Hyperconjugation in .beta.-substituted ethyl radicals. Does it

Christopher J. Easton and Martin C. Merrett ... A. Geeson , Christopher J. Rhodes , Martyn C. R. Symons , Stephen F. J. Cox , Christopher A. Scott , E...
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It is also interesting to point out that extrapolation to 4J~.4 values t of 2.8 and 3.5 Hz, respectively, which in view of the uncertainty of Z and Z ' values for the pure gg-g'g' state may be considered to be in good agreement with the Hal12-4 estimates for W coupling in phosphate esters and with Duval, et U Z . , ~ ~ , ' ' ~on acyclic esters. It it also note(-0.8 Hz) is predicted for worthy that a negative 4J~-4t a @-5'-nucleotide with P,, = 0 % . As yet no negative 4JpHcoupling has been reported in phosphate esters, l7 though on the basis of the conformational dependence of the sign of 4JHcccHin propanes1sa19a negative 4Jp.41 for a g/t @-5'-nucleotide may not be unexpected.20 Figures l a and b can be of some practical value since they may provide crude estimates of Z and 2' (as well as P,, and Pg!gt)from 4J~.4t and may be useful in those situations where the 5 ' 5 ' ' regions defy analysis. We stress caution in the application since additional splitting (broadening) in the 4' region can arise from virtual coupling. 2 1 However, we may safely predict that if 4Jp.4tis >1.0 Hz, the predominant conformer is small (