Femtosecond transient absorption studies of charge-transfer complexes
of I, with hexamethylbenzene have been performed in a series of noncom
plexing solvents. Anisotropy measurements of the bleach of the charge-
transfer absorption band indicate that the geometry and electronic str
ucture of the complex is dependent upon the solvent environment. The r
esults are interpreted as favoring an oblique, nearly axial, geometry
in alkanes and a resting geometry in chlorinated methanes.