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A Universal Two-Parameter Kratzer-Potential and Its Superiority over Morse's for Calculating and Scaling First-Order Spectroscopic Constants of 300 Diatomic Bonds

✍ Scribed by Guido Van Hooydonk


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
732 KB
Volume
1999
Category
Article
ISSN
1434-1948

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✦ Synopsis


After decades of intensive research, the question remains relations between the constants. We show that ionic potentials of generalized Kratzer-type (Varshni's V th whether or not a universal two-or three-parameter potential exists. For a large number of about 300 bonds, we now potential) and their ionic Coulomb-like asymptotes Ae 2 /R e (with A close to 1) behave as simple universal two-parameter critically review the constraints for potentials and asymptotes, involved in three available scaling processes potentials. For both α e and ω e x e , this potential gives percentage deviations 2 to 3 times smaller than Morse's three (Varshni, Calder-Ruedenberg, and Graves-Parr). We show that the covalent Sutherland parameter can never be a parameter potential for hundreds of bonds. We also prove that the Graves-Parr scaling hypothesis is valid, despite universal scaling factor. This implies that the usual constraint U(R) = -D e at R = ϱ for potentials is only desirable and that these authors' own conclusion. We discuss various new relations between spectroscopic constants. the natural asymptote D e is not even needed to explain the troscopic constants of a large number of diatomic bonds low-parameter reduced potentials: a reputed covalent one Rozier 9, B-9000 Ghent, Belgium


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