Curing chemistry of phenylethynyl-terminated imide oligomers: Synthesis ofC-13-labeled oligomers and solid-state NMR studies

Citation
Cc. Roberts et al., Curing chemistry of phenylethynyl-terminated imide oligomers: Synthesis ofC-13-labeled oligomers and solid-state NMR studies, J POL SC PC, 38(19), 2000, pp. 3486-3497
Citations number
47
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
ISSN journal
0887624X → ACNP
Volume
38
Issue
19
Year of publication
2000
Pages
3486 - 3497
Database
ISI
SICI code
0887-624X(20001001)38:19<3486:CCOPIO>2.0.ZU;2-L
Abstract
4-(Phenylethynyl-alpha,beta-C-13)phthalic anhydride (PEPA) and C-13-labeled phenylethynyl-terminated imide (PETI) oligomers were synthesized, and soli d-state C-13 nuclear magnetic resonance (NMR) spectroscopy was used to dete rmine the structure of cured oligomers. Solid-state C-13 NMR spectra were c ollected before and after thermal curing. Using solid-state C-13 NMR differ ence spectroscopy, several cure products were identified. The observed C-13 NMR resonances were assigned to four different classes of cure products: a romatics, products from backbone addition (substituted stilbenes and tetrap henylethanes), polyenes, and cyclobutadiene cyclodimers. The effects of pos tcuring and oligomer chain length on the structure of the cured resins were examined. (C) 2000 John Wiley & Sons, Inc.