Synthesis and characterization of 2-(anthracene-9-yl)-4,5-diphenyl-1-imidazole derivatives as environmentally sensitive fluorophores

• Published in: RSC advances 2024-07, Vol.14 (32), p.23511-23519
• Main Authors: Younes, Eyad A, AL-Snaid, Amneh M, Abu-Safieh, Kayed A, Salami, Fatemeh, Aljaar, Nayyef, Zhao, Yuming
• Format: Article
• ISSN: 2046-2069
• DOI: 10.1039/d4ra03735a

2-(Anthracene-9-yl)-4,5-diphenyl-1 H -imidazole (ADPI) provides an intriguing molecular platform for developing organic fluorophores with diverse properties and fluorescence performances. However, derivatives of ADPI have not yet been well explored and extensive studies are warranted. To shed more light on this, we have synthesized a series of π-extended ADPIs through a concise synthetic route involving an efficient cross-condensation reaction followed by Pd-catalyzed Suzuki cross-coupling. The obtained compounds were subjected to X-ray single crystallographic analysis to understand their molecular conformational and solid-state packing properties. Furthermore, UV-Vis absorption and fluorescence spectroscopic analyses were conducted. Our experimental results have disclosed interesting solvatofluorochromic properties of these compounds which are useful for solvent polarity-sensitive applications. The presence of an amphoteric imidazolyl group in the ADPI derivatives also renders them sensitive fluorescence responses to strong protic acids ( e.g. , trifluoroacetic acid) as well as fluoride anion. It transpires that the fluorescence changes are dependent on the functional groups attached to the ADPI core, suggesting a bottom-up molecular tuning approach for development of fluorophores and chemosensors with diverse functions. A series of π-extended 2-(anthracene-9-yl)-4,5-diphenyl-1 H -imidazole (ADPI) derivatives were synthesized. These compounds show sensitive fluorescence responses to solvent polarity, acidity, and fluoride anion.