Abstract
The new pyrazole-ring containing diamine monomer with amino and cyano groups, 1,3-di-p-aminophenyl-4-cyano-5-aminopyrazole (PYA), was prepared from 4-nitrobenzoyl chloride and 4-nitrophenyl hydrazine with 4 steps. The monomer was converted to polyamides with terephthaloyl chloride and isophthaloyl chloride. The amino and cyano groups on the pyrazole-ring were not affected during polymerization. The synthesized polyamides having intrinsic viscosities of 0.92–1.18 dL/g were amorphous, and soluble in polar aprotic solvents and boiling acetone and THF. The polymers had high glass transition temperatures and high thermal stability. 5% weight loss temperatures in nitrogen occurred around 490°C, but these polymers are partially degraded at 300°C in air due to the amino group on the pyrazole-ring.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
