Abstract
Halogen bonding between a carbazole-based, pyridine-substituted organic semiconductor and a common halogen-bond donor (pentafluoroiodobenzene) yields efficient halogen-bond-driven fluorescence modulation in solution. Steady-state, time-resolved emission and absorption spectroscopy as well as density functional theory studies demonstrate that the fluorescence modulation arises from halogen-bond-induced intramolecular charge transfer. Fluorescence modulation offers a range of possibilities both in solution and in the solid state, for instance providing a potential pathway for the design of tunable luminescent materials for light-emitting devices.
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CITATION STYLE
Salunke, J. K., Durandin, N. A., Ruoko, T. P., Candeias, N. R., Vivo, P., Vuorimaa-Laukkanen, E., … Priimagi, A. (2018). Halogen-Bond-Assisted Photoluminescence Modulation in Carbazole-Based Emitter. Scientific Reports, 8(1). https://doi.org/10.1038/s41598-018-32830-3
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