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Halogen-Bond-Assisted Photoluminescence Modulation in Carbazole-Based Emitter.


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.

SUBMITTER: Salunke JK 

PROVIDER: S-EPMC6158238 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

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Halogen-Bond-Assisted Photoluminescence Modulation in Carbazole-Based Emitter.

Salunke Jagadish K JK   Durandin Nikita A NA   Ruoko Tero-Petri TP   Candeias Nuno R NR   Vivo Paola P   Vuorimaa-Laukkanen Elina E   Laaksonen Timo T   Priimagi Arri A  

Scientific reports 20180926 1


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  ...[more]

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