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Analysis of 13C, 14N residual dipolar coupling in the 13C CP/MAS NMR spectra of ribonucleosides

✍ Scribed by Alejandro C. Olivieri; Lucio Frydman; Mariano Grasselli; Luis E. Diaz


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
530 KB
Volume
26
Category
Article
ISSN
0749-1581

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✦ Synopsis


956, Buenos Aires (1 113), Argentina I3C CP/MAS NMR spectra of nitrogen-containing compounds often show complex signals when recorded at low field strengths. This effect is due to the 13C, '"N residual dipolar coupling which is not averaged to zero by magic-angle spinning. Solidstate 13C NMR spectra at 25 MHz of ribonucleosides are analysed on the basis of the isotropic chemical shifts measured at 50 MHz, together with the asymmetric splittings caused by the presence of 14N calculated using a first-order equation. X-ray diffraction and NQR data, together with several assumptions regarding the quadrupole tensor at each '"N site, are used to obtain a successful spectral simulation.


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