Synthesis and properties of alternating copolyamide-imides based on 2,6-bis(4-aminophenoxy)naphthalene and comparison with its related isomeric polymers

Citation
Cp. Yang et al., Synthesis and properties of alternating copolyamide-imides based on 2,6-bis(4-aminophenoxy)naphthalene and comparison with its related isomeric polymers, J POL SC PC, 39(15), 2001, pp. 2591-2601
Citations number
31
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
ISSN journal
0887624X → ACNP
Volume
39
Issue
15
Year of publication
2001
Pages
2591 - 2601
Database
ISI
SICI code
0887-624X(20010801)39:15<2591:SAPOAC>2.0.ZU;2-9
Abstract
A series of novel polyamide-imides III containing 2,6-bis(phenoxy)naphthale ne units were synthesized by 2,6-bis(4-aminophenoxy)naphthalene and various bis(trimellitimide)s in N-methyl-2-pyrrolidone (NMP) using triphenyl phosp hite and pyridine as condensing agents through direct polycondensation. The polymers were obtained in quantitative yield with inherent viscosities up to 1.53 dL/g. Most of the polymers showed good solubility in NMP, N,N-dimet hylacetamide, N,N-dimethylformamide, and dimethyl sulfoxide and could be so lution-cast into transparent, flexible, and tough films. The films had tens ile strengths of 84-111 MPa, elongations at break of 8-33%, and initial mod uli of 2.2-2.8 GPa. Wide-angle X-ray diffraction revealed that most polymer s III were amorphous. The glass-transition temperatures of some of the poly mers could be determined by differential scanning calorimetry traces, recor ded at 247-290 degreesC. The polyamide-imides exhibited excellent thermal s tabilities and had 10% weight loss at temperatures in the range of 501-575 degreesC under nitrogen atmosphere. They left more than 57% residue even at 800 degreesC in nitrogen. A comparative study of some corresponding polyam ide-imides is also presented. (C) 2001 John Wiley & Sons, Inc.