The commercial poly(vinyl acetate) bulk was studied by nuclear magnetic resonance (NMR) at solution and solid state to understand much better the behavior of this polymer to obtain information on structure, sample molecular mobility, and heterogeneity. To analyze the behavior of this polymer, we hav
29Si nuclear magnetic resonance of poly(methylphenyl)silane
β Scribed by A-F de Mahieu; J. Devaux; C. Dereppe; G. Baudoux; J. Delhalle
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 497 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
β¦ Synopsis
A C1-terminated poly(methylpheny1)silane is synthesized and analyzed by "Si-NMR spectroscopy. Assignments are proposed for the different peaks observed. A modification of the chemical shifts of the peaks relative to the main chain atoms is observed upon heating. From these experimental results and computational calculations on model compounds, the assignments of the three main peaks to configurationally different Si atoms are confirmed.
π SIMILAR VOLUMES
Silicon-29 spin-lattice relaxation times and 29Si-(1H} nuclear Overhauser enhancements are reported for five trialkylsilanes and for sym-tetramethyldisiloxane, all of which contain a direct Si-H bond. Relaxation rate contributions from (Si, H) dipolar interactions and from other mechanisms are evalu
## Abstract ^13^C Nuclear magnetic resonance (NMR) spectra of atactic and syndiotacticβrich poly(methacrylonitrile) (PMAN) were determined. In addition, 2D (^1^Hβ^13^C COSY)COSY = COrrelated SpectroscopY. NMR spectra of Ξ±βmethyl and methylene regions of atactic PMAN were measured. Values of tetrad