Computations and 1 H NMR Spectroscopy of the Imide Region Can Distinguish Isomers of Hydrogen-Bonded Aggregates
✍ Scribed by Chin, Donovan N.; Simanek, Eric E.; Li, Xinhua; Wazeer, Mohammed I. M.; Whitesides, George M.
- Book ID
- 127290959
- Publisher
- American Chemical Society
- Year
- 1997
- Tongue
- English
- Weight
- 136 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The ^1^H, ^13^C and ^15^N NMR studies have shown that the __E__ and __Z__ isomers of pyrrole‐2‐carbaldehyde oxime adopt preferable conformation with the __syn__ orientation of the oxime group with respect to the pyrrole ring. The __syn__ conformation of __E__ and __Z__ isomers of pyrrol
## Abstract According to the ^1^H, ^13^C and ^15^N NMR spectroscopic data and DFT calculations, the __E__‐isomer of 1‐vinylpyrrole‐2‐carbaldehyde adopts preferable conformation with the __anti__‐orientation of the vinyl group relative to the carbaldehyde oxime group and with the __syn__‐arrangement