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Heteronuclear Overhauser experiment

For compounds that contain a limited number of fluorine atoms, heteronuclear correlation spectroscopy experiments such as F H HETCOR and 2H-19F heteronuclear Overhauser enhancement spectroscopy (HOESY) can provide considerable assistance distinguishing structural isomers and diastereomers as well as for conformational analysis. HOESY experiments have been frequently used for conformational analysis of biomolecules containing fluorine labels.18... [Pg.45]

The HOESY (Heteronuclear Overhauser Effect Spectroscopy) experiment... [Pg.110]

Just as in the COSY type of experiments this cross-relaxation effect is not restricted to protons, but can also involve heteronuclei the acronym HOESY (heteronuclear Overhauser effect) is used in these cases. This can be used, for example, to show that an anion such as IT1., is in close proximity to the ligands of the organometallic compound, as was carried out by Macchioni et al. with a 19F-xH HOESY experiment [24]. [Pg.303]

An aspect of general interest in organometallic chemistry is the equilibrium between contact and solvent-separated ion pairs, because metal cations which are sun ounded by an individual solvent cage are expected to show different reactivity towards basic centres than those closely attached to carbanions or amines. At the same time, the anionic centre is less shielded in an SSIP than in a CIP and thus expected to be more reactive. In solution, the differentiation by NMR methods between both structural motifs relies in most cases on chemical shift interpretations and, if possible, on heteronuclear Overhauser (NOE) measurements. The latter method is especially powerful in the case of lithium organic compounds, where H, Li or even H, Li NOE can be detected by one- and two-dimensional experiments. ... [Pg.179]

Nuclei that undergo mutual relaxation via dipolar coupling are said to be dipolar coupled and give rise to the nuclear Overhauser effect. Whether the nuclei in question also may be scalar (or spin) coupled is not pertinent to the discussion (Section 5-4). NOE experiments can be either homonuclear or heteronuclear in nature, although the former, involving protons, are much more common. One-dimensional homonuclear Overhauser experiments are discussed in Section 7-3 their 2D versions, NOESY and ROESY, are treated in this section. [Pg.267]

To determine whether the catalyst remains in this conformation in solution, heteronuclear NOESY experiments were set up. If one of the ligands flips, nOe (nuclear Overhauser effect) contacts between the side chain protons and the phthaloyl carbons should be visible. No cross peaks were detected in the case of 20, meaning that the all-up conformation is also predominant in solution, whereas cross peaks in the spectrum of 19 indicated that the C4 symmetry is not maintained in solution. Variable temperature NMR experiments with 20 confirmed this, as the aromatic carbon atoms give rise to two singlets at room temperature, which merge into one broad singlet at higher temperatures (comparable to the spectmm of 19 at room temperature). [Pg.182]

Judeinstein et al have conducted direct measurement of through-space NMR interactions that provide definitive evidence for spatial proximity of different species. Dipole-dipole interactions can be measured in principle between any NMR active nuclei with heteronuclear correlation experiments in the liquid or solid state." The dipole-dipole interactions decay quickly with the internuclear distances (r ), and are difficult to evaluate for long-range distances and even more difficult when exchange, conformation, or motion phenomena are present. However, the measurement of the nuclear Overhauser method" based on the dipole-dipole-induced crossrelaxation, was proposed to successfully measure intermolecular interactions" and the formation of ion pairs." " In agreement with recent studies, the pulsed field gradient enhanced inverse HOESY (heteronuclear Overhauser enhancement spectroscopy) sequence is usually preferred because it is more sensitive for isotope pairs H- Li and also improves the digital resolution in the H crowded spectrum." ... [Pg.304]

LC-NMR plays a central role in the on-line identification of the constituents of crude plant extracts (Wolfender and others 2003). This technique alone, however, will not provide sufficient spectroscopic information for a complete identification of natural products, and other hyphenated methods, such as LC-UV-DAD and LC-MS/MS, are needed for providing complementary information. Added to this, LC-NMR experiments are time-consuming and have to be performed on the LC peak of interest, identified by prescreening with LC-UV-MS. NMR applied to phenolic compounds includes H NMR,13 C NMR, correlation spectroscopy (COSY), heteronuclear chemical shift correlation NMR (C-H HECTOR), nuclear Overhauser effect in the... [Pg.63]

The most important two-dimensional NMR experiments for solving stmctural problems are COSY (Correlation SpectroscopY), NOESY (Nuclear Overhauser Enhancement SpectroscopY), HSC (Heteronuclear Shift Correlation) and TOCSY (Total Correlation SpectroscopY). Most modem high-held NMR spectrometers have the capability to routinely and automatically acquire COSY, NOESY, HSC and TOCSY spectra. [Pg.80]


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See also in sourсe #XX -- [ Pg.7 ]




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