Polyamides containing s-triazine rings and fluorene “cardo”groups: synthesis and characterization
Two new polyamides containing s-triazine rings and fluorene “cardo” groups were synthesized by low temperature interfacial polycondensation of two s-triazine ring containing diacyl chlorides viz. 2,4-bis(4-chlorocarbonylphenoxy)-6-methoxy- s-triazine and 2,4-bis(3-chlorocarbonylphenoxy)-6-methoxy- s...
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Published in: | European polymer journal Vol. 37; no. 7; pp. 1493 - 1498 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford
Elsevier Ltd
01-07-2001
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | Two new polyamides containing
s-triazine rings and fluorene “cardo” groups were synthesized by low temperature interfacial polycondensation of two
s-triazine ring containing diacyl chlorides viz. 2,4-bis(4-chlorocarbonylphenoxy)-6-methoxy-
s-triazine and 2,4-bis(3-chlorocarbonylphenoxy)-6-methoxy-
s-triazine with a cardo diamine viz. 9,9-bis(4-aminophenyl) fluorene. The resulting polyamides were characterized by elemental analysis, viscosity measurements, X-ray diffraction studies, thermogravimetry and IR,
1
H- and
13
C-NMR spectroscopy. The polyamides PA-1 and PA-2 had inherent viscosity values 0.52 and 0.60 dl/g respectively in
N,
N-dimethylacetamide (DMAc) at 30°C. Both the polyamides were found to be readily soluble at room temperature in polar solvents such as dimethylsulfoxide, DMAc,
N,
N-dimethylformamide,
N-methyl-2-pyrrolidone and
m-cresol. Transparent, tough and flexible films of polyamides could be cast from DMAc solution. Thermogravimetric analysis of the polyamides indicated no weight loss below 360°C under nitrogen atmosphere. |
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ISSN: | 0014-3057 1873-1945 |
DOI: | 10.1016/S0014-3057(00)00194-4 |