1976
DOI: 10.1016/s0066-4103(08)60426-3
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Fluorine-19 NMR Spectroscopy

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Cited by 17 publications
(8 citation statements)
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“…The spectral assignment for isoflurane has been well documented (Dubois and Evers, 1992; Mills et al, 1987; in Fig. 1 were based on theoretical consideration of throughbond shielding and through-space deshielding to the 19F nuclei by the Cl electron clouds (Cavalli, 1976;Feeney et al, 1966;Williamson and Braman, 1967) and were confirmed by the ratio of peak integration for the trans and cis forms of F6 and by 19F homonuclear decoupling spectroscopy. The same number of peaks, with a similar spectral pattern, was found for fully dissolved F3, F6, and F8 in water.…”
Section: Spectral Assignmentmentioning
confidence: 72%
“…The spectral assignment for isoflurane has been well documented (Dubois and Evers, 1992; Mills et al, 1987; in Fig. 1 were based on theoretical consideration of throughbond shielding and through-space deshielding to the 19F nuclei by the Cl electron clouds (Cavalli, 1976;Feeney et al, 1966;Williamson and Braman, 1967) and were confirmed by the ratio of peak integration for the trans and cis forms of F6 and by 19F homonuclear decoupling spectroscopy. The same number of peaks, with a similar spectral pattern, was found for fully dissolved F3, F6, and F8 in water.…”
Section: Spectral Assignmentmentioning
confidence: 72%
“…Direct, one-bond couplings are found to be negative in those molecules for which they have been determined. Accumulation of fluorines tends to decrease the magnitude of the coupling (entries 1-6), but accumulation of protons has even more effect (7)(8)(9)(10). Couplings to trigonal carbons (entries 11 and 12) are comparable to tetrahedral couplings, while those of aromatic carbons (entries 17-24) are somewhat reduced and show at most a weak dependence on the electronegativity of para substituents.…”
Section: F-13 C Couplingmentioning
confidence: 99%
“…1 ) Accumulation of halogen atoms on the same carbon also results in marked deshielding (entries [6][7][8][9]. Most of the generalizations that describe relative shielding in hydrocarbon groups 30 CF 3 CF 2 (2<) CF 2 (3() CF 2 (4) CF 2 (3) CF 2 (2) CF 3 F (4) 31 32 33 CF 3 CF 2 CF 2(2) CF 3 34 CF 2 -CF 2 35 Cvclo -C 6 have no applicability to fluorocarbon chains.…”
mentioning
confidence: 99%
See 1 more Smart Citation
“…A number of summaries of fluorine NMR spectroscopy have appeared (Mooney and Winson, 1968;Jones and Mooney, 1970;Fields, 1972Fields, , 1977Barlow, 1971, 1974;Phillips, 1974;Cavalli, 1976) as well as compilations of reported fluorine chemical shifts (Dungan and Van Wazur, 1970;Emsley and Phillips, 1971). A useful discussion of experimental considerations in executing Fourier transform FMR experiments with fluorinecontaining biological systems has also appeared (Sykes and Hull, 1978).…”
Section: Fluorine Magnetic Resonance Experimentsmentioning
confidence: 99%