The effect of several new homonuclear dipolar decoupling methods (frequency-switching Lee-Goldburg decoupling and two sequences based on z-rotational decoupling) on the 13 C spectra of liquid crystals has been studied, and the results are compared with those obtained by using two well-established me
Combining PGSE NMR with Homonuclear Dipolar Decoupling
✍ Scribed by S.V Dvinskikh; I Furó
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 97 KB
- Volume
- 144
- Category
- Article
- ISSN
- 1090-7807
No coin nor oath required. For personal study only.
✦ Synopsis
A new robust approach for combining multiple-pulse homonuclear decoupling and PGSE NMR is introduced for accurately measuring molecular diffusion coefficients in systems with nonvanishing static homonuclear dipolar couplings. Homonuclear decoupling suppresses dipolar dephasing during the gradient pulses but its efficiency and scaling factor for the effective gradient vary across the sample because of the large variation of the frequency offset caused by the gradient. The resulting artifacts are reduced by introducing a slice selection scheme. The method is demonstrated by 19 F PGSE NMR experiments in a lyotropic liquid crystal.
📜 SIMILAR VOLUMES
A new PGSE NMR experiment, designed to measure molecular diffusion coefficients in systems with nonvanishing static dipolar coupling, is described. The fast static dipolar dephasing of the single-quantum 13 C coherences is removed by multiple-pulse heteronuclear decoupling. The resulting slow dephas
On the other hand, the resolution in the upfield region is not In this Communication, we demonstrate that the use of optimal, due to a combination of strong homonuclear dipolar frequency-switched Lee-Goldberg irradiation during the couplings and small shift dispersion for most aliphatic proproton ev
NMR methods (S. V. Dvinskikh et al., J. Magn. Reson. 142, 102-110 (2000) and S. V. Dvinskikh and I. Furó, J. Magn. Reson. 144, 142-149 (2000)) that combine PGSE with dipolar decoupling are extended to polycrystalline solids and unoriented liquid crystals. Decoupling suppresses dipolar dephasing not
## Abstract The ϕ angle in a cyclic peptide is determined by the combined use of homonuclear and heteronuclear coupling constants. Two of the four coupling constants that define the ϕ angle in a peptide are determined exactly, two qualitatively. Via Karplus‐type equations, they are transformed into
## Abstract It is demonstrated that in a case where neither the proton nor the natural‐abundance ^13^C‐satellite spectra of a partially oriented molecule carry enough structural information, one can determine the entire molecular geometry by the combined use of several liquid crystals as solvents.