Four selected quinone redox mediators with similar structure were conducted to accelerate reactive brilliant red K-2BP decolorization, and the accelerating structure-activity of redox mediators on the decolorization was also studied. Batch experiments were carried out to determine the catalyst effect on the decolorization of reactive brilliant red K-2BP with temperature of 35 degrees C and under anaerobic conditions. The experiment results suggested that (1) four similar chemical structure redox mediators [1, 4, 5, 8-Tetrachloroanthraquinone (1,4,5,8-AQ), Anthraquinone (AQ), 1,8-Dichloroanthraquinone (1,8-AQ), 1,5-Dichloroanthraquinone (1,5-AQ)], all accelerated the decolorization rate of reactive brilliant red K-2BP and the reaction rate was enhanced 1.4-3 times; (2) the accelerating order was 1,8-AQ >1 ,5-AQ > AQ >1,4,5,8-AQ at the quinone mediator concentration of 4 mmol x L(-1) and reactive brilliant red K-2BP concentration of 300 mg x L(-1); (3) under the reactive brilliant red K-2BP concentration of 300 mg x L(-1), 1,8-AQ had best accelerating effect, and the relationship between decoloring rate constants and 1,8-AQ concentration; (4) and the mediator acclerating effects also related to substituent positioning effects and conjugated effects. The structure-activity mathematical model of redox mediators was put forward, which could improve water-insoluble redox mediators catalytic strengthening theory system.
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Inorg Chem
January 2025
Department of Chemistry, The Johns Hopkins University, Baltimore, Maryland 21218, United States.
The hydrothermal synthesis of novel materials typically relies on both knowledge of the redox activities of all cations present in the reaction solution and a small toolset of so-called mineralizers to tune the solution's overall chemical potential. Upon the use of a less conventional mineralizer species, SiO, we show the stabilization of spiroffite-type CoTeO under less forceful hydrothermal conditions than those in previous reports. When synthesized in the presence of both SiO and each respective alkali carbonate as a secondary mineralizer, silicon substitution in place of tellurium in the host structure becomes apparent, and the corresponding disorder introduced gives rise to enhanced low-temperature ferromagnetism.
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January 2025
Jadavpur University, Chemistry, 188 Raja S. C. Mallick Road, 700032, Kolkata, INDIA.
Two π-radical complexes containing bisazo-aromatic-centered radical anion (1•-) were synthesized through in-situ electron transfer from metal-to-ligand using [IrI] and 2-(2-Pyridylazo)azobenzene (1) in inert hydrocarbon solvent. These are characterized as diradical [IrIII(1•-)2]+[2]+ and monoradical [IrIII(1•-)Cl2(PPh3)] 3. In contrast, a rare metal-mediated hydrolytic cleavage of the C(sp2)-N bond occurred in protic solvent resulting in quaternary radical complex [IrIII(1•-)(1')(PPh3)]+(4)+.
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Shanghai Key Lab of Chemical Assessment and Sustainability, School of Chemical Science and Engineering, Tongji University, Shanghai, 200092, People's Republic of China.
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Department of Physiology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, People's Republic of China.
Hypoxia ischemia (HI) is a leading cause of cerebral palsy and long-term neurological sequelae in infants. Given that mitochondrial dysfunction in neurons contributes to HI brain damage, this study aimed to investigate the regulatory role of miR-9-5p in mitochondrial function following HI injury. Overexpression of miR-9-5p in HI mice or HO-exposed PC12 cells suppressed neuronal injury, associated with increased mitochondrial copy number, normalizing mitochondrial membrane potential, improved nuclear factor-erythroid factor 2-related factor 2 (Nrf2) activation, and downregulation of Keap1.
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Northeastern University, Corrosion and Protection Center, NO. 3-11, Wenhua Road, Heping District, Shenyang, P. R. China, Shenyang, CHINA.
The dense passive film on 316L stainless steel is the key in its corrosion resistance. Its interactions with an electroactive biofilm are critical in deciphering microbial corrosion. Herein, an in-depth investigation using genetic manipulations and addition of an exogenous electron mediator found that extracellular electron transfer (EET) mediated by the electroactive S.
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