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The current research described in this paper, focuses on the development of a new quinoline-based Mannich-type benzoxazine and its use to obtain advanced carbonisation materials with a high energy storage capacity. Based on this, a quinoline-based benzoxazine monomer (Q-xda) was synthesised by a reaction between 8-hydroxyquinoline, xylylenediamine and paraformaldehyde, and it is characterised by FT-IR and H-NMR spectroscopy. Composites were prepared from the benzoxazine and variable weight percentages of graphitic carbon nitride (GCN) (, 5, 10, and 15 wt%). The oxazine ring-opening curing process of the polybenzoxazine composites, and its subsequent pyrolysis reaction was performed; and their chemical structures were confirmed using FT-IR spectroscopy. Also, the thermal and morphological characteristics of the composites were evaluated by XRD, thermogravimetric analysis (TGA), and SEM analyses. According to the results of the thermal experiments, adding GCN reinforcement significantly increased the thermal stability and char yield of the resultant composites. Electrochemical, and hydrophobic investigations were also carried out, and the results of these suggesting that the composites reinforced with 15 wt% GCN exhibit the highest dielectric constant (high = 10.2) and contact angle (145°). However, all the crosslinked composites demonstrated a remarkable electrochemical performance as pseudocapacitors. The resulting poly(Q-xda) + 15 wt% GCN electrodes showed a higher capacitance and a lower transferred charge resistance (, 370 F g at 6 A g and 20.8 Ω) than the poly(Q-xda) electrode (, 216 F g at 6 A g and 26.0 Ω). In addition, the poly(Q-xda) + 15% GCN exhibited a cycling efficiency of 96.2% even after 2000 cycles. From these results, it can be concluded that the constructed electrodes perform well in electrochemical operations.
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http://dx.doi.org/10.1039/d3sm01445b | DOI Listing |
Anal Chim Acta
October 2025
State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, China. Electronic address:
Background: The dynamic interplay between esterase activity and physicochemical microenvironments-such as polarity and viscosity-is critical for decoding early cellular dysfunction in processes like apoptosis, ferroptosis, and drug-induced toxicity. However, conventional probes typically report only a single parameter, obscuring interdependent changes in enzyme activity and membrane properties. This technological gap limits our ability to capture real-time, spatially resolved fluctuations within subcellular compartments.
View Article and Find Full Text PDFRSC Adv
August 2025
Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology Vellore 632016 India
Quinoline is a heterocyclic compound that plays a fundamental role in the study of chemical compounds, highlighting its importance in drug development. Its basic framework is crucial for synthesizing new pharmaceutical substances and facilitating the development of innovative drugs with significant therapeutic potential. A thorough examination of quinoline and its various derivatives, which exhibit a wide range of biological activities, greatly contributes to groundbreaking drug discoveries that can transform the medical industry.
View Article and Find Full Text PDFJ Med Chem
August 2025
Guangdong Provincial Key Laboratory of Chinese Medicine Ingredients and Gut Microbiomics, School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen 518060, China.
Both DNA methyltransferases (DNMTs) and histone deacetylases (HDACs) play complementary roles in epigenetic regulation, and their simultaneous inhibition is a promising strategy for cancer therapy. Herein, we report the design, synthesis, and biological evaluation of a series of quinoline-based hydroxamic acid derivatives as dual DNMT and HDAC inhibitors. Notably, compound emerged as the most potent dual-target inhibitor, with IC values of 365 and 0.
View Article and Find Full Text PDFSci Rep
August 2025
Basic Science Department, Delta University for Science and Technology, Mansoura, Egypt.
In pursuit of novel antimicrobial agents, a series of thiazolo[5,4-f]quinoline derivatives incorporating pyridine and thiophene moieties were synthesized and structurally characterized using IR and H-NMR spectroscopy. The synthetic strategy employed diverse condensation and cyclization reactions involving cyanoacetamide intermediates, aryl isothiocyanates, and α-halocarbonyl compounds. The resulting compounds were evaluated for their antimicrobial efficacy against Staphylococcus aureus, Escherichia coli, and Candida albicans.
View Article and Find Full Text PDFACS Chem Neurosci
September 2025
Metal Biochemistry and Oxidative Stress Laboratory, Center for Natural Sciences and Humanities, Federal University of ABC-UFABC, Santo André, São Paulo 09210-580, Brazil.
This study explores the potential of novel molecules that can act as copper chelators to treat Alzheimer's disease. Eight imines and one quinoline-based compound were synthesized, characterized, and evaluated as compounds that can act to reverse neurodegeneration in vivo. Their ability to extract copper from the Cu-β-amyloid complex, a key factor in Alzheimer's pathology, was assessed, achieving a remarkable in vitro activity for , , and .
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