Rotating frame SpectroscopY

ID, one-dimensional 2D, two-dimensional NOE, nuclear Overhauser effect ROESY, rotating-frame spectroscopy... 

Styles, R Rotating Frame Spectroscopy and Spectroscopy Imaging. Vol. 27, pp. 45-66 Ugurbil, K., see Garwood, M. 

Multidimensional spectraas well as techniques including DEPT (distortionless enhancement by polarization transfer), COSY (correlated spectroscopy), and ROESY (rotating-frame overhauser enhancement spectroscopy) have been increasingly used. 

ROESY Rotating-frame Overhauser enhancement spectroscopy... 

The conformation of the mixed p agonist/5 antagonist H-Tyr-c[-D-Orn-2-Nal-D-Pro-Gly-] in comparison to that of H-Tyr-c[-D-Orn-Phe-D-Pro-Gly-] was studied in DMSO-d6 by NMR spectroscopy and by molecular mechanics calculations [62,64]. Neither peptide showed nuclear Overhauser effects between C H protons or chemical exchange cross peaks in spectra obtained by total correlation and rotating frame Overhauser enhance-... 

In order to combat this, the rotating frame Overhauser effect spectroscopy (ROESY) techniques can be employed. An in-depth discussion of how this technique works is outside the remit of this book but suffice to say, in the ROESY methods (1- and 2-D), NOE data is acquired as if in a weak r.f. field rather than in a large, static magnetic field and this assures that all NOEs are present and positive, irrespective of tumbling rate and magnet size. It is possible that some TOCSY correlations can break through in ROESY spectra but these will have opposite phase to the genuine ROESY correlations and so should therefore not be a problem - unless they should overlap accidentally with them. A 2-D ROESY spectrum of the naphthalene compound is shown below (Spectrum 8.6). 

ROESY Rotating-frame Overhauser effect spectroscopy. A variation (one and two dimensional) on the nuclear Overhauser experiment (NOE). The techniques have the advantage of being applicable for all sizes of molecule. See Laboratory frame model. 

Sowinski and coworkers40 reported a structure of vacidin A (63), an aromatic hep-taene macrolide antibiotic. The constitution of vacidin A, a representative of the aromatic heptaene macrolide antibiotics, was established on the basis of 13C and H- H double quantum filtered correlated spectroscopy, rotating frame nuclear Overhauser effect spectroscopy, 7-resolved 11 as well as H-13C correlation NMR spectra. The geometry of the polyene chromophore was determined as 22E, 24E, 26E, 28Z, 30Z, 32E, 34E. 

The data from H NMR studies of 63, which included double quantum filtered phase sensitive correlated spectroscopy (DQF-COSY) and rotating frame nuclear Overhauser effect spectroscopy (ROESY) experiments (Figure 12), are collected in Table 17. 

Various studies were focusing on the conformational behavior of the cinchonan carbamate selectors in free and complexed form, which could readily be derived from the dihedral coupling constant of the Hs-Hg protons ( /hsh9) and intramolecular NOEs as measured by 2D-NOESY [92,93] or two-dimensional rotating frame Overhauser effect spectroscopy (2D-ROESY) [65] spectra. 

Whittemore, N.A. et al., A quenched molecular dynamics-rotating frame Overhauser spectroscopy study of a series of semibiosynthetically monoacylated anthocyanins, J. Org. Chem., 69, 1663, 2004. 

ROESY Rotating Frame Overhauser Effect SpectroscopY... 

ROESY rotating frame overhause effect spectroscopy... 

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