Presentation + Paper
14 March 2023 Shining light on the photophysics of polymethine dyes with chalcogenopyrylium termini
Author Affiliations +
Abstract
Previous reports of chalcogenopyrylium polymethine dyes establish singlet oxygen yields as high as 12%. Our studies of these systems suggested that the current understanding of the excited state dynamics is incomplete. In fact, we observe no evidence for singlet oxygen generation across a range of experiments. We have carried out steady-state and pulsedlaser kinetic experiments on a family of fourteen dyes, including six novel dyes, selected to vary physical and electronic structure. We have changed the identity of the chalcogen between selenium and tellurium heteroatoms, phenyl, thiophene, tert-butyl substituents, and methine linker length. Excited-state lifetimes were obtained by femtosecond transient absorption spectroscopy. Lifetimes were all sub-300 picoseconds, suggesting rapid relaxation. Furthermore, we observed no evidence of any triplet transient processes; phosphorescence was only observed in samples at 77 K. Variable-temperature NMR experiments implicate rotation of the pyran ring about the methine backbone as a critical determinant of the dynamics of these dyes that distinguishes their photophysics from more rigid analogues.
Conference Presentation
© (2023) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Lauren E. Rosch, Matthew R. Crawley, Thomas N Rohrabaugh Jr., Trenton R. Ensley, Ryan M. O'Donnell, and Timothy R. Cook "Shining light on the photophysics of polymethine dyes with chalcogenopyrylium termini", Proc. SPIE 12418, Organic Photonic Materials and Devices XXV, 1241804 (14 March 2023); https://doi.org/10.1117/12.2650099
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KEYWORDS
Dyes

Oxygen

Electrodes

Absorption

Oxidation

Platinum

Femtosecond phenomena

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