Aromatically π-extended porphyrins
possess exceptionally
intense one-photon (1P) and sometimes two-photon (2P) absorption bands,
presenting interest for construction of optical imaging probes and
photodynamic agents. Here we investigated how breaking the molecular
symmetry affects linear and 2PA properties of π-extended porphyrins.
First, we developed the synthesis of porphyrins fused with two phthalimide
fragments, termed syn-diarylphthalimidoporphyrins
(DAPIP). Second, the photophysical properties of H2, Zn,
Pd, and Pt DAPIP were measured and compared to those of fully symmetric
tetraarylphthalimidoporphyrins (TAPIP). The data were interpreted
using DFT/TDDFT calculations and sum-over-states (SOS) formalism.
Overall, the picture of 2PA in DAPIP was found to resemble that in
centrosymmetric porphyrins, indicating that symmetry breaking, even
as significant as by syn-phthalimido-fusion, induces
a relatively small perturbation to the porphyrin electronic structure.
Collectively, the compact size, versatile synthesis, high 1PA and
2PA cross sections, and bright luminescence make DAPIP valuable chromophores
for construction of imaging probes and other bioapplications.