1. Methoxy substituent facilitated wide solvatofluorochromism, white light emission, polymorphism and stimuli-responsive fluorescence switching in donor-π-acceptor.
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Gayathri, Parthasarathy, Nantheeswaran, Periyappan, Mariappan, Mariappan, Karthikeyan, Subramanian, Pannipara, Mehboobali, Al-Sehemi, Abdullah G., Moon, Dohyun, and Anthony, Savarimuthu Philip
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TRIPHENYLAMINE , *INTRAMOLECULAR charge transfer , *FLUORESCENCE , *MOLECULAR conformation , *SINGLE molecules , *CRYSTAL lattices - Abstract
Methoxy substitution at acceptor end of TPA-acetophenone fluorophore showed white light emission, tunable emission by morphological transformation and mechano-responsive reversible fluorescence switching. [Display omitted] • White light emission from single fluorophore by methoxy substitution. • Tunable fluorescence by methoxy substitution and morphological transformation. • Fluorescent polymorphs with tunable emission. • Stimuli-responsive reversible and self-reversible fluorescence switching. Introducing methoxy substituent into triphenylamine-acetophenone based donor-π-acceptor fluorophore, 3-(4-(diphenylamino)phenyl)-1-phenylprop-2-en-1-one (1), produced strong solvatofluorochromism including white light emission, fluorescent polymorphs and mechano-responsive fluorescence switching. The unsubstituted and methoxy substituted compounds displayed strong solvent polarity mediated tunable emission in the solution. Interestingly, 3-(4-(diphenylamino)phenyl)-1-(4-methoxyphenyl)prop-2-en-1-one (2) and 3-(4-(diphenylamino)-2-methoxyphenyl)-1-(4-methoxyphenyl)prop-2-en-1-one (3) showed single molecule white light emission in DMSO and ethanol, respectively. 1-3 exhibited strong green/yellow fluorescence in the solid-state (Quantum yield (Φ f) = 10 to 23%). 2 produced fluorescent polymorphs (green (2-G) and yellow (2-Y). Single crystal structural analysis revealed that donor and acceptor phenyl units adopted coplanar conformation in 2-G and 3 whereas twisted molecular conformation in 1 and 2-Y. Further, 2-G exhibited π...π interactions facilitated isolated dimers whereas 2-Y showed well separated molecules in the crystal lattice. Aggregation induced emission (AIE) studies showed morphological transformation induced fluorescence tuning for 2. The intramolecular charge transfer (ICT) from TPA to acetophenone was confirmed by computational studies. Mechanofluorochromic (MFC) studies of 1 showed only slight reduction of intensity without modulating fluorescence wavelength significantly but 2 and 3 exhibited visible emissive colour change from yellow to green and vice versa by crushing and heating. Both 2 and 3 also exhibited self-reversible fluorescence switching that was confirmed by PXRD pattern. Thus, methoxy group introduction resulted in obtaining white light emitting fluorescence molecules in the solution state and self-reversible fluorescence switching materials. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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