Nuclear Overhauser effect homonuclear

Since the discovery of the nuclear Overhauser effect (NOE, see previous section) [4, 5] and scalar coupling constants [36, 37] decades ago, NMR-derived structure calculations of biomolecules largely depended on the measurement of these two parameters [38]. Recently it became possible to use cross-correlated relaxation (CCR) to directly measure angles between bond vectors [39] (see also Chapt 7). In addition, residual dipolar couplings of weakly aligned molecules were discovered to measure the orientation of bond vectors relative to the alignment tensor (see Sect 16.5). Measurement of cross-correlated relaxation was described experimentally earlier for homonuclear cases [40, 41] and is widely used in solid-state NMR [42 14]. 

In solution, dipole-dipole interactions constitute a relaxation mechanism, and the dipolar relaxation which is the basis for the well-known nuclear Overhauser effect (NOE), mostly used in the homonuclear H, H case. The 2D HOESY method between H and Li has been used to obtain structural information of many organolithium systems in solution and this field was reviewed in 1995. Li is commonly used as the relaxation is dominated by the dipole-dipole mechanism and the relaxation time is relatively long. Knowledge of the proximity of the lithium cation relative to protons in the substrate is used to derive information about the structure and aggregation of organolithium systems in solution. In a few cases quantitative investigations have been made °. An average error of the lithium position of ca 0.2 A was reported. 

Chemical shift correlated NMR experiments are the most valuable amongst the variety of high resolution NMR techniques designed to date. In the family of homonuclear techniques, four basic experiments are applied routinely to the structure elucidation of molecules of all sizes. The first two, COSY [1, 2] and TOCSY [3, 4], provide through bond connectivity information based on the coherent (J-couplings) transfer of polarization between spins. The other two, NOESY [5] and ROESY [6] reveal proximity of spins in space by making use of the incoherent polarization transfer (nuclear Overhauser effect, NOE). These two different polarization transfer mechanisms can be looked at as two complementary vehicles which allow us to move from one proton atom of a molecule to another proton atom this is the essence of a structure determination by the H NMR spectroscopy. 

All of the protons in each of 12 thermo- and photochromic BIPS were assigned through a combination of homonuclear decoupling experiments and correlation spectroscopy. The relative stereochemistry of the gem-dimethyl groups could be assigned on the basis of Nuclear Overhauser Effect (NOE) experiments.131... 

Mismatch-optimized IS transfer Nuclear Overhauser enhancement Nuclear Overhauser effect spectroscopy Numerically optimized isotropic-mbdng sequence Preservation of equivalent pathways Pure in-phase correlation spectroscopy Planar doubly selective homonuclear TACSY Relayed correlation spectroscopy Radiofrequency... 

Abbreviations NMR, nuclear magnetic resonance 2D-NMR, two-dimensional NMR HOHAHA, 2D-NMR homonuclear Hartman-Hahn spectroscopy NOE, nuclear Overhauser effect NOESY, 2D-NMR nuclear Overhauser effect spectroscopy rf, radio frequency FID, free induction decay CD, circular dichroism PF4, platelet factor-4 IL-8, interleukin-8 Gro-a, growth-related protein a. 

The nuclear Overhauser effect provides information on the spatial proximity of nuclei (Section 5-4). NOE determinations are usually homonuclear, in the case of protons, but also can be heteronuclear, with signals irradiated and those of heteronuclei observed. NOE s occupy both an intermediary and a final position in the overall progression of structural determination. In most cases, NOE s afford information on the three-dimensional structure of a molecule after its two-dimensional structure has been determined. NOE s, however, also can be used earlier in the structural elucidation process, to provide answers to questions concerning stereochemistry in systems containing double bonds or rings. 

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. 

Traditionally, homonuclear 2D double quantum filtered correlation spectroscopy (DQF-COSY) and total correlated spectroscopy (TOCSY) spectra are valuable in the identification of resonances of individual monosaccharide units. In the presence of small couplings, through space connectivities detected by NOESY/ROESY (nuclear Overhauser effect spectroscopy/ rotational nuclear Overhauser effect spectroscopy) experiments are also useful in completing the resonance assignment. When the H NMR spectra of complex oligosaccharides are too crowded to fully elucidate the structure by homonuclear correlation methods, it is efficient to use 2D heteronuclear correlation methods, such as heteronuclear single quantum correlation... 

The methyl resonances of several oleanene derivatives have been assigned using lanthanide shifts and homonuclear INDOR techniques to measure the nuclear Overhauser effects between methyl signals. The assignments of the resonances of a series of 18jSH- and 18aH-oleanenes have been published. The potential use of molecular rotation differences in the identification of triterpenoid structures has been discussed. ... 

NMR is the tool most widely used to identify the structure of triterpenes. Different one-dimension and two-dimension techniques are usually used to study the structures of new compounds. Correlation via H-H coupling with square symmetry ( H- H COSY), homonuclear Hartmann-Hahn spectroscopy (HOHAHA), heteronuclear multiple quantum coherence (HMQC), heteronuclear multiple bond correlation (HMBC), distortionless enhancement by polarisation transfer (DEPT), incredible natural abundance double quantum transfer experiment (INADEQUATE) and nuclear Overhauser effect spectroscopy (NOESY) allow us to examine the proton and carbon chemical shift, carbon types, coupling constants, carbon-carbon and proton-carbon connectivities, and establish the relative stereochemistry of the chiral centres. 

The nuclear Overhauser effect (NOE), caused by dipole-dipole crossrelaxation, has great potential in the elucidation of the molecular structure and conformation (Noggle and Shirmer, 1971 Hall and Sanders, 1980). A homonuclear NOE can theoretically be as large as 50%, but is usually much smaller, and depends on the inverse sixth power of the distance between the nuclei, so that the relative magnitudes of enhancements reflect the spatial relationships of the atoms involved. 

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