## Abstract A series of substituted tetraselenafulvalenes (TSeFs) was studied in solution using ^1^H, ^13^C and ^77^Se NMR spectroscopy. Chemical shifts and heteronuclear coupling constant values were determined and assigned. Novel two‐dimensional H(Se)C and H(C)Se triple‐resonance correlation expe
77Se, 13C and 1H NMR investigations on ortho-carbonyl benzeneselenenyl derivatives
✍ Scribed by Gabriel Llabrès; Marcel Baiwir; Jean-Louis Piette; Léon Christiaens
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 287 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
o‐Carbonyl benzeneselenenyl compounds with COCH~3~, CHO and COOCH~3~ as carbonyl functions and SeCl, SeBr, SeSCN, SeSeCN, SeCN and SeCH~3~ as selenium‐containing groups, have been studied by ^1^H, ^13^C and ^77^Se NMR spectroscopy. The IR CO stretching frequencies of these compounds are also reported. If the SeCH~3~ derivatives are excluded, the compounds mainly adopt a planar ‘cis’ conformation, due to an interaction between the CO group and the selenium atom. The range of over 800 ppm for the observed ^77^Se chemical shifts makes ^77^Se NMR spectroscopy a powerful tool for physical organic chemists.
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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
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