| Abstract: | Unsaturated polyamides from methyl-fumaric (2-methyl-fumaric and 2.3-dimethyl-fumaric) acid dichlorides and diamines, i.e. 1.6-hexamethylenediamine, 1.10-decamethylenediamine, m-xylylenediamine, piperazine and trans-2.5-dimethylpiperazine were synthesized by low-temperature polycondensation. The polymer structures and properties were investigated by IR, X-ray, NMR, DSC, and TGA analyses. All polyamides were found to be soluble in several volatile organic solvents: furthermore – unlike polyamides derived from unsubstituted fumaric acid – polyamides from substituted fumaric acid derived from primary diamines showed melting or softening points. |
