7 4^ \circ \) with respect to the static magnetic field B 0 (Andrew et al. 1958; Lowe 1959) yielding (3cos2 θ − 1 = 0). When the sample is spun at the magic angle, the anisotropic part produces NMR

sidebands and with fast rotation, the sidebands are shifted away, and the spectrum consists of narrow lines at the isotropic shifts. Only the term σisoγB 0 in Eq. 4 remains, and high resolution spectra GDC-0994 datasheet are obtained in solid state. In practice, the dipolar Topoisomerase inhibitor interactions \( \textH_\textD^II \) are not averaged for an abundant proton system where the chemical shift dispersion is small as compared to the dipolar interactions. Fig. 1 Schematic representation of the MAS technique. The spinning axis of the sample is at an angle of 54.74º (magic angle) with respect to the static magnetic field B0 Cross polarization The elemental composition of organic and biomolecules is primarily hydrogen, carbon, nitrogen, and oxygen, of which the first three elements are spin 1/2. Proton spins having a large natural abundance also have a high gyromagnetic ratio γ, which are the two main factors that determine the sensitivity of an NMR experiment. PU-H71 solubility dmso Hence, protons have the highest sensitivity of all the naturally occurring spins. However, the homonuclear dipolar couplings between 1H spins are considerable. In addition,

the topology of protons in molecules is such that they form

a dense network of strongly coupled spins, with effective overall couplings of ~50 kHz. These dipolar interactions induce severe line broadening in solids. Even with MAS, high resolution 1H NMR spectroscopy is still difficult in solids. Low abundance, e.g., for 13C and 15N, on the other hand, inevitably results in less-sensitive NMR spectra, and less signal-to-noise (S/N) ratio. In addition, the relaxation times of dilute nuclei are rather long, due to the absence of homonuclear dipolar interactions that induce relaxation transitions. In solid-state NMR, isotope labeling is often used when enhanced sensitivity is required. It is possible to further enhance the peak resolution and signal intensity in the MAS experiment by the transfer of the 1H transverse magnetization acetylcholine to a dilute spin species via CP in combination with high power proton decoupling (Bennett et al. 1995; Hartmann and Hahn 1962; Pines et al. 1973; Schaefer and Stejskal 1976). The separation between the spin up and spin down energy levels for 1H exceeds the splitting for 13C, for example, given by \( \gamma_{{{}^ 1\textH}} /\gamma_{{{}^ 1 3\textC}} \approx 4 \). The 1H polarization in the magnetic field B 0 is, therefore, larger than the 13C polarization. In the magnetic field B 0, it is not possible to transfer longitudinal magnetization from 1H to 13C (Fig. 2a). If an rf field B 1 is applied (Fig.