Rotational echo double resonance REDOR experiment

Accurate 13C-15N interatomic distances have been measured by means of rotational echo double resonance (REDOR) experiments for oligopeptides [50]. The interatomic 13C-15N distance in the hydrogen bonded fragment was measured to be 4.5 0.1 A in five different samples studied. This finding is consistent with an a-helix structure, in agreement with conformation-dependent 13C chemical shift data. 

Rotational-echo double resonance (REDOR) experiments follow another strategy to achieve recoupling of weak heteronuclear dipolar coupling interactions under MAS conditions, quite different from the approach. REDOR experiments prevent the refocusing of weak heteronuclear dipolar couphng interactions under MAS by applying rotation-synchronized trains of 7T pulses. Figure 9 depicts some (of many possible) versions of REDOR sequences. The theory of REDOR has been treated extensively in the literature. 

A series of ID and 2D NMR experiments performed on nanocomposites of hectorite, a smectite clay mineral, showed new opportunities for studying large assemblies of layered minerals with polymeric materials.In particular. rotational-echo double-resonance (REDOR) experiments afforded H- Si distances with precision, and a mobility gradient of intercalated polyethyleneoxide (PEG) segments was demonstrated in H-" Si wideline separation (WISE) experiments. 

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. 

Another study of the surface structure of CdSe NCs of 3.7 nm size used 31P MAS-NMR and 31P/77Se rotational-echo double-resonance (REDOR) to identify overlapping broad peaks from two surface species trioctylphosphine oxide (TOPO) at 29.3 ppm and trioctylphosphine selenide (TOPSe) at 22.2 ppm [343]. Both the isotropic chemical shift and CSA of the surface-bound TOPO were substantially different from those of the free ligand. Spin-echo experiments on 31P were stated to indicate an average P-P distance of 8-10 A at the surface, consistent with capping at alternate atomic sites (all Cd but not Se). 

Many multiple resonance methods such as cross-polarisation (CP), Rotational Echo Double Resonance (REDOR), and Transferred Echo Double Resonance (TEDOR) are available. Their application can be differentiated between systems involving exclusively spin- /2 nuclei and those containing quadrupolar nuclei. The presence of quadrupolar nuclei may prohibit straightforward application of these experiments and can affect the interpretation of the results. There are, however, benefits arising from the presence of quadrupolar nuclei, as illustrated by the Transfer of Populations by Double Resonance (TRAPDOR) experiment which will only work for quadrupolar nuclei. 

One of the important applications of butylcalix[4]arenes arises from their ability to trap alkali metal ions. In particular, Cs+-calixarene complexes have received much attention because of the need to remove the Cs radionucleotide from nuclear wastes. Benevelli et al. have used one-pulse solid state NMR experiments to directly observe Li, Na and Cs ions in the host cavity [52]. More advanced experiments, which allow the investigation of metal lattice interactions were also reported. Rotational-echo double resonance (REDOR) NMR is a useful tool for obtaining structural details of butylcalix[4]arene [53]. Gullion and coworkers used REDOR to determine the position of the... 

A rotational-echo, double-resonance (REDOR) 15N-I3C NMR experiment has been performed on an alanine co-crystallized from five-component alanines, isotopically enriched in l3C, 15N, or I3C.41-43 REDOR 15N-I3C NMR involves the dephasing of carbon magnetization by 15N 180° pulses synchronized with magic-angle spinning. The C-N dipolar coupling deter-... 

From the success of the cross-polarization experiments, one may predict success for a variety of related experiments that depend on the dipolar interaction (such as those of Veeman [951, where spin echoes are observed under magic-angle spinning and double resonance conditions). Further experiments that allow determination of internuclear distances should also be possible, including rotational-echo double-resonance (REDOR) NMR [96], and transferred-echo double-resonance (TEDOR) NMR [97], the latter being related to INEPT experiments in liquids. 

Having demonstrated the achievement of high-resolution sohd state NMR capability, the authors describe experiments that combine the high-resolution aspect of MAS NMR with methods that retain the structure and/or dynamic information inherent in the anisotropic interactions. Rotational-echo double resonance (REDOR) allows the determination of D between isolated heteronuclear spin pairs. D is related simply and without approximation to intemuclear separation. Hence, REDOR makes possible the unambiguous direct determination of intemuclear distance between the labeled spin pair, independent of pair orientation, i. e., in amorphous and /or microaystaUine solids, and extends our abihty to quantitatively explore complex materials. It is also possible to extract intemuclear distance from homonuclear dipolar coupled spin pairs, and these experiments are also reviewed. 

In the rotational-echo double-resonance (REDOR) [60—62] technique, the distance between two heteronuclei is determined by comparing the signal intensity in two closely related experiments. The interpretation of the experimental results assumes the existence of isolated spin pairs, and there is thus usually a requirement for selective isotopic labelling at the two sites, the distance between which is of interest. 

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