## Abstract The preferred conformations and the complexing behaviour of 16‐ and 17‐membered dibenzo crown ethers were studied by means of both NMR spectroscopy and molecular mechanical calculations. Conclusions could be drawn about the stoichiometry and stability of the alkali metal ion corand comp
Stereochemistry of crown ethers. I. Conformational and dynamic behaviour of N-tosyl-substituted diaza crown ethers
✍ Scribed by E. Kleinpeter; M. Gäbler; W. Schroth
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 405 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The variable-temperature 'H and 13C NMR spectra of some N-tosyl diaza crown ethers have been obtained. They are discussed with respect to the preferred conformers of the crowns and the free energies of activation of the interconversional process of the large ring. Both the preferred conformers and the ring interconversional barriers have been found to be strongly dependent on the structure and the ring size of the studied compounds. KEY WORDS Variable-temperature 'H and I3C NMR spectra N-tosyl diaza crown ethers Crown conformation Free energies of activation
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