Design, Synthesis, Characterization, Catalytic, Fluorometric Sensing, Antimicrobial and Antioxidant Activities of Schiff Base Ligand Capped AgNPs.

In recent days, the usage of biological and non-biological pollutants increased which poses a significant threat to environmental and biological systems. Therefore, the present aim is to develop effective methods to treat such pollutants by using highly stable and small-sized Schiff base ligand capped silver nanoparticles (AgNPs) with a face-centered cubic (fcc) crystalline structure and the size range is 5-10 nm. The potent role of the resulting synthesized AgNPs was found to be on multiple platforms such as catalyst, sensor, antioxidant, and antimicrobial disinfectant. The synthesized AgNPs were characterized through UV-vis spectroscopy, PL, FTIR, XRD, SEM, and TEM. The FTIR spectrum of AgNPs exhibited the interacted functional groups of Schiff base and size was estimated by XRD and TEM. AgNPs were able to catalytically degrade approximately 95% of methylene blue (MB), rhodamine B (RhB), and eosin Y (EY) dyes within 80 min of reaction time using NaBH4. The fluorometric sensor studies of synthesized AgNPs showed selective sensing of the potentially hazardous Fe2+ ion in water. As an antimicrobial agent, the AgNPs are effective against both Gram-positive and Gram-negative bacteria; as well as fungi, with the zones of clearance as approximately compatible with standard drugs. The AgNPs displayed a greater ability to scavenge free radicals, especially DPPH when compared with AgNPs and ascorbic acid. Thus, the results of this study validate the triple role of AgNPs derived via a simple synthesis as a catalyst, sensor, antioxidant, and antimicrobial agent for effective environmental remediation.

Ferroxidase-like and antibacterial activity of PtCu alloy nanoparticles.

Many metal nanoparticles are reported to have intrinsic enzyme-like activities and offer great potential in chemical and biomedical applications. In this study, PtCu alloy nanoparticles (NPs), synthesized through hydrothermal treatment of Cu2+ and Pt2+ in an aqueous solution, were evaluated for ferroxidase-like and antibacterial activity. Electron spin resonance (ESR) spectroscopy and colorimetric methods were used to demonstrate that PtCu NPs exhibited strong ferroxidase-like activity in a weakly acidic environment and that this activity was not affected by the presence of most other ions, except silver. Based on the color reaction of salicylic acid in the presence of Fe3+, we tested the ferroxidase-like activity of PtCu NPs to specifically detect Fe2+ in a solution of an oral iron supplement and compared these results with data acquired from atomic absorption spectroscopy and the phenanthroline colorimetric method. The results showed that the newly developed PtCu NPs detection method was equivalent to or better than the other two methods used for Fe2+ detection. The antibacterial experiments showed that PtCu NPs have strong antibacterial activity against Staphylococcus aureus and Escherichia coli. Herein, we demonstrate that the peroxidase-like activity of PtCu NPs can catalyze H2O2 and generate hydroxyl radicals, which may elucidate the antibacterial activity of the PtCu NPs against S. aureus and E. coli. These results showed that PtCu NPs exhibited both ferroxidase- and peroxidase-like activity and that they may serve as convenient and efficient NPs for the detection of Fe2+ and for antibacterial applications.

Fluorescent Carbon Dots for Sensitive and Rapid Monitoring of Intracellular Ferrous Ion.

Although iron is an essential constituent for almost all living organisms, iron dyshomeostasis at a cellular level may trigger oxidative stress and neuronal damage. Hence, there are numerous reported carbon dots (CDs) that have been synthesized and applied to determine intracellular iron ions. However, among reported CDs focused to detect Fe3+ ions, only a few CDs have been designed to specifically determine Fe2+ ions over Fe3+ ions for monitoring of intracellular Fe2+ ions. We have developed the nitrogen-doped CDs (NCDs) for fluorescence turn-off detection of Fe2+ at cellular level. The as-synthesized NCDs exhibit a strong blue fluorescence and low cytotoxicity, acting as fluorescence probes to detect Fe2+ as low as 0.702 µM in aqueous solution within 2 min and visualize intracellular Fe2+ in the concentration range from 0 to 500 µM within 20 min. The as-prepared NCDs possess some advantages such as high biocompatibility, strong fluorescence properties, selectivity, and rapidity for intracellular Fe2+ monitoring, making NCDs an excellent nanoprobe for biosensing of intracellular ferrous ions.

Mesopores silica nanotubes-based sensors for the highly selective and rapid detection of Fe2+ ions in wastewater, boiler system units and biological samples.

Mesopores silica nanotubes (MSNTs)-based chemical sensors for the rapid detection and of highly selective Fe2+ ions have been prepared. The novel nanosensors were prepared via immobilization of 1,10-phenanthroline-5-amine (PA) and bathophenanthroline (BP) onto the MSNTs. The resultant PA and BP sensors display high sensitivity for detection the Fe2+ ions in tap water, river water, sea water, two units in simple cycle power station, and biological samples. More interestingly, upon meeting ultra-trace amount of Fe2+ ions, a red complex appears at once. Color changes can be seen from the naked eye and tracked with a smartphone or spectrophotometric techniques. The response time that is necessary to achieve a stable signal was less than 15 s. The Univariate (Univar) calibration technique had been utilized for the determination of figures of merits. The detection limit obtained from the digital image analysis was 19 ppb (7.04 × 10-7 M) for Fe2+ ions, while the obtained from the spectrophotometric method was 6.7 ppb (2.48 × 10-7 M). Therefore, the two sensors had been successfully used in the determination of Fe2+ in several real samples with high sensitivity and selectivity. In addition, they can be used as a simple, rapid, and portable method to detect and quantify the pre rust in any cooler system.

