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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.


📜 SIMILAR VOLUMES


Carbon-13 spin-lattice relaxation times
✍ Geoffrey E. Hawkes; Raymond J. Abraham 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 English ⚖ 351 KB

## 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