Photophysical properties of 5-hydroxyindole (5HI): Laser flash photolysis study

Steady state fluorescence emission and transient absorption spectra of 9-fluorenone (9FL) were measured in the presence of 5-hydroxyindole (5HI) in highly polar acetonitrile (ACN) environment at ambient temperature. Cyclic voltammetry measurements demonstrate that ground state 5HI as a donor could take part in highly exothermic electron transfer (ET) reactions with excited 9FL, which should serve as electron acceptor. From the transient absorption measurements it is inferred that in geminate ion-pair (GIP) (or contact ion pair), formed initially due to photoinduced ET, the decay of this contact ion-pair occurs not only through ion recombination (back electron transfer to ground state of reactants), but through the other processes also such as proton-transfer (hydrogen abstraction) from radical cation to anion and separation of ion-pair producing the free ions. From the computed reorganisation energy parameter (λ) and experimentally observed -‡ _ET ⁰ values it is hinted that there is a possibility that highly exothermic forward electron transfer reactions in the singlet stateS ₁ occur, within present reacting systems, in Marcus inverted region. Back transfer seems to follow the same path. Investigations with similar other reacting systems are underway.