Abstract
Polarization-inversion (PI) has been applied to proton magic angle spinning (MAS) NMR spectra recorded under fast MAS conditions. The combination of cross-polarization (CP) from carbon to proton and subsequent polarization-inversion produces strong oscillatory behavior in the proton signal intensities at high MAS speeds of 60 kHz. It is observed that by a suitable choice of the polarization-inversion time, a proton spectrum free of methylene and methine protons can be obtained. Such a spectrum, on the one hand, increases the resolution of the crowded proton spectrum and on the other hand provides exclusively chemical shifts of protons such as NH, OH and SH which might otherwise overlap with carbon attached protons. The oscillations observed during PI can also be used to estimate the dipolar coupling between proton and carbon by Fourier transformation of data acquired at equally incremented time periods. The utility of the above ideas has been demonstrated on a set of molecules with both 13C labeled and 13C in natural abundance.
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