Achieving an unprecedented degree of universality, the valence state potential energy curve (VS−PEC) reproduces the inner branch of 50 “experimental” RKR−PECs to an accuracy of 1.14% average unsigned deviation. The scaled RKR curves of 50 molecules with calculated partial charges, 0 ≤ δ < 0.9, coalesce into virtually a single curve in the Coulson−Fischer range, 0.5 R e ≤ R ≤ 1.5 R e, when plotted against q VS = z 1/2 ( R − R e )/ R e, with z = α e ν̃ e /2 B e 2 . The ground-state dissociation energy D e can be predicted from the equilibrium spectroscopic constants B e, ν̃ e, α e and the calculated VS promotion energy.
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Gardner et al. (1999) studied this question.
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