Publications by authors named "Shaeel Ahmed Al-Thabaiti"

Bimetallic nanoparticles exhibit bifunctional or synergistic effects prevailing between two metals with the capabilities of enhanced electronic, catalytic, and optical properties. Green synthetic routes have gained tremendous interest because of the noninvolvement of toxic and harmful chemical reagents in preparation. Therefore, we develop bimetallic Ag-Cu nanoparticles (Ag-Cu NPs) through an eco-friendly and biocompatible preparation method.

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Electrochemically promoted transition metal-catalyzed C-H functionalization has emerged as a promising area of research over the last few decades. However, development in this field is still at an early stage compared to traditional functionalization reactions using chemical-based oxidizing agents. Recent reports have shown increased attention on electrochemically promoted metal-catalyzed C-H functionalization.

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The binding affinity of a drug with carrier proteins plays a major role in the distribution and administration of the drug within the body. Tizanidine (TND) is a muscle relaxant having antispasmodic and antispastic effects. Herein, we have studied the effect of tizanidine on serum albumins by spectroscopic techniques, such as absorption spectroscopic analysis, steady, state fluorescence, synchronous fluorescence, circular dichroism, and molecular docking.

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Chitosan capped MnO‑iridium nanoparticles supported on nanoceria (Ch-MnO-Ir/CeO) were fabricated by using combination of colloidal solution and metal displacement galvanic methods. The oxidative degradation of acid orange 7 in aqueous solution by activated persulfate with the as-prepared nanoparticles was studied. The resulting Ch-MnO-Ir/CeO with SO, 80 % degraded 70.

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Self aggregation, sorption, and interaction of Congo red, with cetyltrimethylammonium bromide (CTAB), sodium dodecylsulfate (SDS), Ag(+) ions and silver nanoparticles have been determined spectrophotometrically. Congo red self-aggregation was identified from UV-visible spectra due to the shrinkage in an absorption band at 495 nm. The shape of the absorbance spectrum changed entirely with increasing [Congo red] but wavelength maxima remain unchanged.

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The present study explores the reducing and capping potentials of aqueous Raphanus sativus root extract for the synthesis of silver nanomaterials for the first time in the absence and presence of two stabilizers, namely, water-soluble starch and cetyltrimethylammonium bromide (CTAB). The surface properties of silver nanoparticles (AgNPs) were determined by dynamic light scattering (DLS), transmission electron microscopy (TEM), energy dispersion X-ray spectroscopy (EDX), scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared (FT-IR) techniques. The mean size of AgNPs, ranging from 3.

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Biomimetic and economic method for the synthesis of silver nanoparticles (AgNPs) with controlled size has been reported in presence of shape-directing cetlytrimethylammonium bromide (CTAB). Biochemical reduction of Ag(+) ions in micellar solution with an aqueous lemon extract produced spherical and polyhedral AgNPs with size ranging from 15 to 30 nm. The influence of [CTAB] and [lemon extract] on the size of particles, fraction of metallic silver and their antimicrobial properties is discussed.

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In this paper we report the UV-visible and transmission electron microscopy (TEM) evidence to the formation of stable yellow-orange colored complex, which is attributed to the formation of ion-pair between sub-aggregates of cetyltrimethylammonium bromide (CTAB) and gold at room temperature. The position of wavelength maxima (λmax) and shape of the spectra strongly depends on the reaction conditions, i.e.

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Starch-capped copper nanoparticles (CuNPs) were prepared by a chemical reduction method using hydrazine, copper sulfate and starch as reducing, oxidizing and stabilizing agents, respectively, for the first time at room temperature. The products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), electron diffraction patterns (EDX), X-ray photoelectron spectroscopy (XPS), fourier transform infrared (FT-IR) spectroscopy, thermo-gravimetric analysis (TGA), and ultraviolet-visible spectroscopy. The effect of [starch], [hydrazine] and [copper sulfate] on the optical properties of CuNPs were studied by UV-visible spectrophotometrically.

