Nino Russo

The modulation of the photophysical properties of di‐substituted porphyrin rings upon the oxygen and sulfur‐for‐nitrogen replacement has been investigated at density functional theory (DFT) and its time‐dependent formulation (TDDFT). The considered properties range from structural behaviors and excitation energies to spin‐orbit coupling (SOC) and nonradiative intersystem kinetic constants. Results show that the SOC strongly increase upon chalcogen substitution and, accordingly, the computed nonradiative kinetic constant also indicate an efficient singlet‐triplet intersystem crossing in the sulfur containing macrocycle. The presented results indicate an alternative way to properly modulate the porphyrin's crucial properties for their use in photodynamic therapy, without resorting to the use of heavy atoms.