M. Mac, FLUORESCENCE QUENCHING OF 1-CYANONAPHTHALENE BY IODIDE AND THIOCYANIDE ANIONS IN POLAR-SOLVENT, Bulletin of the Polish Academy of Sciences. Chemistry, 45(1), 1997, pp. 53-61
Fluorescence quenching of 1-cyanonaphthalene (1-CNN) by iodide and thi
ocyanide anions in ethanol, acetonitrile, water and in water solution
of 0.02 M beta-cyclodextrin has been investigated. The mechanism of th
e fluorescence quenching of 1-CNN by inorganic anions is the electron
transfer from the anion to the excited 1-CNN molecule, confirmed previ
ously by nanosecond transient absorption measurements. The Stern-Volme
r plots exhibit the positive curvatures, indicating relatively strong
diffusion Limitation of the quenching process. Diffusion coefficients
and encounter radii for the investigated systems were calculated from
the nonlinear Stern-Volmer dependencies using the procedure by Stevens
. It has been found that mutual diffusion coefficients are in agreemen
t with those taken from other published sources. Both the diffusion co
efficients and encounter radii estimated for the systems containing 1-
CNN complexed with beta-cyclodextrin are similar to those in ethanol,
which indicates similarity of cyclodextrin cavities to ethanol.