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Stark effect expectation values

On the basis of these formulae one can convert measurements of area, which equals the integral in the latter formula, under spectral lines into values of coefficients in a selected radial function for electric dipolar moment for a polar diatomic molecular species. Just such an exercise resulted in the formula for that radial function [129] of HCl in formula 82, combining in this case other data for expectation values (0,7 p(v) 0,7) from measurements of the Stark effect as mentioned above. For applications involving these vibration-rotational matrix elements in emission spectra, the Einstein coefficients for spontaneous emission conform to this relation. [Pg.299]

The dipole moments of the oxazole molecule determined by dielectric218 and Stark-effect measurements in the microwave spectrum233 are 1.4 and 1.5 0.1 D, respectively. On the basis of small inertial defects in oxazole, Mackrodt et al.m have concluded that the molecule is planar. There is a complete lack of data on the dipole moment of simple alkyl-substituted oxazoles. On the other hand, the values of the dipole moments of a number of aryl-substituted oxazoles have been reported (see Table V). As might be expected, a nitro substituent into the para position of a phenyl ring attached to oxazole increases the value of dipole moment by 2.0-3.5 D. [Pg.158]


See other pages where Stark effect expectation values is mentioned: [Pg.297]    [Pg.308]    [Pg.316]    [Pg.526]    [Pg.150]    [Pg.6113]    [Pg.461]    [Pg.141]    [Pg.351]    [Pg.41]    [Pg.6112]    [Pg.34]    [Pg.116]    [Pg.252]    [Pg.203]    [Pg.234]    [Pg.87]    [Pg.34]    [Pg.609]    [Pg.150]    [Pg.157]    [Pg.207]    [Pg.294]   
See also in sourсe #XX -- [ Pg.14 ]




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