Interaction of multiporphyrin systems with molecular oxygen in liquid solutions: Extra-ligation and screening effects

Steady-state and time-resolved studies indicate that for a sequence of porphyrin or chlorin chemical dimers Zn-cyclodimer → (ZnOEP)₂Ph → (ZnOEP)₂ → (ZnHTPP)₂ → (ZnOEChl)₂ with relative lowering of excited S₁- and T₁-states, the extra-ligation by pyridine (PYR) does not influence essentially on fluorescence parameters but leads to an increase of T₁-states non-radiative decay (the most pronounced for dimers with higher lying T₁-levels). For pyridinated dimers at 293 K T₁-states quenching by molecular oxygen depends on the spacer flexibility and donor-acceptor interactions with PYR. In self-assembled triads and pentads energy and electron transfer (within a few ps) takes place from Zn-dimers to pyridyl substituted porphyrin extra-ligand, H₂P, followed by the effective population of H₂P T₁-state. For these systems, bimolecular constants of H₂P T₁-states quenching by O₂ decrease by 1.4-1.8 times with respect to those found for individual monomeric porphyrins. This effect is explained by the screening action of a strongly quenched Zn-porphyrin dimer subunit limiting the access of oxygen molecule to the excited extra-ligand. © 2002 Elsevier Science B.V. All rights reserved

Steric interactions influence on electron transfer efficiency in meso-nitrophenylporphyrins and their chemical dimers

Steric interactions upon mono- and di-meso-phenyl substitution in octaethylporphyrins (OEP) and their chemical dimers with the phenyl spacer manifests itself in the dramatical T₁-state lifetimes shortening at 293 K (from ms down to μs in degassed toluene solutions) without any influence on spectral-kinetic parameters of S₀- and S₁-states. This effect is explained by non-planar dynamic conformations in excited T₁-states caused by the phenyl ring torsional librations around a single C-C bond. For meso-ortho-nitrophenyl substituted OEPs the S₁-state quenching is caused by the direct “through space” electron transfer to low-lying CT state while for the corresponding Pd-complexes the direct electron transfer takes place from the locally excited T₁-state. For the last two cases steric interactions provide the optimal geometry with high electronic coupling between porphyrin macrocycle and nitro-group

Manifestation of nonplanarity effects and charge-transfer interactions in spectral and kinetic properties of triplet states of sterically strained octaethylporphyrins

Properties of the triplet states of octaethylporphyrins with the steric hindrance (free bases and Pd complexes) are studied by the methods of stationary and kinetic spectroscopy in the temperature range from 77 to 293 K. The mono-mesophenyl substitution results in a decrease in the quantum yield and shortening of the phosphorescence lifetime of Pd complexes by 250–3500 times in degassed toluene at 293 K. The phosphorescence quenching is caused by nonplanar dynamic conformations of the porphyrin macrocycle in the T₁ state, which also lead to the appearance of new bands at λ ~ 1000 nm in the T—T absorption spectra. As the number of meso-phenyls (Pd-octaetyltetraphenylporphyrin) increases, the quantum yield of phosphorescence further decreases (<10⁻⁵) at 293 K, the lifetime of the T₁ state shortens (<50 ns), and the efficiency of the singlet oxygen generation abruptly decreases (<0.01). The intense bathochromic emission of this compound at 705 nm with a lifetime of 1 ms at 77 K is assigned to the phosphorescence of a nonplanar conformation. Upon meso-orthonitrophenyl substitution, the quenching of phosphorescence of Pd complexes (by more than 10⁴ times at 293 K) is caused by direct nonadiabatic photoinduced electron transfer from the T₁ state to the nearest charge-transfer state with the probability k_et^T = (1.5-4.0) × 10⁶ s⁻¹. The induced absorption of ortho-nitro derivatives in the region between 110 and 1400 nm is caused by mixing of pure ππ⃰ states with charge-transfer states. © 2001 MAIK “Nauka/Interperiodica”

Resonance Raman and FTIR spectra of Mg-porphyrazines

Resonance Raman spectra (RRS) of Mg-tetraazaporphyrin (1) and Mg-tetraazaoctaphenylporphyrin (2) in solid crystal powder at ambient temperature and different excitation wavelengths were recorded and analyzed. FTIR spectra of 1 and 2 in solid crystal powder were also measured. On the basis of DFT quantum-chemical calculations the frequencies, maximum amplitude changes for internal coordinates, and the symmetry of the normal modes were calculated. The analysis of the experimental data and the results of quantum-chemical calculations allow us to carry out the assignment of modes manifested in the Raman and IR-spectra of 1 and 2 to the calculated set of vibrations. Differences in the orientation of the aryl rings of 2 and their modes manifestation in the spectra were identified and compared to metalloporphyrins with phenyl groups in mesa-positions. An explanation for the spectral changes upon substitution in beta-positions of pyrrolic rings by phenyl units is given, providing further elucidation of the structural features arising upon progressive substitution by phenyl groups for the design of new types of dendrimers. (C) 2013 Elsevier B.V. All rights reserved