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 2,2Π-(3-methyl-4-dihydro-1,3,2-benzoxazine)propane, (B-m) and 2,2Π-(3-phenyl-4-dihydro-1,3,2-benzoxazine)propane (B-a).
Study of the characterization and curing of a phenyl benzoxazine using 15N solid-state nuclear magnetic resonance spectroscopy
β Scribed by Vernon M. Russell; Jack L. Koenig; Hong Yee Low; Hatsuo Ishida
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 266 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
A difunctional 1,3-benzoxazine compound, 2,2Π-(3-phenyl-4-dihydro-1,3,2benzoxazine)propane (B-a), derived from bisphenol-A, 15 N-enriched aniline, and formaldehyde was synthesized and characterized using 15 N-NMR and 13 C-NMR spectroscopies. The observed resonances in the solid-state 15 N-and 13 C-NMR spectra showed good agreement with the calculated chemical shifts which are based on the chemical structure. The B-a samples were cured at 150 and 200Β°C. The polymerization inspired peak intensity changes and line-width broadenings in the NMR spectra.
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