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Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores.


ABSTRACT: Benzimidazole-based boranils were designed and synthesized in order to assess the influence of halogen substituents on their optoelectronic properties. All compounds are photoluminescent in solution and solid state. Compared to the free ligands, the new boranils emit at a lower wavelength, by elimination of the excited-state intramolecular proton transfer observed with the ligands. In the solid state, some of the boranils exhibit a deep blue emission, presenting Commission Internationale de l'Éclairage (CIE) coordinates with an x-component of less than 0.16 and a y-component smaller than 0.04, highly desired values for the development of blue emitting materials.

SUBMITTER: Vaz PAAM 

PROVIDER: S-EPMC8348718 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature

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Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores.

Vaz Patrícia A A M PAAM   Rocha João J   Silva Artur M S AMS   Guieu Samuel S  

Materials (Basel, Switzerland) 20210731 15


Benzimidazole-based boranils were designed and synthesized in order to assess the influence of halogen substituents on their optoelectronic properties. All compounds are photoluminescent in solution and solid state. Compared to the free ligands, the new boranils emit at a lower wavelength, by elimination of the excited-state intramolecular proton transfer observed with the ligands. In the solid state, some of the boranils exhibit a deep blue emission, presenting Commission Internationale de l'Éc  ...[more]

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