Abstract
N.m.r, data for fifteen 1,4-benzoquinones,
four 1,4-naphthoquinones, and six cyclohex-2-ene-1,4-diones are tabulated. From
these, and previously available data, it is possible to obtain characteristic
ranges for methyl-allylic coupling constants (c 1.3 c/s) and methyl-methyl
homoallylic coupling constants (c. 1.3 c/s) for this for this series of
compounds as well as values for other long-range and vicinal interactions,
including a negative coupling across five bonds. On
the basis of both chemical shifts and coupling constants it was concluded that
1,4-benzoquinones have little aromaticity from the N.M.R. point of view.
The halogen atoms in
5,6-dihalogenocyclohex-2-ene-1,4-diones appear to be tram diaxial.
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