Synthesis and Discovery of Schiff Base Bearing Furopyrimidinone for Selective Recognition of Zn2+ and its Applications in Cell Imaging and Detection of Cu2.

A simplefuro [2,3-d]pyrimidinone-based Schiff base FPS was synthesized via aza-Wittig reaction and structure elucidation was carried out by spectroscopic studies FT-IR, 1H NMR, and 13C NMR and mass spectrometry. FPS showed weak fluorescence emission in methanol and the selectivity of FPS to different metal ions (Mn2+, Ca2+, Fe2+, Fe3+, Mg2+, Al3+, Ba2+, Ag+, Co2+, Na+, K+, Cu2+, Zn2+, Pb2+, Bi3+) were studied by absorption and fluorescence titration. The results show that FPS has selective fluorescence sensing behavior for Zn2+ ions and the limit of detection (LOD) was calculated to be 1.19 × 10-8 mol/L. Moreover, FPS-Zn2+ acts as a metal based highly selective and sensitive new chemosensor for Cu2+ ions and the LOD was calculated to be 2.25 × 10-7 mol/L. In accordance with the results and theoretical calculations, we suspected that the binding mechanisms of FPS to Zn2+ and Cu2+ were assigned to be the cooperative interaction of Zn2+(Cu2+)-N.

A sensitive "Switch-on" phosphorescent probe for ferrous iron quantification in drug and In vitro imaging of living cells.

Iron plays an important role in various physiological processes. However, the detailed biological functions of iron have not been sufficiently explored because of a lack of effective methods to monitoring iron, especially the labile ferrous ion (Fe2+). In the current study, a novel turn-on phosphorescent probe for Fe2+ quantification and visualization has been proposed based on the hybrid nanocomposite of manganese dioxide and gemini iridium complex (MnO2-GM-Ir). The surfactant-like GM-Ir with positive charges was beneficial to combine with the negatively charged manganese dioxide (MnO2) nanosheets, and thus endowing the MnO2-GM-Ir nanocomposite excellent dispersion ability in the water as well as efficiently avoiding the interference to the detection caused by the agglomeration of nanocomposite. Phosphorescence of GM-Ir was effectively quenched by MnO2 nanosheets through fluorescence resonance energy transfer (FRET) and the inner filter effect (IFE), while the phosphorescence could be significantly recovered in the presence of Fe2+via a selective Fe2+-mediated reduction of MnO2 nanosheets, indicating a highly-specific selectivity towards Fe2+ with a low detection limit (80 nM). The drug test assay and in vitro imaging studies further proved that the MnO2-GM-Ir nanocomposite could be employed as a promising probe for the quantitative detection of exogenous Fe2+ in drug and in vitro imaging of living cells.

N-doped carbon dots/H2O2 chemiluminescence system for selective detection of Fe2+ ion in environmental samples.

The nitrogen doped carbon dots (N-CDs) produces strong chemiluminescence (CL)-emission due to hydroxyl radical (•OH) induced electron-hole transition in N-CDs. The Fe2+ has the ability to generate •OH from available hydrogen peroxide (H2O2). Therefore, a pre-mixed N-CDs/H2O2 solution was utilized for selective quantification of Fe2+ in solution via CL-emission. A linear increase in the CL-emission intensity was observed within increase in Fe2+ concentration. The N-CDs/H2O2 system enabled the detection of Fe2+ up to lower concentration of 0.2 × 10-9 M with a linear dynamic range of 1.0 × 10-9-1.0 × 10-6 M. Significantly, no CL-emission was observed when other divalent cations, Al3+, Fe3+, or Cr3+ were injected to this system. Moreover, no interference was observed when a mixed solution of Fe2+ and other cations were introduced to N-CDs/H2O2. The practical evaluation of N-CDs/H2O2 system was demonstrated for detection of Fe2+ in tap, lotus pond, and canal water samples. The easy detection, high sensitivity, and selectivity make this method a significant tool for analysis of Fe2+ in solution.

Cellulose-Based Sensor Containing Phenanthroline for the Highly Selective and Rapid Detection of Fe2+ Ions with Naked Eye and Fluorescent Dual Modes.

Iron ions play a vital role in many biological processes, and their concentrations are responsible for human health. Therefore, it is essential to detect the concentration of iron ions by a rapid, accurate, highly selective, and practical method. Herein, we have synthesized a cellulose-based fluorescent sensor (Phen-MDI-CA) for the highly selective and rapid detection of Fe2+ ions via chemically bonding 1,10-phenanthroline-5-amine (Phen) onto cellulose acetate (CA) using 4,4'-methylene diphenyl diisocyanate (MDI) as a cross-linker. Benefiting from the anchoring and diluting effect of a cellulose skeleton, the resultant Phen-MDI-CA displays excellent fluorescence properties in both solution and solid state. More interestingly, a cellulose-based polymer chain significantly improves the sensitivity of phenanthroline to Fe2+ ions. Upon meeting Fe2+ ions, a red, insoluble, and nonfluorescent Fe-(Phen-MDI-CA) complex appears immediately; thus, Phen-MDI-CA can work as a multimode chromogenic sensor for the highly selective, sensitive, and rapid detection of Fe2+ ions. In the instrument-free visual mode, the detection limit for Fe2+ ions is 50 ppb, and in fluorescence mode, the detection limit is 2.6 ppb. To our knowledge, this is the first time that such a low detection limit for Fe2+ ions in aqueous media has been observed by the naked eye. In addition, Phen-MDI-CA has good solubility and processability in common organic solvents, which facilitates its use in different material forms, e.g., printing ink, coating, and film. Therefore, the Fe2+-responsive and chromogenic Phen-MDI-CA exhibits a huge potential in the detection and extraction of Fe2+ ions.