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
Hauptverfasser: Noggle, Joseph H., Baldeschwieler, John D., Colburn, Charles B.
Format: Artikel
Sprache:eng
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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.
ISSN:0021-9606
1089-7690
DOI:10.1063/1.1732949