## Abstract The ^13^C, ^15^N and ^77^Se NMR data (chemical shifts and coupling constants) of some cycloakenoโ1,2,3โselenadiazoles are presented. Extremely large ^77^Se chemical shifts are found. ^15^N, ^77^Se coupling constants, obtained at natural abundance, are reported for the first time. Strong
77Se and 13C NMR spectroscopy of some 1,2,3-selenadiazoles
โ Scribed by Helmut Duddeck; Torsten Hotopp
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 264 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
Abstract
^77^Se and ^13^C chemical shift of 19 1,2,3โselenadiazoles are discussed in terms of substituent effects and conformaโtional behaviour of the molecules. It is shown that the ^77^Se chemical shifts of such compounds are suitable tools for chiral discrimination in diastereomeric compounds.
๐ SIMILAR VOLUMES
## Abstract The results of ^13^C and (when pertinent) ^77^Se NMR spectra of thiopene and selenophene derivatives containing exocyclic selenium atoms are presented. The ^77^Se spectra show an interaction between nitro or carbonyl groups and selenium when they are __ortho__ to each other. The measure
C and 77Se NMR was carried out on dicyclopentadienyl derivatives of Ti, Zr and W with selenium bonded directly to the metal. Although '"C NMR is not sensitive to different substitution, 77Se NMR is valuable and refiects the influence of the different organic substituents and the nature of the metals
1-Aryl-4-carboxy-5-methyl-1,2,3-triazoles were prepared by the condensation of aryl azides with ethyl acetoacetate. The structures of these compounds were characterized by MS, IR and 1H and 13C NMR spectroscopy. The measured and calculated 13C chemical shifts of the aromatic carbons were compared.
Numerous areneselenenamides derived from ammonia, primary and secondary amines and two N,N-bis(ary1-se1eno)alkylamines have been studied. The selenenamides bearing an electron-withdrawing substituent on the aromatic moiety are stable. The 'H, 13C and 77Se chemical shifts and some coupling constants
The uC NMR spectra of three mesoionic 1,2,3-triazol-4-ylacetamides and two 1,2,3-triazol-4-ones were determined, and an evaluation of the shifts in relation to their mesoionic structure was made. A h e a r correlation between the I3C resonances and net charge densities, calculated by the CNDO/% meth