Fast and Tunable Phosphorescence from Organic Ionic Crystals
Partanen, I., Al-Saedy, O., Eskelinen, T., Karttunen, A. J., Saarinen, J. J., Mrózek, O., Steffen, A., Belyaev, A., Chou, P.-T., & Koshevoy, I. O. (2023). Fast and Tunable Phosphorescence from Organic Ionic Crystals. Angewandte Chemie, 62(36), Article e202305108. https://doi.org/10.1002/anie.202305108
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Angewandte ChemieAuthors
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2023Copyright
© 2023 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH
Crystalline diphosphonium iodides [MeR2P–spacer–R2Me]I with phenylene (1, 2), naphthalene (3, 4), biphenyl (5) and anthracene (6) as aromatic spacers, are photoemissive under ambient conditions. The emission colors (λem values from 550 to 880 nm) and intensities (Φem reaching 0.75) are defined by the composition and substitution geometry of the central conjugated chromophore motif, and the anion–π interactions. Time-resolved and variable-temperature luminescence studies suggest phosphorescence for all the titled compounds, which demonstrate observed lifetimes of 0.46–92.23 μs at 297 K. Radiative rate constants kr as high as 2.8 × 105 s–1 deduced for salts 1–3 were assigned to strong spin-orbit coupling enhanced by an external heavy atom effect arising from the anion–π charge-transfer character of the triplet excited state. These rates of anomalously fast metal-free phosphorescence are comparable to those of transition metal complexes and organic luminophores that utilize triplet excitons via a thermally activated delayed fluorescence mechanism, making such ionic luminophores a new paradigm for the design of photofunctional and responsive molecular materials.
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Otto A. Malm FoundationFunding program(s)
FoundationAdditional information about funding
Financial support from the Academy of Finland (decision 351618, I.O.K.; decision 340584, T.E. and A.J.K.; decision 339544, J.J.S.; Flagship Programme, Photonics Research and Innovation PREIN, decision 320166), Alexander von Humboldt and Otto A. Malm Foundations (A.B.), and the National Science and Technology Council (NSTC), Taiwan, are gratefully acknowledged.License
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