Photophysics and spectroscopy of the higher electronic states of zinc metalloporphyrins: a theoretical and experimental study

Abstract

The photophysics of the S₂ and S₁ excited states of zinc porphyrin (ZnP) and five of its derivatives (ZnOEP, ZnTBP, ZnTPP, ZnTFPP, ZnTCl₈PP) have been investigated by measuring their steady-state absorption and fluorescence spectra, quantum yields and excited state lifetimes at room temperature in several solvents. The radiative and radiationless decay constants of the fluorescent excited states accessible in the visible and near UV regions of the spectrum have been obtained. Despite the similarities in the Soret spectra of these compounds, their S₂ excited state radiationless decay rates differ markedly. Although the S₂–S₁ electronic energies of a given zinc porphyrin vary linearly with the Lippert (refractive index) function of the solvent, the S₂ radiationless decay rates of the set of compounds do not follow the energy gap law of radiationless transition theory. Calculations, using time-dependent density functional theory (TDDFT), of the energies and symmetries of the complete set of excited states accessible by 1- or 2-photon absorption in the near UV-visible have also been carried out. Substitution on the porphyrin macrocycle framework affects the ground state geometry and alters the electron density distributions, the orbital energies and the relative order of the excited electronic states accessible in the near UV-blue regions of the spectrum. The results are used to help interpret both the nature of the electronic transitions in the Soret region, and the relative magnitudes of the radiationless transition rates of the excited states involved.