## Abstract The ^77^Se chemical shifts of 79 mono‐ or disubstituted benzo[__b__]selenophenes are reported. The results in the 2‐ and 3‐substituted derivatives closely parallel those previously obtained in the corresponding selenophenes. The measured parameters also correlate well with those measure
Selenium-77 magnetic resonance in SSe and SeSe isosteres of phenanthrene
✍ Scribed by Marcel Baiwir; Gabriel Llabrès; Jean-Louis Piette; LÉOn Christiaens
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 263 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Selenium‐77 magnetic resonance spectra of sulphur‐selenium and selenium‐selenium isosteres of phenanthrene and some of their 2‐substituted derivatives have been recorded and 48 ^77^Se chemical shifts are presented. The two isomers of the studied compounds could be differentiated because the Se nucleus is always more shielded in the ‘trans’ than in the ‘cis’ isomer, the difference varying between 10 and 40 ppm. CNDO calculations have been performed; they allow an electronic model to be proposed which accounts, at least qualitatively, for the NMR results. They also provide an electronic interpretation of the ring opening of the Se‐containing ‘cis’ isomers when treated with alkyllithium.
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## Abstract ^77^Se was measured by inverse proton detection using multiple‐quantum ^1^H‐{^77^Se} correlation spectroscopy. One‐and two‐dimensional heteronuclear multiple quantum coherence (HMQC) experiments are reported for selenophene, benzeneselenol, dimethyl selenide, dimethyl diselenide, and D,
## Abstract The ^1^H, ^13^C and ^77^Se chemical shifts have been measured for mononitrobenzo[**__b__**]selenophenes. For the homocyclic nuclei, the observed ^1^H‐ and ^13^C‐values calculated from the empirical increments of nitrobenzene. Anomalous effects are observed in the 2‐ and 3‐substituted de