Pronounced stereospecificity of (1)H, (13)C, (15)N and (77)Se shielding constants in the selenophenyl oximes as shown by NMR spectroscopy and GIAO calculations
In the (1)H and (13)C NMR spectra of 1-(2-selenophenyl)-1-alkanone oximes, the (1)H, the (13)C-3 and (13)C-5 signals of the selenophene ring are shifted by 0.1-0.4, 2.5-3.0 and 5.5-6.0 ppm, respectively, to higher frequencies, whereas those of the (13)C-1, (13)C-2 and (13)C-4 carbons are shifted by...
Publié dans: | Magnetic resonance in chemistry : MRC. - 1985. - 47(2009), 10 vom: 01. Okt., Seite 879-84 |
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Auteur principal: | |
Autres auteurs: | , , , |
Format: | Article en ligne |
Langue: | English |
Publié: |
2009
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Accès à la collection: | Magnetic resonance in chemistry : MRC |
Sujets: | Journal Article Carbon Isotopes Nitrogen Isotopes Organoselenium Compounds Oximes Protons Selenium H6241UJ22B |
Résumé: | In the (1)H and (13)C NMR spectra of 1-(2-selenophenyl)-1-alkanone oximes, the (1)H, the (13)C-3 and (13)C-5 signals of the selenophene ring are shifted by 0.1-0.4, 2.5-3.0 and 5.5-6.0 ppm, respectively, to higher frequencies, whereas those of the (13)C-1, (13)C-2 and (13)C-4 carbons are shifted by 4-5, approximately 11 and approximately 1.7 ppm to lower frequencies on going from the E to Z isomer. The (15)N chemical shift of the oximic nitrogen is larger by 13-16 ppm in the E isomer relative to the Z isomer. An extraordinarily large difference (above 90 ppm) between the (77)Se resonance positions is revealed in the studied oxime isomers, the (77)Se peak being shifted to higher frequencies in the Z isomer. The trends in the changes of the measured chemical shifts are well reproduced by the GIAO calculations of the (1)H, (13)C, (15)N and (77)Se shielding constants in the energy-favorable conformation with the syn orientation of the-C=N-O-H group relative to the selenophene ring |
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Description: | Date Completed 26.01.2010 Date Revised 21.11.2013 published: Print Citation Status MEDLINE |
ISSN: | 1097-458X |
DOI: | 10.1002/mrc.2471 |