The steady-state and time-resolved fluorescence and H-1 NMR spectra of a st
ilbenesulphonic acid salt, commonly used as an optical brightening agent, w
as studied as a function of concentration in aqueous solution. The aggregat
es, formed at higher concentrations, were shown to be predominantly dimers
with the central stilbene moieties of the molecules stacked plane-parallel.
The equilibrium constant for the dimer formation at 25 degrees C was obtai
ned from both NMR and fluorescence measurements. Copyright (C) 1999 John Wi
ley & Sons, Ltd.