## Abstract New poly(aryl ether ketone) and poly(aryl ether sulfone) monodisperse model oligomers were synthesized in good yield via nucleophilic reactions. They were characterized by means of ^1^H and ^13^C NMR spectroscopy, and all chemical shifts were assigned to the corresponding nuclei. Both p
A novel synthesis and characterization of phenylacetylene end-capped poly(aryl ether sulfone) and poly(aryl ether ketone) oligomers
✍ Scribed by Mathew Kozuch; Angela Schaffer; Atul Bhatnagar; Stanley Phulpagar; Dillip K. Mohanty
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 582 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
A series of controlled molecular weight poly(aryl ether sulfone) oligomers with benzophenone moieties at the chain termini were prepared. The two carbonyl groups at the chain ends were converted to ethynyl groups by using trimethylsilyldiazomethane/BuLi in tetrahydrofuran. Reactions of 4,4′‐isopropylidenediphenol with 4,4′‐difluorobenzophenone and 4‐fluorophenylphenylacetylene as the end‐capping reagent in N,N‐dimelthylacetamide afforded the desired poly(aryl ether ketone) oligomers Both sulfone and ketone containing oligomeric polyethers undergo crosslinking reactions at elevated temperatures.
📜 SIMILAR VOLUMES
Poly(ether sulfone) and poly(ether sulfone ketone) copolymers (I-V) were synthesized by the nucleophilic substitution reaction of 4,4Ј-dihydroxy diphenyl sulfone (DHDPS, A) with various mole proportions 4,4Ј-difluoro benzophenone (DFBP, B) and 4,4Ј-difluoro diphenyl sulfone (DFDPS, C) using sulfolan