Practicable Syntheses of Electroluminescent Ionic 2,2′‐Bifluorenes

Abstract The development of a practicable library synthesis of ionic 2,2′‐bifluorenes is described that improves the safety and reduces waste associated with the ubiquitous method of preparing these and related electroluminescent compounds. Additionally, an X‐ray crystal structure that reveals how triflate counterions can provide a second link between the alkylimidazolium subunits and the photoluminescent core is presented.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-10-16
DOI
https://doi.org/10.1002/ejoc.202400976
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Practicable Syntheses of Electroluminescent Ionic 2,2′‐Bifluorenes

Simon John Coles, Isabelle Chataigner, Steve Beeby, Katie L. Court et al.
European Journal of Organic Chemistry
Fluorine in Organic Chemistry
article

Practicable Syntheses of Electroluminescent Ionic 2,2′‐Bifluorenes

Simon John Coles, Isabelle Chataigner, Steve Beeby, Katie L. Court, Mark E. Light, Oliver J. Ward, Robert C. Carroll, Julien Legros, Yi Li
article en

Abstract

Abstract The development of a practicable library synthesis of ionic 2,2′‐bifluorenes is described that improves the safety and reduces waste associated with the ubiquitous method of preparing these and related electroluminescent compounds. Additionally, an X‐ray crystal structure that reveals how triflate counterions can provide a second link between the alkylimidazolium subunits and the photoluminescent core is presented.

European Journal of Organic ChemistryVol. 27(48)
Centre National de la Recherche Scientifique (FR), Normandie Université (FR), Laboratoire COBRA (FR), University of Southampton (GB), Université de Rouen Normandie (FR), Institut National des Sciences Appliquées Rouen Normandie (FR)
Engineering and Physical Sciences Research Council, European Regional Development Fund, Interreg
Openalex Percentile: Top 86%
Fluorine in Organic Chemistry
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