## Abstract The ^1^H and ^13^C NMR spectra of some bis(benzocrown ethers) were recorded and assigned by means of ^1^H/^13^C HETCOR spectroscopy, heteronuclear selective decoupling experiments and the refocused INEPT experiment optimized for long‐range ^1^H, ^13^C coupling constants. It is shown tha
The stereochemistry of crown ethers. II —1H and 13C NMR structural study in solution
✍ Scribed by E. Kleinpeter; M. Gäbler; W. Schroth; J. Mattinen; K. Pihlaja
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 335 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 'H and I3C NMR spectra of a series of structurally related crown ethers have been recorded, and the signals assigned by means of 'H/I3C heteronuclear correlated and 'H/'H homonuclear NOE difference spectroscopy. The NMR parameters so extracted have been used to discuss the preferred, rapidly interconverting solution conformations of the studied species The high-field shifts in the I3C NMR spectra, within the so-called y-fragments, and also the 'H/'H homonuclear NOES, are particularly informative in this respect. The T, relaxation times of the I3C atoms show segmental motions within the ether segments and suggest different intramolecular flexibilities for the studied compounds.
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