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Improved Spectroscopic Dissociation Energy for Ground‐State Ar2
1.Y. Tanaka and K. Yoshino, J. Chem. Phys. 53, 2012 (1970).
2.The highest observed level appeared in only one of the several series of bands, and its relative position (i.e., ) was not tabulated for this case.1 Hence, the present analysis uses only the data.
3.(a) R. J. Le Roy and R. B. Bernstein, J. Chem. Phys. 52, 3869 (1970);
3.(b) R. J. Le Roy and R. B. Bernstein, J. Mol. Spectry. 37, 109 (1971).
4.G. Starkschall and R. G. Gordon, J. Chem. Phys. 54, 663 (1971).
5.G. Starkschall and R. G. Gordon, J. Chem. Phys. 56, 2801 (1972).
6.W. C. Stwalley, Chem. Phys. Letters 7, 600 (1970).
7.This conclusion is confirmed by arguments utilizing the vibrational amplitude in the manner of W. C. Stwalley, J. Chem. Phys. 56, 680 (1972).
8.R. J. Le Roy, Can. J. Phys. 50, 953 (1972).
9.The error estimate is obtained by adding the uncertainty in to half the standard errors in the mean experimental values.
10.J. A. Barker, R. A. Fisher, and R. O. Watts, Mol. Phys. 21, 657 (1971). I am grateful to Dr. Barker for correspondence which brought this reference to my attention.
11.G. C. Maitland and E. B. Smith, Mol. Phys. 22, 861 (1971).
12.M. Cavallini, G. Gallinaro, L. Meneghetti, G. Scoles, and U. Valbusa, Chem. Phys. Letters 7, 303 (1970).
13.J. M. Parson, P. E. Siska, and Y. T. Lee, J. Chem. Phys. 56, 1511 (1972).
14.L. W. Bruch and I. J. McGee, J. Chem. Phys. 53, 4711 (1970).
15.C. T. Chen and R. D. Present, J. Chem. Phys. 54, 3645 (1971).
16.The present number of 9 levels was predicted more than a decade ago by D. E. Stogryn and J. O. Hirschfelder, J. Chem. Phys. 31, 1531 (1959).
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