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A wide range of NMR spectra can be acquired including 1D, 1D with decoupling, solvent suppression, DEPT, T1, T2 and 2D HETCOR, HMBC, HMQC, COSY and JRES spectra. Pulsed field gradients for spectroscopy are included, and optional Diffusion pulsed field gradients [22] can also be added.
Recent advances in this technique include the 1D-CSSF (chemical shift selective filter) TOCSY experiment, which produces higher quality spectra and allows coupling constants to be reliably extracted and used to help determine stereochemistry. TOCSY is sometimes called "homonuclear Hartmann–Hahn spectroscopy" (HOHAHA). [12]
A 900 MHz NMR instrument with a 21.1 T magnet at HWB-NMR, Birmingham, UK Nuclear magnetic resonance spectroscopy, most commonly known as NMR spectroscopy or magnetic resonance spectroscopy (MRS), is a spectroscopic technique based on re-orientation of atomic nuclei with non-zero nuclear spins in an external magnetic field.
Nuclear Overhauser Effect Spectroscopy (NOESY) is a 2D NMR spectroscopic method used to identify nuclear spins undergoing cross-relaxation and to measure their cross-relaxation rates. Since 1 H dipole-dipole couplings provide the primary means of cross-relaxation for organic molecules in solution, spins undergoing cross-relaxation are those ...
Proton nuclear magnetic resonance (proton NMR, hydrogen-1 NMR, or 1 H NMR) is the application of nuclear magnetic resonance in NMR spectroscopy with respect to hydrogen-1 nuclei within the molecules of a substance, in order to determine the structure of its molecules. [1]
Wavenumber, as used in spectroscopy and most chemistry fields, is defined as the number of wavelengths per unit distance, typically centimeters (cm −1): ~ =, where λ is the wavelength.
The heteronuclear single quantum coherence or heteronuclear single quantum correlation experiment, normally abbreviated as HSQC, is used frequently in NMR spectroscopy of organic molecules and is of particular significance in the field of protein NMR. The experiment was first described by Geoffrey Bodenhausen and D. J. Ruben in 1980. [1]
13 C NMR spectroscopy is much less sensitive (ca. by 4 orders of magnitude) to carbon than 1 H NMR spectroscopy is to hydrogen, because of the lower abundance (1.1%) of 13 C compared to 1 H (>99%), and because of a lower(0.702 vs. 2.8) nuclear magnetic moment.