## Abstract ^13^C NMR chemical shifts of a series of 2′,3′,4′‐trimethoxylated flavones are reported. The ^13^C NMR chemical shifts of 2′,3′, 4′‐trimethoxyflavone was reinvestigated by 2D NMR. It is shown that two signals which were assigned by the lanthanide shift reagent method in an earlier study
13C and 19F NMR spectra of a series of laterally fluorinated mesogens
✍ Scribed by Christa Loubser
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 239 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C and ^19^F NMR spectra of a series of mesogenic compounds, (S)‐4‐n‐octyloxy‐fluorobiphenyl‐4′‐yl fluoro‐4‐(2‐fluoro‐octanoyloxy)benzoates, were determined in solution. The effect of fluoro substitution in various positions on the ^13^C and ^19^F chemical shifts was studied. ^13^C, ^19^F and ^19^F, ^19^F scalar coupling constants are given.
📜 SIMILAR VOLUMES
The complete assignment of the 1H, 13C and 19F NMR spectra of eight Ñuoro-substituted 3H-naphthopyrans was achieved by the concerted application of homonuclear (1HÈ1H) and heteronuclear (13CÈ1H and 19FÈ1H) correlations.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract Liquid perfluorocarbons exhibit unique physical–chemical characteristics such as extraordinary stability, combined hydrophobia and lipophobia, low surface tension and a capacity to carry large quantities of gas. They have found widespread use in industry, medicine and biology even thoug
## Abstract The ^1^H, ^13^C, ^15^N and ^19^F NMR spectra of nine DL‐phenylalcoholamides bearing fluorine and chlorine as substituents of the phenyl ring are reported. All of them are active as anticonvulsants in pentylenetetrazole‐induced seizures. Copyright © 2003 John Wiley & Sons, Ltd.
The positions of the chemical shifts in the table match those of the carbon atoms at the head of a column. Assignments with similar chemical shifts may be interchanged. Fourth signal not resolved. Signals superimposed.