PHOTOPHYSICS OF TRIPHENYLPHOSPHINES AND THEIR OXIDES - ROLE OF DIMETHYLAMINO SUBSTITUENTS

Steady-state and time-resolved spectroscopy experiments with picosecon d or subpicosecond resolution are carried out in order to clarify the anomalous fluorescence properties of solutions prepared with triphenyl phosphine compounds in various non-deaerated solvents at room temperat ure. Evidence is given for the formation of triphenylphosphine oxides in the solutions and for the coexistence of the oxidized and non-oxidi zed forms at the concentrations used for time-resolved experiments. Th e photoinduced formation of an emissive charge-transfer state, previou sly reported for solutions prepared with the dimethylamino substituted triphenylphosphines, is shown to be due to the corresponding oxide wh ich exhibits a dual fluorescence with large solvatochromism. The non-o xidized forms of both the dimethylamino substituted and unsubstituted triphenylphosphines are found to exhibit a strongly red-shifted emissi on band with little solvatochromism. A photoinduced geometrical change with an increase of the conjugation in the excited state is proposed to explain this observation. On the other hand, an extra fluorescence band occuring at shorter wavelengths for the non-oxidized dimethylamin o-substituted compound is not completely understood. (C) 1997 Elsevier Science B.V.