Spin-echo, double-resonance (SEDOR) dipolar recoupling experiments are illustrated on an I = 1/2, S = 3/2 spin system for static and spinning samples. An 15 N-23 Na spin system is used to show that the simple pulse sequence is very effective in causing 15 N dipolar dephasing using either a 23 Na p/2
Internuclear Distance Determination of S=1, I=1/2 Spin Pairs Using REAPDOR NMR
β Scribed by Eric Hughes; Terry Gullion; Amir Goldbourt; Shimon Vega; Alexander J. Vega
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 214 KB
- Volume
- 156
- Category
- Article
- ISSN
- 1090-7807
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β¦ Synopsis
A universal function is proposed to describe REAPDOR dephasing curves of an observed spin-1/2 nucleus dipole-recoupled to a spin-1 quadrupolar nucleus ((2)H or (14)N). Previous work had shown that, in contrast to REDOR, the shape of the dephasing curve depends on a large number of parameters including the quadrupolar coupling constant and asymmetry parameter, the sample rotation speed, the RF amplitude, and the relative orientations of the quadrupole tensor and the internuclear vector. Here we demonstrate by numerical simulations that the actual dispersion of REAPDOR dephasing curves is quite small, provided the rotation speed and the RF amplitude applied to the quadrupolar nucleus satisfy an adiabaticity condition. The condition is easily met for (2)H and is also practically achievable for virtually any (14)N-containing compound. This allows the REAPDOR curves to be approximated by a simple universal gaussian-type function, comparison of which with experimental data yields internuclear distances with less than 4% error. The spin dynamics of the recoupling mechanism is discussed. The critical importance of a stable spinning speed for optimizing the signal-to-noise ratio of the (13)C echoes is demonstrated and practical suggestions for achieving high stability are presented. Examples of applications of the universal curve are given for (2)H/(13)C and (14)N/(13)C REAPDOR in alanine.
π SIMILAR VOLUMES
## Abstract It is demonstrated that in a case where neither the proton nor the naturalβabundance ^13^Cβsatellite 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.