The effect on the solid-state 'Li chemical shifts and quadrupolar coupling constants of different locations of the lithium cation relative to the carbanion framework of delocalized carbanions was investigated. When the lithium cation is situated above the conjugated system, the chemical shift is abo
7Li solid-state NMR spectroscopic study of cyclopentadienyllithium complexes
โ Scribed by Dan Johnels; Arne Boman; Ulf Edlund
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 230 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
Eighteen cyclopentadienyllithium complexes were studied by solid-state 7Li NMR spectroscopy. It is shown that the chemical shift gives information on the type of complex, i.e. whether the complex is a contact ion pair, a solvent-separated ion pair, a sandwich structure or a polymeric material. These shift di โ erences are due to the ring current of the aromatic anion. In order to obtain information about the solvation of the lithium cation, the quadrupolar coupling constant s has to be determined. The s value depends on the number and type of donor atoms in the ligand, where the nitrogen-containing ligands give rise to higher s values than the oxygen analogues.
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