𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Studies on the microstructure of poly(phenyl glycidyl ether) using the 13C nuclear magnetic resonance technique

✍ Scribed by Joan Carles Ronda; Angels Serra; Ana Mantecón; Virginia Cádiz


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
797 KB
Volume
36
Category
Article
ISSN
0032-3861

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


End-group analysis of poly(phenyl glycid
✍ Joan Carles Ronda; Angels Serra; Ana Mantecón; Virginia Cádiz 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 546 KB

## 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 glycid
✍ Joan Carles Ronda; Angels Serra; Ana Mantecón; Virginia Cádiz 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 519 KB

## 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

End-group analysis of poly(phenyl glycid
✍ Joan Carles Ronda; Angels Serra; Ana Mantecón; Virginia Cádiz 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 408 KB

## 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 han

Study of the characterization and curing
✍ Vernon M. Russell; Jack L. Koenig; Hong Yee Low; H. Ishida 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB 👁 2 views

Benzoxazines derived from bisphenol-A, formaldehyde, and primary amines were characterized using 13 C solid-state NMR spectroscopy. The two 1,3benzoxazines studied in this work are 2,2Ј-(3-methyl-4-dihydro-1,3,2-benzoxazine)propane, (B-m) and 2,2Ј-(3-phenyl-4-dihydro-1,3,2-benzoxazine)propane (B-a).