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

Author:

Oliveira Anabela Sousa1,Licsandru Dumitru2,Boscencu Rica3,Socoteanu Radu4,Nacea Veronica3,Vieira Ferreira Luis Filipe1

Affiliation:

1. Centro de Química-Física Molecular (CQFM) and Instituto de Nanociencias e Nanotecnologias (IN), Instituto Superior Técnico, Universidade Técnica de Lisboa, Avenida Rovisco Pais, 1049-001 Lisbon, Portugal

2. Department of Physical Chemistry, Faculty of Chemistry, University of Bucharest, 4-12 Regina Elisabeta Bulevardul, 030018 Bucharest, Romania

3. Department of Inorganic Chemistry, Faculty of Pharmacy, “Carol Davila” University of Medicine and Pharmacy, Bucharest, 6 Traian Vuia Street, Sector 1, Bucharest, Romania

4. Institute of Physical Chemistry “I.G. Murgulescu” of the Romanian Academy, 202 Spl. Independentei, 060021 Bucharest-12, Romania

Abstract

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 andΦf(TBPOHO) = 0.08 ± 0.02 using 5,10,15,20-tetraphenyl-21,23-H-porphine as referenceΦf(TPP) = 0.13). Singlet state lifetimes were also determined in the same solvent. All the porphyrins presented very similar fluorescence lifetimes (mean values ofτS(withO2, air equilibrated) = 9.6 ± 0.3 nanoseconds and (withoutO2, 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.

Funder

Fundação para a Ciência e a Tecnologia

Publisher

Hindawi Limited

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment,Atomic and Molecular Physics, and Optics,General Chemistry

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