A New Protocol for the Synthesis of New Thioaryl-Porphyrins Derived from 5,10,15,20-Tetrakis(pentafluorophenyl)porphyrin: Photophysical Evaluation and DNA-Binding Interactive Studies
Patrícia Foletto,
Fabiula Correa,
Luciano Dornelles,
Bernardo A. Iglesias,
Carolina H. da Silveira,
Pablo A. Nogara,
João B. T. da Rocha,
Maria A. F. Faustino,
Oscar E. D. Rodrigues
Affiliations
Patrícia Foletto
Departamento de Química, Universidade Federal de Santa Maria, Santa Maria-RS 97105-900, Brazil
Fabiula Correa
Departamento de Química, Universidade Federal de Santa Maria, Santa Maria-RS 97105-900, Brazil
Luciano Dornelles
Departamento de Química, Universidade Federal de Santa Maria, Santa Maria-RS 97105-900, Brazil
Bernardo A. Iglesias
Laboratório de Bioinorgânica e Materiais Porfirínicos, Departamento de Química, Universidade Federal de Santa Maria–UFSM, Santa Maria–RS 97105-900, Brazil
Carolina H. da Silveira
Laboratório de Bioinorgânica e Materiais Porfirínicos, Departamento de Química, Universidade Federal de Santa Maria–UFSM, Santa Maria–RS 97105-900, Brazil
Pablo A. Nogara
Laboratório de Bioquímica Toxicológica, Departamento de Bioquímica e Biologia Molecular, Univerisidade Federal de Santa Maria, Santa Maria–RS 97105-900, Brazil
João B. T. da Rocha
Laboratório de Bioquímica Toxicológica, Departamento de Bioquímica e Biologia Molecular, Univerisidade Federal de Santa Maria, Santa Maria–RS 97105-900, Brazil
Maria A. F. Faustino
QOPNA and Department of Chemistry, University of Aveiro, Aveiro 3810-193, Portugal
Oscar E. D. Rodrigues
Departamento de Química, Universidade Federal de Santa Maria, Santa Maria-RS 97105-900, Brazil
A new protocol for the preparation of thioaryl-porphyrins is described. The compounds were prepared from different disulfides employing NaBH4 as a reducing agent. The methodology allowed the preparation of four different thioaryl-porphyrins in very-good to excellent yields under soft conditions, such as short reaction times and smooth heating. Additionally, the photophysical properties of new compounds were determined and experimental and theoretical DNA interactions were assessed.