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Overhauser effect spectroscopy

For large molecules, such as proteins, the main method in use is a 2D technique, called NOESY (nuclear Overhauser effect spectroscopy). The basic experiment [33, 34] consists of tluee 90° pulses. The first pulse converts die longitudinal magnetizations for all protons, present at equilibrium, into transverse magnetizations which evolve diirhig the subsequent evolution time In this way, the transverse magnetization components for different protons become labelled by their resonance frequencies. The second 90° pulse rotates the magnetizations to the -z-direction. [Pg.1510]

The 2-D nuclear Overhauser effect spectroscopy (2-D-NOESY) experiment resembles the COSY however, the cross-peaks arise from... [Pg.408]

NOESY Nuclear Overhauser effect spectroscopy, detection of NOE in the HH COSY square format, traces out closely spaced protons in larger molecules... [Pg.267]

Figure 1. Pulse sequences of some typical 2D-NMR experiments. COSY = correlation SpectroscopY, DQFCOSY = Double Quantum Filtered COSY, RELAY = RELAYed Magnetization Spectroscopy, and NOESY = Nuclear Overhauser Effect SpectroscopY. Figure 1. Pulse sequences of some typical 2D-NMR experiments. COSY = correlation SpectroscopY, DQFCOSY = Double Quantum Filtered COSY, RELAY = RELAYed Magnetization Spectroscopy, and NOESY = Nuclear Overhauser Effect SpectroscopY.
Rao, B. D. N. Two-dimensional transferred nuclear Overhauser effect spectroscopy (TRNOESY) smdies of nucleotide conformations in creatine kinase complexes effects due to weak nonspedftc binding. Biochemistry 1993,... [Pg.251]

Guichard, G., Briand, J. P., Muller, S., Cung, M. T. Structure of antibody-bound peptides and retro-inverso analogues. A transferred nuclear Overhauser effect spectroscopy and molecular dynamics approach. Biochemistry 2001, 40, 5720-5727. [Pg.251]

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). [Pg.123]

GOESY Gradient Overhauser effect spectroscopy. An early version of a 1-D NOESY making use of gradients. [Pg.207]

NOESY Nuclear Overhauser effect spectroscopy. Two-dimensional technique that correlates nuclei to each other if there is any NOE between them. [Pg.208]

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. [Pg.209]

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

Conformations of mycothiol bimane (MSmB) were studied by H and 13C NMR using rotational nuclear Overhauser effect spectroscopy (ROESY) and heteronuclear single quantum correlation (HSQC) methods with expansions of the anomeric region <2003JOC3380>. NMR characterization of iV-acetyl-L-(Y)-cysteinyl monobimane and peracetylated MSmB was also published (Section 12.10.15.4) <2002JA3492>. [Pg.374]

Benzoylation of D-g/ycero-D-gw/o-heptono-1,4-lactone with an excess of benzoyl chloride and pyridine afforded the hept-2-enono-1,4-lactone as the main product (198). The di- and triunsaturated compounds were isolated in very low yield from the mother liquors (199). Higher yields of the di- and triunsaturated derivatives 153 and 154 were obtained when the /5-elimination reaction was performed with triethylamine on the previously synthesized per-O-benzoyl D-g/ycero-D-gw/o-heptono-1,4-lactone. Employing 10% triethylamine in chloroform, the lactone 153 was obtained as an E, Z dias-tereomeric mixture in 9 11 ratio as determined by H n.m.r. When 20% triethylamine was used, the furanone 154 was obtained in 59% yield (200). Its structure was assigned, on the basis of H and 13C n.m.r. spectra, as 3 -benzoyloxy - (5Z)-[(Z)-3 - benzoyloxy - 2 - propenyliden] -2(5 H)- furanone. The stereochemistry of the exocyclic double bonds was established (201) by nuclear Overhauser effect spectroscopy (NOESY). [Pg.167]

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. [Pg.94]

