## Abstract The carbon‐13 chemical shifts of strychnine and ten closely related analogues have been assigned and confirmed in several cases using selective proton decoupling techniques. Where additivity relationships are used the importance of having data on an array of structural analogues is emph
Carbon-13 n.m.r. characterization of indenyllithium in solution
✍ Scribed by Ulf Edlund
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 286 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C N.m.r. chemical shifts obtained for indenyl‐ and cyclopentadienyllithium in several, mostly ethereal, solvents are presented. The chemical shift changes induced by varying the solvent are assumed to probe the actual π‐electron density distribution, thus providing an insight into the structure of the ion‐pair. The increase in the estimated π‐electron densities obtained for the protonated aromatic carbons of indenyllithium by increasing the coordinating ability of the solvent gives evidence of a change of the ion‐pair equilibrium towards solvent‐separated species. The average chemical shifts for indenyl‐ and cyclopentadienyllithium were independent of the choice of solvent, a fact which supports the ion‐pair model in all studied media.
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