Synthesis of polyimides and segmented block copolyimides by transimidization

Citation
Tp. Bender et Zy. Wang, Synthesis of polyimides and segmented block copolyimides by transimidization, J POL SC PC, 38(21), 2000, pp. 3991-3996
Citations number
11
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
ISSN journal
0887624X → ACNP
Volume
38
Issue
21
Year of publication
2000
Pages
3991 - 3996
Database
ISI
SICI code
0887-624X(20001101)38:21<3991:SOPASB>2.0.ZU;2-M
Abstract
The transimidization reaction has been successfully utilized to prepare a s eries of segmented block copolyimides. The synthesis and polymerization of an AX-type amino imide monomer containing the tetrahydro[5]helicene unit we re accomplished. The AX-type amino imide monomer is stable during isolation and purification, owing to its inert X (e.g., N-pyridyl) group, but yet re adily underwent a self-transimidization reaction and produced polyimide. Be cause of the presence of two reactive ends, such an AX-type polyimide could be incorporated into a series of block copolyimides by reaction with comme rcially available dianhydrides and diamines. All the copolymers showed two distinct glass-transition temperatures, typically around 250 and 430 degree s C. (C) 2000 John Wiley & Sons, Inc.