## Abstract Splittings in the ^13^C cross‐polarization magic angle spinning spectra of 1, 4‐dibromobenzene and 4‐bromo‐3, 5‐dimethylpyrazole are reported. They arise from (^79,81^Br, ^13^C) interactions influenced by the quadrupolar nature of the bromine nuclei. They are analysed using both ‘invers
Quantitation of intermolecular dipolar effects in NMR spectroscopy and high order MSE MR imaging
✍ Scribed by Chen, Z
- Publisher
- Springer
- Year
- 2000
- Tongue
- English
- Weight
- 160 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0968-5243
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✦ Synopsis
An analytical expression for intermolecular dipolar effects was derived for the CRAZED sequence with an arbitrary flip angle of the second RF pulse and time-varying gradients. A combination of the demagnetizing field theory and product operator formalism was utilized in the derivation. It is demonstrated that the time-averaged, not instantaneous, orientation of the applied gradients determines the contributions of long-range intermolecular dipole effects. An imaging sequence to detect intermolecular dipolar effects was designed. The second-and third-order multiple spin echo (MSE) NMR signals of swine muscle were observed and were found to be in good agreement with the theoretical predictions. MSE images of a water phantom with nth orders (n = -2, -3, -4, and -5) were also obtained, and their relative signal intensities and optimized TE values were elucidated and compared with the theoretical prediction.
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