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2-Phenyl-N,N'-bis(pyridin-4-ylcarbonyl)butanediamide ligand with a series of transition metal complexes has been synthesized via two routes: microwave irradiation and conventional heating method. Microwave irritation method happened to be the efficient and versatile route for the synthesis of these metal complexes. These complexes were found to have the general composition M(L)Cl2/M(L)(CH3COO)2 (where M = Cu(II), Co(II), Ni(II), and L = ligand).

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Silver nanocomposites (AgCPs) have been synthesized by chemical reduction from silver nitrate and sodium borohydride in presence of two stabilizers. Starch and poly (vinyl) alcohol, PVA with its rich source of polyhydroxy groups has been exploited for the capping of AgCPs. The ageing of NaBH4 aqueous solution, molar ratios of the reactants, nature of the stabilizers, mixing order of NaBH4 as well as capping agents have great influence on the morphology of AgCPs.

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A simple one-spot synthetic route for the production of Ag-nanoparticles using aqueous extract of citrus lemon is being reported in presence of shape-directing cetyltrimethylammonium bromide (CTAB). To our knowledge, this is the first report where the biomolecules form a layer around a group of the Ag-nanoparticles in which the inner layer is bound to the AgNPs surface via the hydroxyl groups of citric acid. The appearance of a sharp surface plasmon resonance band in the UV-visible region might be due to the formation of spherical Ag-nanoparticles.

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Azoles are generally fungistatic, and resistance to fluconazole is emerging in several fungal pathogens. In an attempt to find novel azole antifungal agents with improved activity, a series of tetrazole ring bearing acylhydrazone derivatives were synthesized and screened for their in vitro antifungal activity. The mechanism of their antifungal activity was assessed by studying their effect on the plasma membrane using flow cytometry and determination of the levels of ergosterol, a fungal-specific sterol.

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Silver nanoparticles were prepared by a simple chemical reduction method using ascorbic acid and starch as reducing and stabilizing agents, respectively. The effect of starch, silver ions and ascorbic acid was studied on the morphology of the silver nano-particles using UV-visible spectrophotometry. The initial reaction time min and amount of starch were important parameters for the growth of Ag-nanoparticles.

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We report a simple chemical reduction method for the synthesis of different colored silver nanoparticles, AgNP, using tyrosine as a reducing agent. Effects of cetyltrimethylammonium bromide, CTAB, and tyrosine concentrations are analyzed by UV-visible measurements and scanning electron microscopy (SEM) to evaluate the mode of AgNP aggregation. The position and shape of the surface resonance plasmon absorption bands strongly depend on the reaction conditions, i.

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Silver nanoparticles were prepared by the reduction of AgNO(3) with aniline in dilute aqueous solutions containing cetyltrimethlyammonium bromide, CTAB. Nanoparticles growth was assessed by UV-vis spectroscopy and the average particle size and the size distribution were determined from transmission electron microscopy, TEM. As the reaction proceeds, a typical plasmon absorption band at 390-450nm appears for the silver nanoparticles and the intensities increase with the time.

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In this paper, we describe a simple method for the synthesis of MnO(2) nanostructures (quantum dots) by permanganate oxidations of methionine and cysteine. Upon addition of permanganate to a solution of reductant (methionine and/or cysteine), yellow-brown color species appears within the time of mixing which was stable for several weeks. The UV-vis spectroscopy and transmission electron microscopy (TEM) techniques were used to characterize the nature of color formed.

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Silver nanoparticles were prepared in aqueous silver nitrate solution using hydrazine as reducing agents in presence of two ionic surfactants (cetyltrimethylammonium bromide; CTAB and sodium dodecyl sulfate; SDS) and one non-ionic surfactant (Triton X-100). The reaction rate was determined spectrophotometrically. The nature of the head group of these surfactants is responsible for the formation of stable, yellow and transparent silver sol.

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Kinetic data for the silver nitrate-ascorbic acid redox system in presence of three surfactants (cationic, anionic and nonionic) are reported. Conventional spectrophotometric method was used to monitor the formation of surfactant stabilized nanosize silver particles during the reduction of silver nitrate by ascorbic acid. The size of the particles was determined with the help of transmission electron microscope.

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