The use of organic nanomaterials in biomedical and optical devices has been widely studied. The key to improving the performance and stability of these devices is to control the fabrication process, which determines the phase stability and photophysical properties. In this study, fluorescence changes were observed during the reprecipitation process of mechanofluorochromic molecules of dibenzoyl(methanato)boron difluoride. The cyan-emission phase (C-phase) was first identified. The time evolution of the resolved fluorescence spectra revealed that the green-emission phase (G-phase) was formed from the amorphous phase with yellow emission via the C-phase, in addition to the direct formation of the G-phase. Combined with the results of the investigation into the thermal properties, the fluorescence changes clearly indicate a two-step nucleation process and Ostwald's rule of stages for polymorph transition, which enables us to not only provide guidance for controlling the fabrication process but also propose the ripening process for organic nanoparticle formation.
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http://dx.doi.org/10.1002/cphc.202100370 | DOI Listing |
Luminescence
August 2024
College of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, China.
A pair of 1,8-naphthalimides (NPIs) were designed and successfully synthesized through embellishing amino-containing NPI with 4-diethylaminosalicyladehyde and 4-diethylaminobenzaldehyde, respectively. Their structures were fully confirmed by H/C NMR, HR-MS and FT-IR spectroscopic studies. Their photophysical properties were systematically investigated in different solvents of varied polarity, in THF/water mixtures with varying water fractions (f), and in THF solvent with varying concentrations of NPIs.
View Article and Find Full Text PDFChem Asian J
August 2024
State Key Laboratory of Green Pesticide, Central China Normal University, Wuhan, 430079, PR China.
In this study, we have successfully designed and synthesized two novel dual-emission emitters featuring phenothiazine-5-oxide and phenothiazine-5,5-dioxide motifs, characterized by highly lopsided and asymmetric conformational states. Through rigorous spectral examinations and DFT calculations, the compounds exhibit distinctive ICT phenomena, coupled with efficient emission in solid states and AIEE characteristics under high water fractions in DMF/HO mixtures. These non-planar luminogens exhibit vibrant green and blue solid-state luminescence, with fluorescence quantum yields of 24.
View Article and Find Full Text PDFLuminescence
April 2024
Physical and Chemical Inspection Center, Dali Institute for Food Control, Dali, P.R. China.
To further explore the relationship between aryl substituents and mechanofluorochromic (MFC) behaviors, four salicylaldimine-based difluoroboron complexes (ts-Ph BF, ts-Ph-NA BF, ts-2NA BF, and ts-triphenylamine [TPA] BF), including aromatic substituents with different steric hindrance effects, were designed and successfully synthesized. Four complexes with twisted molecular conformation displayed intramolecular charge transfer and aggregation-induced emission properties. Under external mechanical stimuli, the as-synthesized powders of ts-Ph BF, ts-Ph-NA BF, and ts-TPA BF exhibited redshift fluorescence emission behaviors, and ts-Ph BF and ts-TPA BF could be recovered to original shifts by fuming, but ts-Ph-NA BF displayed irreversible switching.
View Article and Find Full Text PDFSci Adv
February 2024
National Key Laboratory of Green Pesticide, College of Chemistry, Central China Normal University, Wuhan 430079, People's Republic of China.
Achieving high-contrast tricolor emissive regulation of a single-component molecule using a single type of external stimulus is highly desirable but challenging. In the present study, we report a symmetric acceptor-donor-acceptor (A-D-A)-type aggregation-induced emission-active luminogen, which displays a sequential high-contrast fluorescence switching just by anisotropic mechanical grinding. Specifically, upon light grinding, an orange-yellow-to-blue hypsochromic mechanofluorochromic response with a distinct color contrast (change in the maximum emission wavelength, Δλ = 122 nm) is noticed, and the slightly ground solid exhibits a blue-to-red high-contrast (Δλ = 185 nm) bathochromic mechanofluorochromic conversion upon vigorous grinding.
View Article and Find Full Text PDFJ Mater Chem C Mater
February 2024
Université Paris-Saclay, ENS Paris-Saclay, CNRS, PPSM 4 Avenue des Sciences 91190 Gif-sur-Yvette France
A family of (alkylsilyl)pyrene-1-carboxamides exhibits similar mechanofluorochromic responses upon grinding. However, their spontaneous fluorescence recovery processes are distinct despite their similarity in chemical structures and crystal packings. Fluorescence spectroscopy, crystallography, and nanomechanical tests revealed that the chromic direction is dominated by the packing motif, while the fluorescence recovery is driven by the intermolecular interactions and the reversibility of deformation.
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