The photophysics of Ni(II) meso-tetraphenylbenzoporphyrin: A combined theoretical and experimental investigation

Abstract

A combined theoretical and kinetic spectrometric investigation of Ni(II)-tetraphenyl tetrabenzoporphyrin (NiTPTBP) has demonstrated that photo-excitation into the B band (400 nm) of the ground state absorption spectrum rapidly generates the compound in its Q state. The intriguing time dependence of stimulated emission generated from the Q state implies that this state is populated via two (or more) radiationless channels, one is very rapid (<1 ps) and another less rapid (∼6 ps). The theoretical results show that two excited states with significant oscillator strengths lie close in energy within the B band envelope. These are the 5 1E (2.72 eV; f = 0.95) and the 4 1E (2.63 eV; f = 0.19) and both these could be directly excited by the 400 nm excitation pulse, in which case these two upper states could be the origins of the two kinetic populations of the Q state. Less than 2 ps post excitation onset the spectral characteristics of a hot metal-centered excited state appear, identified as 2 1E. The excess vibrational energy of this state is dissipated by IVR and intermolecular modes. Eventually the cooled (d,d) state repopulates the initial ground state with a rate that is extremely solvent dependent. The 2 1E state is computed to possess some 20% of MLCT character, which is the possible source of the solvent dependent deactivation rate.