## Abstract The small negative magnetogyric ratio (γ) of the ^15^N nucleus decreases the efficiency of ^15^N^1^H dipole‐dipole relaxation to about 25% of that for an analogous ^13^C nucleus. This may lead to greater competition from other relaxation mechanisms in ^15^N n.m.r. and consequent partia
Natural-abundance lithium-6 NMR spin–lattice relaxation in some simple organolithium compounds
✍ Scribed by F. W. Wehrli
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 258 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^6^Li, ^7^Li and ^13^C spin–lattice relaxation and NOE data are reported for methyllithium, butyllithium and phenyllithium with ^6^Li T~1~ values found in the order of tens of seconds and their relaxation 2–3 orders of magnitude less efficient than that for ^7^Li. The data indicate that ^6^Li is substantially relaxed by the intramolecular ^6^Li–^1^H mechanism, whereas both quadrupolar and ^6^Li–^7^Li dipolar relaxation are minor processes. The non‐linearity of the Arrhenius curve for Me^6^Li is compatible with a small spin–rotation contribution. Since ^6^Li in solution behaves essentially as a spin‐1/2 nucleus, it represents, in spite of its lower magnetic moment and overall sensitivity, an attractive alternative to ^7^Li NMR.
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