Dipolar couplings, NMR

Structure of Solids - A H- H dipolar coupling NMR study of the water molecule in magnetically H dilute crystalline hydrates has been reported. High resolution F MAS and F- Cd REDOR NMR spectroscopy has been used to study oxygen/fluorine ordering in oxyfluorides. Solid-state N NMR spectroscopy has been used to investigate nitrosoarene-metal interactions in model systems and in haem proteins. Phase-alternated composite pulses have... 

Marathias VM, Tawa GJ, Goljer I, Bach II AC. Stereochemical Identification of R) and (5)-Ibuprofen Using Residual Dipolar Couplings, NMR, and Modeling. Chirality 2007 19 ... 

Molecular modeling is an indispensable tool in the determination of macromolecular structures from NMR data and in the interpretation of the data. Thus, state-of-the-art molecular dynamics simulations can reproduce relaxation data well [9,96] and supply a model of the motion in atomic detail. Qualitative aspects of correlated backbone motions can be understood from NMR structure ensembles [63]. Additional data, in particular residual dipolar couplings, improve the precision and accuracy of NMR structures qualitatively [12]. 

In addition to sample rotation, a particular solid state NMR experiment is further characterized by the pulse sequence used. As in solution NMR, a multitude of such sequences exist for solids many exploit through-space dipolar couplings for either signal enhancement, spectral assignment, interauclear distance determination or full correlation of the spectra of different nuclei. The most commonly applied solid state NMR experiments are concerned with the measurement of spectra in which intensities relate to the numbers of spins in different environments and the resonance frequencies are dominated by isotropic chemical shifts, much like NMR spectra of solutions. Even so, there is considerable room for useful elaboration the observed signal may be obtained by direct excitation, cross polarization from other nuclei or other means, and irradiation may be applied during observation or in echo periods prior to... 

Nuclear spins can be considered as dipoles that interact with each other via dipolar couplings. While this interaction leads to strongly broadened lines in soUd-state NMR spectroscopy, it is averaged out in isotropic solution due to the fast tumbUng of the solute molecules. In Uquid-state NMR spectroscopy, the dipolar interaction can only be observed indirectly by relaxation processes, where they represent the main source of longitudinal and transverse relaxation. 

K., Heckmann, D., Paululat, T., Kessler, H., Luy, B. Stretched poly(vinyl actetate) gels as NMR alignment media for the measurement of residual dipolar couplings in polar organic solvents. Angew. Chem. Int. Ed. 2005, 44,... 

Omger, M., Delaglio, F., Bax, A. Measurement of / and dipolar couplings from simplified two-dimensional NMR spectra./. Magn. Reson. 1998, 131, 373-378. 

S., Grzesiek, S., litman, B. J., Bax, A. Measurement of dipolar couplings in a transdudn peptide fragment weakly bound to oriented photo-activated rhodopsin. f. Biomol. NMR 2000, 16, 121-125. 

Rotational-echo double-resonance (REDOR)(75,79) is a new solid-state NMR technique which is sensitive to through-space carbon-nitrogen interactions between selectively 13C and 15N-enriched sites separated by up to 5A (20-22). The parameter directly measured in a REDOR experiment is the heteronuclear dipolar coupling constant DCN, which is in itself proportional to the inverse third power of the intemuclear distance, rCN. It is this dependence on (icn)3 which accounts both for REDOR s ability to accurately measure short distances and its insensitivity to longer-range interactions. As a technique which can probe, in detail, intermolecular interactions over a distance range of 5A, REDOR is well suited to studying the distribution of small selectively-labeled molecules in polymer delivery systems. 

Figure 2. Pulse sequence for 13C-serve REDOR NMR. This sequence differs from the original REDOR pulse sequence (ref. 18) in that n pulses alternate between 13C and 15N r.f channels. On alternate scans of the REDOR experiment, the 15N iz pulses are either applied or omitted. This figure illustrates that the REDOR pulse sequence with four rotor periods of 13C-15N dipolar-coupling evolution (Nc = 4) NC can be increased (in increments of two) by adding rotor periods and pairs of 13C and 15N n pulses between the end of the cross-polarization preparation and the start of data acquisition.

Olejniczak ET, Meadows RP, Wang H, Cai M, Nettesheim DG, Fesik SW. Improved NMR structures of protein/ligand complexes using residual dipolar couplings. J Am Chem Soc 1999 121 9249-9250. 

In the solid, dynamics occurring within the kHz frequency scale can be examined by line-shape analysis of 2H or 13C (or 15N) NMR spectra by respective quadrupolar and CSA interactions, isotropic peaks16,59-62 or dipolar couplings based on dipolar chemical shift correlation experiments.63-65 In the former, tyrosine or phenylalanine dynamics of Leu-enkephalin are examined at frequencies of 103-104 Hz by 2H NMR of deuterated samples and at 1.3 x 102 Hz by 13C CPMAS, respectively.60-62 In the latter, dipolar interactions between the 1H-1H and 1H-13C (or 3H-15N) pairs are determined by a 2D-MAS SLF technique such as wide-line separation (WISE)63 and dipolar chemical shift separation (DIP-SHIFT)64,65 or Lee-Goldburg CP (LGCP) NMR,66 respectively. In the WISE experiment, the XH wide-line spectrum of the blend polymers consists of a rather featureless superposition of components with different dipolar widths which can be separated in the second frequency dimension and related to structural units according to their 13C chemical shifts.63... 

The best and easiest way to implement such an experiment is to use adiabatic inversion pulses, in order to introduce heterogeneity for evolution under 13C-1H scalar or residual dipolar couplings by means of a frequency-swept 180° pulse on 13C that inverts 13C nuclei at different positions in the NMR sample at different times (Figure 13) 40,45 This filter is robust with respect to pulse miscalibration and operates efficiently without the need to cycle the phases of pulses that otherwise is a common feature of non-destructive LPJFs. 

Other exciting applications involved using parallel tempering in connection with available experimental data. For example, Falcioni and Deem [57] used X-ray data to refine structures of zeolites, and Haliloglu et al. [58] refined NMR structural data for proteins (in particular using residual dipolar coupling constraints). 

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