Organic Magnetic Resonance · 1981 · 79 citations · 19 references
Natural SciencesChemistryOrganic ChemistrySpectroscopic AnalysisSpectroscopyHeterocyclic ChemistryMolecular SpectroscopyStructural ElucidationPhosphorus-31 Nuclear Magnetic Resonance
Abstract The olefins Ph 2 P(X)CHCHR [X=lone pair, O, S, Ch 3 I ; RCh 3 , ph, P(X)ph 2 ] have been prepared and their 1 H, 13 C and 31 P NMR spectra measured. trans 3 J [P(IV)C] (range 18.3–25.7 Hz) is greater than cis 3 J [P(IV)C] (range 6.9–11 Hz) but this relationship does not hold for P(III) compounds. In the 31 P spectra the E isomer absorbs to higher field than the Z isomer for P(III) and P(IV) compounds. The 1 H data are in accord with previous results; average substituent shielding coefficients for ph 2 P(X) substituted alkenes are reported.
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Annual Reports on N M R Spectroscopy
W.B. Jennings · Analytica Chimica Acta · 1974 · 77 citations
Natural Sciences, Chemistry, Physics +12
Louis D. Quin, Michael J. Gallagher, Glen T. Cunkle et al. · Journal of the American Chemical Society · 1980 · 76 citations