A description of time-resolved polarized fluorescence spectroscopy on
the fluorophores incorporated into uniaxially organized molecular medi
a and undergoing different ground- and excited-state aligning interact
ions, is discussed. The excited-state aligning-potential-restricted ro
tational diffusion model is considered. From the solution of the motio
n equation the time-evolution of even and odd higher-rank molecular or
der parameters can be recovered. This enables more precise reconstruct
ion of the angular distribution of fluorophores aligned in electric fi
eld, adsorbed at the solid(liquid)/air surfaces and at the solid(liqui
d)/liquid interfaces and also aligned in membranes, liquid crystals an
d Langmuir-Blodgett films. (C) 1998 Elsevier Science B.V.