One D-A type cruciform luminophore MDCS-BC based on carbazole has been prepared. We observed that this compound exhibits unique intramolecular charge-transfer (ICT) and typical aggregation-induced enhanced emission (AIEE) properties with the solid-state luminescence efficiency of 0.184. Moreover, this luminophore shows a significant stimuli-induced emission enhancement and chromism effect with good reversibility. Upon grinding, the fluorescence color of the as-prepared samples can change from blue (454 nm) to green (504 nm). What is unexpected is that the fluorescence efficiency of the initial powder is dramatically increased from 0.184 to 0.424 upon grinding. The results of PXRD, DSC and spectral properties studies show that the mechanical force-induced luminescence enhancement and chromism behavior of MDCS-BC originates from the transition between crystal and amorphous morphology, and the large red-shift and the emission enhancement inducing by grinding may be attributed to the planarization of the molecular conformation and subsequent planar ICT process.
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http://dx.doi.org/10.1039/d0ra00283f | DOI Listing |
Inorg Chem
October 2024
College of Chemistry and Chemical Engineering, Qingdao University, Qingdao 266071, Shandong, China.
Angew Chem Int Ed Engl
December 2024
Key Laboratory of Advanced Marine Materials, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, 315201, Ningbo, China.
Responsive photonic crystals (RPCs) exhibit dynamic chromism upon trigger by various solvents, showing potential applications in qualitative identification and quantitative analysis of multicomponent solvents. However, distinguishing similar solvents, especially traces of cosolvents, remains challenging due to the limited sensitivity of RPCs. To address this, we herein introduce brush-like polymeric gels inside photonic crystals, forming a brush-like polymeric photonic gel (BPPG) that can trace tiny component changes.
View Article and Find Full Text PDFACS Omega
February 2024
Division of Pharmaceutical Chemistry, Faculty of Pharmacy, Rhodes University, Makhanda 6139, South Africa.
Herein, we present a copper(II) metal-organic framework, () [(btec) = 1,2,4,5-benzenetetracarboxylate], that undergoes single-crystal-to-single-crystal transformations into two anhydrous phases and with the chemical formula , triggered by two-step dehydration at 403 and 433 K, respectively. After immersion in water for 3 days at room temperature, transformed into (), while both and took 1 week to revert to . Dynamic vapor sorption studies validated water-induced reversible structural transformations at 70% relative humidity (RH).
View Article and Find Full Text PDFThe dark-colored viologen radical cations are unstable in air and easily fade, thus greatly limiting their applications. If a suitable substituent is introduced into the structure, it will have the dual function of chromism and luminescence, which will broaden its application field. Here, Vio1·2Cl and Vio2·2Br were synthesized by introducing aromatic acetophenone and naphthophenone substituents into the viologen structure.
View Article and Find Full Text PDFInt J Biol Macromol
November 2022
Department of Biosciences and Bioengineering, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India. Electronic address:
According to current research, anti-cancer anthraquinones impact telomere disruption and may interact with G-quadruplex DNA that triggers signaling to apoptosis. The present study represents the biophysical investigation of oxidative stress, late apoptosis, and induced senescence among cancer cells after binding laboratory synthesized piperidine-based anthraquinone derivatives, 2, 6- Bis [(3-piperidino)acetamido)]anthracene-9,10-dione (N1P) and 2, 6-Bis [piperidino)propionamido]anthracene-9,10-dione (N2P), with G-quadruplex DNA. We employed biophysical approaches to explore the interaction of synthetic anthraquinone derivatives with quadruplex DNA sequences to influence biological activities in the presence of K and Na cations.
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