A Singlet Oxygen Photogeneration and Luminescence Study of Unsymmetrically Substituted Mesoporphyrinic Compounds

• Main Authors: Anabela Sousa Oliveira, Dumitru Licsandru, Rica Boscencu, Radu Socoteanu, Veronica Nacea, Luis Filipe Vieira Ferreira
• Format: Article
• Language: English
• Published: Hindawi Limited 2009-01-01
• Series: International Journal of Photoenergy
• Online Access: http://dx.doi.org/10.1155/2009/413915
• ISSN: 1110-662X; 1687-529X

This paper deals with a series of new unsymmetrically substituted mesoporphyrins: 5-(2-hydroxyphenyl)-10,15,20-tris-phenyl-21,23-H-porphyrin (TPPOHO), 5-(3-hydroxyphenyl)-10,15,20-tris-phenyl-21,23-H-porphyrin (TPPOHM), 5-(4-hydroxyphenyl)-10,15,20-tris-phenyl-21,23-H-porphyrin (TPPOHP), 5-(2-hydroxyphenyl)-10,15,20-tris-butyl-21,23-H-porphyrin (TBPOHO), and their parent nonsubstituted compounds, respectively, 5,10,15,20-tetrakis-phenyl-21,23-H-porphyrin (TPP) and 5,10,15,20-tetrakis-butyl-21,23-H-porphyrin (TBP). Several photophysical studies were carried out to access the influence of the unsymmetrical substitution at the porphyrinic macrocycle on porthyrin's photophysical properties, especially porthyrin's efficiency as singlet oxygen sensitizers. The quantum yields of singlet oxygen generation were determined in benzene (ΦΔ(TPP) = 0.66 ± 0.05; ΦΔ(TPPOHO) = 0.69 ± 0.04; ΦΔ(TPPOHM) = 0.62 ± 0.04; ΦΔ(TPPOHP) = 0.73 ± 0.03; ΦΔ(TBP) = 0.76 ± 0.03; ΦΔ(TBPOHO) = 0.73 ± 0.02) using the 5,10,15,20-tetraphenyl-21,23-H-porphine (ΦΔ(TPP) = 0.66) and Phenazine (ΦΔ(Phz) = 0.83) as reference compounds. Their fluorescence quantum yields were found to be (Φf(TPPOHO) = 0.10 ± 0.04; Φf(TPPOHM) = 0.09 ± 0.03; Φf(TPPOHP) = 0.13 ± 0.02; Φf(TBP) = 0.08 ± 0.03 and Φf(TBPOHO) = 0.08 ± 0.02 using 5,10,15,20-tetraphenyl-21,23-H-porphine as reference Φf(TPP) = 0.13). Singlet state lifetimes were also determined in the same solvent. All the porphyrins presented very similar fluorescence lifetimes (mean values of τS (with O2, air equilibrated) = 9.6 ± 0.3 nanoseconds and (without O2, argon purged) = 10.1 ± 0.6 nanoseconds, resp.). The phosphorescence emission was found to be negligible for this series of unsymmetrically substituted mesoporphyrins, but an E-type, thermally activated, delayed fluorescence process was proved to occur at room temperature.