The fluorescence quenching of some substituted naphthalenes by chlorom
ethanes such as carbontetrachloride (CCl4), chloroform (CKCl3) and dic
hloromethane (CH2Cl2) have been studied in a large number of solvents
in room temperature. The quenching rate constants (k(q)) have been det
ermined for all the fluorophores in all the solvents. For CCl4 quenchi
ng the k(q) depends on solvent viscosity whereas for CHCl3 and CH2Cl2
it depends neither on solvent viscosity nor on solvent polarity. From
the results the quenching mechanism is explained in terms of an encoun
ter complex formation for CCl4 quenching and an intermediate donor-acc
eptor complex formation for CHCl3 and CH2Cl2 quenching in the excited
state.