The cross-polarization dynamics between 1 H and 19 F in a Viton-type fluoroelastomer were studied using 19 F magic angle spinning (MAS) and 1 H ! 19 F cross-polarization (CP)/MAS NMR at 188.29 MHz. The phenomenological theory of spin thermodynamics based on the spin temperature hypothesis was employ
Fluorine-19 MAS and 1H→19F CP/MAS NMR studies of Viton fluoropolymers
✍ Scribed by Gustavo A. Monti; Robin K. Harris
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 191 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Fluorine-19M1HN nuclear magnetic resonance (NMR) at 188.29 MHz, including 1H ] 19FM1HN crosspolarization (CP) with high-speed magic-angle spinning (MAS), was used to study some Ñuoropolymers of the Viton type. The systems examined were (a) copolymers of vinylidene Ñuoride and hexaÑuoropropene and (b) terpolymers of vinylidene Ñuoride, tetraÑuoroethene and hexaÑuoropropene. Both commercial and specially prepared samples were used. Di †erent 1H ] 19FM1HN CP/MAS experiments were applied to study the relaxation of the polymers. The results are discussed in terms of the CP dynamics, using parametrized equations.
📜 SIMILAR VOLUMES
1998 magnetic resonance, nuclear quadrupole resonance magnetic resonance, nuclear quadrupole resonance (solids and liquids) D 6560 20 -014 1-and 2-D 19 F MAS NMR Study of Fluoride-Ion Mobility in α-PbF 2 . -The local motion of F-ions α-PbF 2 and K-doped α-PbF 2 is probed by 19 F MAS NMR collected a
## 13 C cross-polarization magic angle spinning NMR data are reported for eight derivatives of 4-arylhexahydro-1H,3H-pyrido[1,2-c]pyrimidine-1,3-diones 1-8 and the x-ray diffraction data for 4 with R = 4'-Me. The crystal structure of 4 shows the formation of centrosymmetric dimers via intermolecul
The four isomeric diÑuoro-2,11-dithia [ 3.3 ] paracyclophanes, with one Ñuorine substituent per aromatic ring 3F 2 , were prepared as a 1 :1 :1 :1 mixture. They were converted into the bissulphones, which were pyrolysed to yield the ar,arº-diÑuoro [ 2.2 ] paracyclophanes, as a mixture of pseudogemin