Cross homonuclear

A more useful type of 2D NMR spectroscopy is shift-correlated spectroscopy (COSY), in which both axes describe the chemical shifts of the coupled nuclei, and the cross-peaks obtained tell us which nuclei are coupled to which other nuclei. The coupled nuclei may be of the same type—e.g., protons coupled to protons, as in homonuclear 2D shift-correlated experiments—or of different types—e.g., protons coupled to C nuclei, as in heteronuclear 2D shift-correlated spectroscopy. Thus, in contrast to /-resolved spectroscopy, in which the nuclei were being modulated (i.e., undergoing... 

The ROESY spectrum affords homonuclear transverse nOe interactions as cross-peaks between the various dipolarly coupled hydrogens. This... 

Figure 17. Contour plot of the 360MHz homonuclear spin correlation mpa of 10 (2 mg, CDCL, high-field expansion) with no delay inserted in the pulse sequence shown at the top of the figure. Assignments of cross peaks indicating coupled spins in the E-ring are shown with tljie dotted lines. The corresponding region of the one-dimensional H NMR spectra is provided on the abscissa. The 2-D correlation map is composed of 128 x 512 data point spectra, each composed of 16 transients. A 4-s delay was allowed between each pulse sequence (T ) and t was incremented by 554s. Data was acquired with quadrature phase detection in both dimensions, zero filled in the t dimension, and the final 256 x 256 data was symmetrized. Total time of the experiment was 2.31 h (17).

Dipolar recoupling may also be accomplished using continuous rf irradiation as demonstrated in the heteronuclear and homonuclear case by the CP at MAS conditions (or for low-y heteronuclear spins called double-cross-polarization, DCP [103]) and HORROR (homonuclear rotary resonance) [26] experiments, respectively. These experiments may easily be described by transforming the description into the interaction frame of the rf irradiation using (14a) exploiting... 

Recently a new type of proton assisted recoupling experiments has been developed for coherence transfer where rf irradiation is taking place on all involved rf channels. This embraces the homonuclear proton assisted recoupling (PAR) [45, 140, 141] and the later resonant second-order transfer (RESORT) [142] experiments, as well as the heteronuclear proton assisted insensitive nuclei (PAIN) cross polarization [44] experiments. In PAR and PAIN, spin-lock CW irradiation is applied on both passive ( H) and active spins (13C, 15N) without matching rotary resonance conditions. In RESORT a phase alternation irradiation scheme for the passive spins is used. 

Fig. 10.22. Diagram showing the cross-polarization from protons, H, to a heteronucleus, X, such as carbons. Heteronuclear dipolar coupling enables the transfer of magnetization from H to X, such as protons to carbons. Homonuclear dipolar coupling between the abundant protons enables the redistribution of proton spin energy through spin diffusion.

Requirement 2. Self-consistency The peak lists must be faithful representations of the NOESY spectra, and the chemical shift positions of the NOESY cross peaks must be correctly calibrated to fit the chemical shift lists within the chemical shift tolerances. The range of allowed chemical shift variations ( tolerances ) for 1H should not exceed 0.02 ppm when working with homonuclear [1H,1H]-NOESY spectra, or 0.03 ppm when work-... 

Availability of a sample isotopically enriched with 15N and 13C offers the NMR spectro-scopist additional tools for overcoming the problems encountered in homonuclear experiments. In an obvious extension of the homonuclear experiments, the carbon or nitrogen dimension can be used to improve the resolution in NOESY spectra. However, recent trends clearly favor the through-bond approach where the presence of a cross peak unambiguously proves the existence of a chemical bond between the nuclei involved. Let us review briefly the experiments available for labeled oligonucleotides. 

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]. 

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