Abstract

A new series of optically active and thermally stable poly(amide-imide)s (PAIs) with good inherent viscosities based on bicyclo diacids and etheric diamine in the main chain were synthesized from the direct polycondensation reaction of N,N΄-(bicyclo[2,2,2]oct-7-ene-tetracarboxylic)-bis-l-amino acids 3a-g with 1,2-Bis[4-aminophenoxy]ethane 7 by direct polycondensatios with two different media such as direct polycondensation in a medium consisting of n-methyl-2pyrrolidone (NMP)/triphenyl phosphite (TPP)/calcium chloride (CaCl 2 )/pyridine (Py) and direct polycondensation in a tosyl chloride (TsCl)/pyridine (Py)/n,ndimethylformamide (DMF) system. Also 3a-g were synthesized by the condensation reaction of bicyclo[2,2,2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride 1 with two equimolars of various amino acids such as l-alanine 2a, l-valine 2b, l-leucine 2c, l-isoleucine 2d, l-phenylalanine 2e, l-2-aminobutyric acid 2f and l-histidine 2g in an acetic acid solution. The polymerization reactions produced a series of thermally stable and optically active organosoluble PAIs. The resulting polymers were fully characterized by means of FT-IR and 1H-NMR spectroscopy, elemental analyses, inherent viscosity, specific rotation, solubility tests and differential scanning calorimeter (DSC). Also thermal properties of the PAIs 8a-g were investigated using thermal gravimetric analysis (TGA) and derivative of thermaogravimetric (DTG) analysis. Key word: Thermal properties; Optically active; Organosoluble; Poly(amide-imide)

Full Text
Paper version not known

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 call

Disclaimer: 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.