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Orientations of the principal components of electric field gradients and internal motions in dihydrogen ligands from the 2H T1 NMR relaxation data in solution

✍ Scribed by Vladimir I. Bakhmutov


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
123 KB
Volume
42
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The deuterium spin–lattice relaxation times in (D~2~) ligands of W, Ru and Os complexes are reviewed and analyzed in terms of the fast internal (D~2~) motions: free rotation, librations and 180° jumps. The analysis was performed using quadrupolar coupling constant (DQCC) parameters taken from the solid‐state ^2^H NMR spectra and density function theory calculations. It is shown that the calculated DQCC values can be corrected for further use in interpretations of deuterium relaxation times for Ru and Os dihydrogen complexes. The resulting data led to a criterion for using the relaxation data to distinguish fast‐spinning dihydrogen ligands. It is shown that the principal components of electric field gradient tensors at D in the dihydrogen ligands are oriented closer to M–D directions Copyright © 2003 John Wiley & Sons, Ltd.