Analysis of the NMR and Double-Resonance Spectra of the Isomers of N2F2
The assignment of F19 NMR spectra of the two isomers of N2F2 is consistent with the assumption of trans and cis 1,2-difluorodiazine structures for these molecules. The qualitative features of the F19—{N14} double-resonance spectra, and a comparison of the F19 NMR spectra at 56.4 and 40.0 Mc/sec stro...
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Veröffentlicht in: | The Journal of chemical physics 1962-07, Vol.37 (1), p.182-189 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The assignment of F19 NMR spectra of the two isomers of N2F2 is consistent with the assumption of trans and cis 1,2-difluorodiazine structures for these molecules. The qualitative features of the F19—{N14} double-resonance spectra, and a comparison of the F19 NMR spectra at 56.4 and 40.0 Mc/sec strongly favor a cis structure over a 1,1-difluorodiazine structure for the more reactive isomer. A comparison of the indirect N–F coupling constants for the two isomers indicates that the FNN angles are probably quite different for cis and trans N2F2. |
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ISSN: | 0021-9606 1089-7690 |
DOI: | 10.1063/1.1732949 |