Abstract
Order parameters determined by different spectroscopic methods are not identical because they refer to different “pseudo” orientation axes if an orientational distribution function f=f (β, γ) holds. The angles between these axes and those referring to the system of principal axes of the orientational distribution coefficients go ij33are determined by the molecular properties owing to the spectroscopic method used. This is shown by an analysis of the frequency and temperature dependence of a relative order parameter for testosterone propionate in cholesteryl chloride/cholesteryl laurate measured with ultraviolet absorption (UV) and circular dichroism (ACD) as an e xamp1e.