This work explores the utility of simple rotary resonance experiments for the determination of the magnitude and orientation of 13 C chemical shift tensors relative to one or more 13 C-14 N internuclear axes from 13 C magic-angle-spinning NMR experiments. The experiment relies on simultaneous recoup
NMR chemical shift anisotropy measurements by RF driven rotary resonance
โ Scribed by Zhehong Gan; David M. Grant; R.R. Ernst
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 527 KB
- Volume
- 254
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
A rotary resonant effect in magic angle sample spinning NMR experiments occurs when the magnitude of an applied radio frequency field matches a multiple of the spinning frequency. The modulated anisotropic chemical shift drives the rotary resonance. Based on this effect, a two-dimensional experiment is introduced to correlate the isotropic chemical shift and the chemical shift anisotropy. Experimental results are compared with computer simulations based on average Hamiltonian theory and Floquet theory of rotary resonance, An experimental scheme is introduced for creating rotary resonance echoes,
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A solid state NMR technique for the determination of peptide backbone conformations at specific sites in unoriented samples under magic angle spinning (MAS) is described and demonstrated on a doubly labeled polycrystalline sample of the tripeptide AlaGlyGly and a sextuply labeled lyophilized sample
NMR methods (S. V. Dvinskikh et al., J. Magn. Reson. 142, 102-110 (2000) and S. V. Dvinskikh and I. Furรณ, 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