The chemical microstructure of acrylonitrile-pentyl methacrylate (A-P) copolymers prepared by photopolymerization using uranyl ion as the photo sensitizer is analyzed by 13 C{ 1 H} nuclear magnetic resonance spectroscopy. The composition of the copolymers were determined by elemental analysis, and c
Sequencing of N-vinyl-2-pyrrolidone/glycidyl methacrylate copolymers by one-dimensional and two-dimensional nuclear magnetic resonance spectroscopy
✍ Scribed by A. S. Brar; Rajeev Kumar
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 317 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Abstract
Copolymers of N‐vinyl‐2‐pyrrolidone (V) and glycidyl methacrylate (G) monomers of different compositions were prepared by free‐radical solution polymerization. The copolymer composition of these copolymers was determined with ^1^H‐NMR spectra. The reactivity ratios calculated from the Kelen–Tudos and nonlinear least‐square error‐in‐variable methods were r~V~ = 0.03 ± 0.01 and r~G~ = 5.05 ± 0.84 and r~V~ = 0.02 and r~G~ = 4.72, respectively. The triad sequence distribution in terms of V and G centered triads was determined from ^13^C{^1^H}‐NMR spectroscopy. The complete spectral assignment of ^13^C{^1^H}‐ and ^1^H‐NMR spectra was performed with the help of distortionless enhancement by polarization transfer and two‐dimensional ^13^C–^1^H heteronuclear single quantum coherence. The ^1^H–^1^H couplings were explained with total correlation spectroscopy and nuclear Overhauser enhancement spectroscopy spectra. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 50–60, 2002; DOI 10.1002/app.10186
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Copolymers containing acrylamide (A) and acrylonitrile (B) units of different compositions were synthesized by free-radical solution polymerization. The reactivity ratios were estimated by the Kelen Tudos and nonlinear error-in-variable methods. The triad sequence distribution in terms of A-and B-ce