## Abstract Carbon‐13 chemical shifts and ^13^C−^15^N coupling constants of substituted benzaldoximes and of two non‐aromatic oximes have been determined. The coupling constants display little variation as a function of the nature or position of substitution, which suggests that perturbations in th
Carbon-13carbon-13 coupling constants of 13C-methyl labeled o- and p-substituted toluenes
✍ Scribed by James L. Marshall; Arthur M. Ihrig
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 300 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
From ^13^C‐7 labeled toluene the following ^13^C‐methyl o‐ and p‐substituted toluenes were synthesized: o‐NO~2~, ‐NH~2~, ‐I and CN; p‐NO~2~ and ‐NH~2~. Each of these labeled compounds was studied by carbon magnetic resonance to determine all carbon‐13carbon‐13 splittings involving the methyl carbon.
📜 SIMILAR VOLUMES
## Abstract The application of selective population inversion (SPI) to the assignment of ^13^C resonances and to the determination of the relative sign of ^13^C^1^H coupling constants is demonstrated for 1‐phenyl‐1,2‐dibromo‐2‐nitroethane. A negative sign for the geminal C‐2H‐1 coupling constant
## Abstract The carbon‐13 chemical shifts and coupling constants (__J__[^13^C^199^Hg]) have been determined for a series of eleven symmetrically substituted organomercurials. Empirical substituent parameters can be calculated which correlate observed and predicted chemical shifts for dialkylmercur
## Abstract The ^31^P^31^P and ^13^C^31^P coupling constants in 1,6‐diphosphatriptycene have been obtained from analysis of its proton decoupled ^13^C n.m.r. spectra. More accurate data, however, resulted from simultaneous analysis of the proton decoupled ^13^C spectra and ^31^P(^13^C) satellite
## Carbon -13 chemical shifts and J(PC) coupling constants of 29 vinyl phosphate derivatives are presented. In the series of compounds (RIO)zP(0)OC'(R~)=CzX, (where 3 R: indicates the first carbon of the Rz substituent) large differences were found between the 3J(P, 0, C-1, C-3) and 3J(P, 0, C-1,