The photophysical properties of the triethylammonium salt of sulfoprop
yl)-5,5'-dichloro-9-ethylthiacarbocyanine (THIATS) and other related d
yes have been studied by means of steady-state and time-resolved spect
roscopic techniques. Absorption and fluorescence maxima and bandwidths
suggest, together with NMR data, the existence of more than one groun
d-state conformation for this dye. Analysis of the fluorescence decays
by time-correlated single-photon counting and time-resolved fluoresce
nce spectroscopy further supports the steady-state spectroscopy result
s. An additional short-lived fluorescent species is observed in some p
olar solvents such as methanol and I-octanol. The dependence of the sp
ectral features and the fluorescence kinetics on the nature of the sol
vent is explained by a model invoking ion-pairing and conformational c
hanges in the ground state of the dye. It is shown that polarity and p
olarizability of the solvent control the photophysical properties of T
HIATS.