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. [Pg.95]

With the aid of 13C NMR, 6Li NMR and XH HOESY (heteronuclear Overhauser effect spectroscopy) NMR of a-lithiomethoxyallene (106) and l-lithio-l-ethoxy-3-J-butylallene (107) as well as by ab initio model calculations on monomeric and dimeric a-lithiohy-droxyallene, Schleyer and coworkers64 proved that 106 and 107 are dimeric in THF (106 forms a tetramer in diethyl ether) with a nonclassical 1,3-bridged structure. The 13C NMR spectrum of allenyllithium in THF is also in agreement with the allenic-type structure the chemical shift of C2 (196.4 ppm) resembles that of neutral allene (212.6 ppm), rather than C2 of propyne (82.4 ppm). [Pg.167]

Another, yet completely different access to macroscopic binding strengths of selectands on CSPs has been described by Hellriegel et al. [65] employing suspended-state NMR spectroscopy. Thus, HR-MAS 2D transfer-nuclear Overhauser effect spectroscopy (NOESY) was utilized to distinguish solutes strongly binding to the... [Pg.47]

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. [Pg.49]

TTie TOCSY 2D NMR experiment correlates all protons of a spin system, not just those directly connected via three chemical bonds. For the protein example, the alpha proton, Ft , and all the other protons are able to transfer magnetization to the beta, gamma, delta, and epsilon protons if they are connected by a continuous chain—that is, the continuous chain of protons in the side chains of the individual amino acids making up the protein. The COSY and TOCSY experiments are used to build so-called spin systems—that is, a list of resonances of the chemical shift of the peptide main chain proton, the alpha proton(s), and all other protons from each aa side chain. Which chemical shifts correspond to which nuclei in the spin system is determined by the conventional correlation spectroscopy connectivities and the fact that different types of protons have characteristic chemical shifts. To connect the different spin systems in a sequential order, the nuclear Overhauser effect spectroscopy... [Pg.114]

Two-dimensional (2D) Nuclear Overhauser Effect Spectroscopy (NOESY) has been proven to be a valuable technique which provides both structural and... [Pg.172]


See other pages where Overhauser effect spectroscopy is mentioned: [Pg.1511]    [Pg.408]    [Pg.124]    [Pg.90]    [Pg.91]    [Pg.110]    [Pg.365]    [Pg.196]    [Pg.740]    [Pg.111]    [Pg.88]    [Pg.500]    [Pg.102]    [Pg.112]    [Pg.115]    [Pg.16]    [Pg.17]    [Pg.490]    [Pg.140]   


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Carbon-13, Overhauser effect spectroscopy

Correlated spectroscopy nuclear Overhauser effect

Gradient enhanced Overhauser effect spectroscopy

Heteronuclear Overhauser effect spectroscopy

NMR spectroscopy nuclear Overhauser effect

Nuclear Overhauser Effect (NOE) Difference Spectroscopy

Nuclear Overhauser effect difference spectroscopy

Nuclear Overhauser effect spectroscopy Fourier transform

Nuclear Overhauser effect spectroscopy association

Nuclear Overhauser effect spectroscopy combination experiments

Nuclear Overhauser effect spectroscopy coupling constant determination

Nuclear Overhauser effect spectroscopy resonance

Nuclear Overhauser effect spectroscopy spin assignment

Nuclear overhauser effect spectroscopy

Nuclear overhauser effect spectroscopy NOESY)

Nuclear overhauser effect spectroscopy structure determination

Overhauser

Overhauser effect spectroscopy HOESY

Overhauser effect spectroscopy NOESY

Overhauser effect spectroscopy ROESY

Overhauser spectroscopy

Rotating frame Overhauser effect spectroscopy

Rotating frame Overhauser effect spectroscopy (ROESY

Rotating frame nuclear Overhauser effect spectroscopy

Rotation-frame Overhauser Effect Spectroscopy

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