## Abstract The hydroxylic end‐groups in the soluble fraction of poly(phenyl glycidyl ether) (PPGE) obtained with the aluminium isopropoxide (AIP)/ZnCl~2~ initiator system are studied using nuclear magnetic resonance spectroscopy (NMR). To achieve complete assignment, model compounds are synthesize
End-group analysis of poly(phenyl glycidyl ether), 2. Hydroxylic groups using 19F nuclear magnetic resonance
✍ Scribed by Joan Carles Ronda; Angels Serra; Ana Mantecón; Virginia Cádiz
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 408 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The hydroxylic end‐groups in the soluble fraction of poly(phenyl glycidyl ether) (PPGE) obtained with the aluminium isopropoxide (AIP)/ZnCl~2~ initiator system are studied using ^19^F NMR spectroscopy. Derivatization as trifluoroacetate esters affords poor structural information and handle difficulties. Hexafluoroacetone (HFA) hemiketalic adducts are much more easily prepared and offer more information, allowing not only to distinguish between primary and secondary alcohols but showing a clear sensitivity to the tacticity. This method is successful to calculate the percentage of hydroxylic end‐group in the polymer chain. In the case of an irregular PPGE sample, obtained with AIP alone as initiator, it is possible to identify three different hydroxylic end‐groups.
📜 SIMILAR VOLUMES
## Abstract Non‐hydroxylic end‐groups in the soluble fraction of poly(phenyl glycidyl ether) (PPGE) obtained with the aluminium isopropoxide (AIP)/ZnCl~2~ initiator system are studied using nuclear magnetic resonance (NMR) spectroscopy. To make assignments, model compounds are synthesized and sever