backbone during polymerization. The cis content was higher (52 to 65%). In the DSC scan of poly( N-otolyl nadimide), two exotherms were observed at 240 and 270ΠC while in other samples only one exothermic transition was observed above 240ΠC. These exotherms disappeared in the second heating cycle. The T g of the polymers, as determined in the second heating cycle, was highest in poly( N-o-tolyl nadimide) and lowest in poly( N-m-tolyl nadimide). The polymers were stable up to 443 { 3ΠC and decomposed above this temperature in a single step.
π SIMILAR VOLUMES
Figure 8. FTIR spectra of: (a) XQ(T), (b) PXQ.
The article deals with synthesis, characterization, and polymerization of 5norbornene-2,3-dicarboximide end-capped resins (bisnadimides) based on 4,4diaminodiphenylether, 1,4/1,3-bis(4 -aminophenoxy) benzene, 2,2 -bis[4-(4-aminophenoxy)phenyl]propane, and bis[4-(4 -aminophenoxy)phenyl]sulphone. Both