For compounds giving "crowded" 1-dimensional magic-anglespinning spectra, information about the local atomic environment in the form of the chemical shift anisotropy (CSA) is sacrificed for high resolution of the less informative isotropic chemical shift. Magic-angle-turning (MAT) NMR pulse sequence
Fluorine-19 NMR of solids with both homonuclear (multipulse) decoupling and pulsed proton decoupling
โ Scribed by Ulrich Scheler; Robin K. Harris
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 328 KB
- Volume
- 262
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The application of multipulse and of combined rotation and multipulse spectroscopy (CRAMPS) to fluorine is demonstrated. The MREV-8 multipulse sequence is applied to average the homonuclear dipolar coupling between the fluorine nuclei. The heteronuclear dipolar coupling to the protons can be suppressed by irradiation with a synchronized sequence of "rr pulses at the proton frequency. MAS is applied to average the anisotropy of the chemical shift. Applications to a fluorinated adamantane derivative and to polyvinylidenedifluoride (PVDF) are shown.
๐ SIMILAR VOLUMES
## Abstract In crystalline polyoxymethylene, a system with tightly coupled protons, it is shown experimentally that the averaging of the dipolar local field of protons by multipulse proton homonuclear decoupling leads to a decrease in the spinโspin contribution to the ^13^C rotating frame relaxatio
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