Proton NMR spectra are reported for chlorotrimethylstannane, tetramethylstannane, tetramethylplumbane and dimethylmercury containing various combinations of CH, and CD, groups. Additive long-range isotope effects on chemical shifts, 4AH(D), are observed to result in increased shielding of essentiall
Conformational and long-range low field steric deuterium isotope effects on carbon chemical shifts
✍ Scribed by T. Pehk; A. Laht; E. Lippmaa
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 252 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Comparison of the room and low temperature (203 K) ^13^C NMR spectra of 3‐cis‐bicyclo[4.4.0]decanone and its 2,2,4,4‐tetradeuterio isotopomer provides information about the deuterium isotope effect on the conformational equilibrium in this compound. Four‐bond low field deuterium isotope effects on some carbon chemical shifts are observed. These effects can be used for unambiguous assignment of the ^13^C lines to carbon atoms in alicyclic compounds.
📜 SIMILAR VOLUMES
## Abstract Long‐range deuterium isotope effects on ^13^C chemical shifts, ^__n__^ΔC(OD), were studied in the intramolecularly hydrogen‐bonded purpurogallins (benzotropolones). A very large long‐range isotope effect from the hydrogenbonded 4‐OH(D) is observed over six bonds at C‐7. Further, long‐ra