## Abstract Carbon‐13 spin‐lattice relaxation times (__T__~1~) and ^13^C‐{^19^F} nuclear Overhauser enhancement (NOE) factors have been measured for some simple fluorocarbons by pulse‐Fourier transform methods—‘progressive saturation’ and ‘dynamic Overhauser enhancement’. The NOE factors are shown
119Sn spin–lattice relaxation times and nuclear Overhauser enhancement factors in some organotin compounds
✍ Scribed by Stephen J. Blunden; Andrew Frangou; Duncan G. Gillies
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 436 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Dipole‐dipole relaxation via non‐bonded protons is an important relaxation mechanism for^119^Sn in tri‐n‐propyltin and tri‐n ‐butyltin compounds. This causes a negative nuclear Overhauser effect, arising from the negative magnetogyric ratio, which in some cases nulls the signal. The relative contributions from the spin‐rotation and dipole‐dipole mechanisms vary: larger molecules have lower spin‐rotation and higher dipolar relaxation rates. The practical significance of large nuclear Overhauser enhancement factors in recording ^119^Sn spectra and the relation of the dipole‐dipole contribution to the molecular motion and of the spin‐rotation contribution to the absolute shift scale for ^119^Sn are discussed.
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