Density functional theory (DFT) electronic structure calculations were carried out to predict the structures and ground-state spectra for zinc complexes of porphyrin (ZnP), tetraazaporphyrin (ZnTAP), tetrabenzoporphyrin (ZnTBP), and phthalocyanine (ZnPc). All four porphyrins are found to have stable D4h structures. Structurally, meso-tetraaza substitutions significantly reduce the central hole in ZnTAP and ZnPc compared to ZnP. The excitation energies and oscillator strengths, computed by time-dependent DFT, provide a good account of the observed spectra of all four compounds. The TDDFT spectrum of ZnPc has a number of bands in the Soret region, in agreement with the experimental spectra that have been determined through spectral deconvolution. The low energy n→π* transition (Q′) reported for ZnPc, however, was not found in the computed spectrum. The effects of meso-tetraaza substitutions and tetrabenzo annulations on the spectrum of ZnP are discussed.
No takes yet. Share an insight, caveat, or question.
Nguyen et al. (2001) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: