The conformational analysis of aromatic methoxyl groups from carbon-13 chemical shifts and spin-lattice relaxation times
✍ Scribed by Alexandros Makriyannis; James J Knittel
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 233 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
In a series of polymethoxy benzaldehydes and acetophenones it was found that diorthosubstitution distorts the Ar-OCH3 conformation. This distortion is accompanied by a downfield shift in the corresponding methoxyl 13C frequencies and an increase in their spin-lattice relaxation times.
📜 SIMILAR VOLUMES
## Abstract Carbon‐13 NMR relaxation data obtained for methyl groups in two dicyclohexane compounds were used to compare the Woessner and ‘model‐free’ approaches. It is shown that the extra flexibility offered by the latter leads to a more successful analysis of the data.
High-resolution 13C NMR spectra of 15 samples of uncomplexed and metalcomplexed tetranactin and nonactin were recorded in the solid state, revealing characteristic displacements of peaks due to complex formation and the effect of crystalline packing on the 13C chemical shifts and spidattice relaxati