New ciprofloxacin–dithiocarbamate–benzyl hybrids: design,synthesis, antibacterial evaluation,and molecular modeling studies

Research on Chemical Intermediates - We designed and synthesized a series of new ciprofloxacin–dithiocarbamate–benzyl hybrids 5a–n as potential antibacterial agents. All of the...     

Two‐stage phase separation of cellulose acetate membranes modified with plasma‐treated natural zeolite: Response surface modeling

Cellulose acetate (CA) microfiltration membranes were prepared by two‐stage vapor‐induced phase separation (VIPS) and immersion precipitation. To improve the hydrophilicity and permeability of the membranes at low operating pressures, plasma‐treated natural zeolite was incorporated into the membranes. A response surface methodology based on the three‐level central composite design (CCD) was used to model and optimize the casting solution composition of the membranes with the aim of maximizing membranes permeability. Three independent variables for CCD optimization were concentration of CA, polyvinylpyrrolidone (PVP) pore former, and plasma‐treated zeolite additive. The results showed that a second‐order polynomial model could properly predict the response (pure water flux) at any input variable values with a satisfying determination coefficient (R²) of 0.954. Also, analysis of variance (ANOVA) confirmed the adequacy of the obtained model. The permeability of the prepared membranes increased by increasing zeolite loading from 0.10 to 0.50 wt%, which was related to the membranes morphology and porosity and confirmed by scanning electron microscopy (SEM) images. Pure water flux of the membranes decreased by increasing CA concentration while an optimum PVP amount was required to reach the maximum flux. The result of the bubble point analysis well matched with surface SEM images of the membranes and permeability trend predicted by CCD model. Also, the prepared CA membranes with different compositions showed no toxicity for mouse L929 fibroblast, which indicated their nontoxic and biocompatible nature.     

Characterization of hydrogels formed by non-toxic chemical cross-linking of mixed nanofibrillated/heat-denatured whey proteins

In the current research, whey protein isolate (WPI) solution was nanofibrillated or denatured by heating at pH 2.0 or 8.0, respectively. The formation of whey protein nanofibrils with a nanometric thickness and micrometric length was confirmed by atomic force microscopy. Subsequently, different concentrations of citric acid (0–200 mM) as a gelling agent was used to fabricate cold-set hydrogels from heat-denatured, fibrillated, and mixed fibrillated/heat-denatured protein solutions at pH value of 8.0. The fibrillated and mixed fibrillated/heat-denatured solutions required lower concentrations of citric acid to form self-supporting gels compared to the heat-denatured WPI. The formation of covalent bonds between the network-building protein units through the citric acid-induced gelation was confirmed by gel electrophoresis and Fourier transform infrared spectroscopy. Hydrogels made of nanofibrillated and mixed solutions were firmer, had a lower water holding capacity, and showed more degradation at the simulated gastric fluid than the gel from heat-denatured WPI. The increase in citric acid concentration also increased the firmness and gastric degradation stability of the hydrogel samples. The results also showed that the hydrogels in the presence of nanofibrils were degraded much more than the fibril-free gel samples in the simulated gastric condition. Generally, these findings suggested that the combination of nanofibrillation and citric acid-mediated cross-linking could be employed to fabricate hydrogels with excellent techno-functional attributes.

     

Ligand‐free,copper‐catalyzed,one‐pot,three‐component synthesis of novel 1,2,3‐triazole‐linked indoles in magnetized water

Magnetized water (MW) is used as a green and new solvent‐promoting medium for the one‐pot, three‐component synthesis of novel 1,2,3‐triazole‐linked indoles catalyzed by copper iodide. A broad range of 2‐aryl‐1‐(prop‐2‐ynyl)‐1H‐indole‐3‐carbaldehydes were reacted with alkyl halides and sodium azide via copper‐catalyzed azide–alkyne cycloaddition reactions in MW in the absence of any ligand. This method offers the advantages of short reaction times, green procedure, low cost, simple work‐up, quantitative reaction yields, and no need for any organic solvent.     

Particle size dependence of electro-optical switching in ZrP nano colloid

Aqueous colloid of 2-dimensional (2D) α-ZrP nanoparticles can serve as an excellent material for Kerr devices. We investigate the influence of the particle size on the electro-optical switching for isotropic and biphasic α-ZrP colloids that exhibit stable Kerr effect. Smaller sized α-ZrP colloid has wider range of isotropic and biphasic phases, but since the anisotropic polarizability is approximately proportional to square diameter of particles, the larger sized α-ZrP colloid has higher birefringence at a given concentration. The dynamic response time is also dramatically influenced by the particle size. Smaller sized particle has lower viscosity, and the fall time monotonically increases with increasing particle size. However, the rise time has the minimum at around 0.6 μm owing to the competitive contributions of the anisotropic polarizability and the rotational viscosity. Thus, the particle size in α-ZrP colloid is an important factor to determine the electro-optical performance of a Kerr device based on 2D α-ZrP colloids. These findings will be important in developing electro-optical devices using lyotropic liquid crystal colloids.     

Towards the higher solubility and thermal stability of poly(aniline-<Emphasis Type="Italic">co</Emphasis>-<Emphasis Type="Italic">m</Emphasis>-bromoaniline)

In the current study, we have described the synthesis and the physical properties of poly(aniline-co-m-bromoaniline) conducting copolymers. The copolymers of different composition are essentially obtained by varying the molar feed ratio of the two monomers. The higher solubility of the copolymers could be procured as compared to polyaniline (PA) in different solvents. The electrical conductivity has been studied by two-probe method; at room temperature, the conductivity of the copolymer decreases upon increasing the molar ratio of m-bromoaniline monomer. The introduction of bromine (–Br) group reduces the degree of conjugation in the polymer chain. Thus, conduction of electrons is prohibited along the conjugated system. In the thermogravimetric analysis (TGA), a three-stage decomposition of the copolymer has been observed. The copolymers of poly(aniline-co-m-bromoaniline) are thermally stable at high temperature. The composition of the copolymer has been confirmed from the binding energies of C–C, C–N, and C–Br in the XPS study.     

Intensity modulated silver coated glass optical fiber refractive index sensor

Miniature optical fiber sensors with thin films as sensitive elements could open new fields for optical fiber sensor applications. Thin films work as sensitive elements and a transducer to get response and feedback from environments, in which optical fibers act as a signal carrier. A novel Ag coated intensity modulated optical fiber sensor based on refractive index changes using IR and UV-Vis(UV-visible) light sources is proposed. The sensor with an IR light source has higher sensitivity compared to a UV-Vis source. When the refractive index is enhanced to 1.38, the normalized intensity of IR and UV-Vis light diminishes to 0.2 and 0.8, respectively.