## Abstract ^13^C FT n.m.r. spectra were obtained from borates of methyl α‐D‐glucopyranoside, triethylboron, sodium tetraphenylboron and 1‐butaneboronic acid employing a simultaneous ^1^H and ^11^B decoupling network. The effectiveness of the system was evident using the three latter organoboron co
N.m.r. studies on aromatic compounds. I—13C n.m.r. spectra of some mono- and disulpho-substituted hydroxycarboxylic acids
✍ Scribed by Kauko Räisänen; Lauri H. J. Lajunen
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 372 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Carbon‐13 n.m.r. spectra of 3‐hydroxy‐4‐sulpho‐2‐naphthoic, 3‐hydroxy‐5‐sulpho‐2‐naphthoic, 3‐hydroxy‐7‐sulpho‐2‐naphthoic, 5‐sulphosalicylic, 3‐hydroxy‐5,7‐disulpho‐2‐naphthoic, 1‐hydroxy‐4,7‐disulpho‐2‐naphthoic, and 3,5‐disulphosalicylic acids were recorded with and without proton noise‐decoupling. Analyses of the spectra were carried out for all compounds except 3‐hydroxy‐5‐sulpho‐2‐naphthoic acid which dimerized. The fine splitting caused by long‐range coupling was used in identifying the lines of the ^13^C n.m.r. spectra.
📜 SIMILAR VOLUMES
## Abstract The ^13^C n.m.r. spectra of complexes between __o__‐chloranil and aromatic electron donors were studied. Complexation leads to a general diamagnetic shift of the ^13^C n.m.r. signals for the acceptor (__o__‐chloranil), but for signals from the ^13^C nuclei in the donors both diamagnetic