Tryptanthrin from indigo: Synthesis, excited state deactivation routes and efficient singlet oxygen sensitization

• Autor(a) principal: Pinheiro, Daniela
• Data de Publicação: 2020
• Outros Autores: Piñeiro, Marta, Pina, João, Brandão, Pedro, Galvão, Adelino M., Melo, J. Sérgio Seixas de
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• DOI: 10.1016/j.dyepig.2019.108125
• Texto Completo: http://hdl.handle.net/10316/91076; https://doi.org/10.1016/j.dyepig.2019.108125
• topic: Indigo; Tryptanthrin; Fluorescence; Singlet oxygen sensitization; TDDFT

The microwave-assisted synthesis of tryptanthrin from indigo in mild oxidation conditions, and a comprehensive study of the excited state properties of this compound in a variety of solvents with different polarity and viscosity values at room and low temperatures are reported. In contrast with indigo, emission of the triplet state of tryptanthrin is observed with a very efficient singlet oxygen sensitization quantum yield, indicating that the triplet state is efficiently populated. From time-resolved fluorescence and femtosecond transient absorption data, further supported with time-dependent density functional theory (TDDFT) calculations, two species, with S1 states with locally excited (LE) of π,π* nature and a charge transfer (CT) of n,π* characteristics, originated from an initially populated Frank-Condon S2 state (π,π*), are observed. The two electronically independent species are energetically nearly degenerate and inter-conversion is predicted (and rate constants determined) to occur between LE (S1) and CT (S1) species. Due to the low value of the fluorescence quantum yield (~10−3) and high triplet state yield (ϕT≥ϕΔ), the high stability of this compound is associated to the high efficiency of the radiationless deactivation processes which involve the formation of the CT state which efficiently converts, through S1 ~~> Tn intersystem crossing, to the T1 triplet state.