Silver,iron, and nickel immobilized on hydroxyapatite‐core‐shell γ‐Fe2O3 MNPs catalyzed one‐pot five‐component reactions for the synthesis of tetrahydropyridines by tandem condensation of amines,aldehydes, and methyl acetoacetate

In this study, Ag, Ni²⁺, and Fe²⁺ immobilized on hydroxyapatite‐core‐shell γ‐Fe₂O₃ nanoparticles (γ‐Fe₂O₃@HAp‐Ag, γ‐Fe₂O₃@HAp‐Ni²⁺, and γ‐Fe₂O₃@HAp‐Fe²⁺) as a new and reusable Lewis acid magnetic nanocatalyst was successfully synthesized and reported for an atom economic, extremely facile, and environmentally benign procedure for the synthesis of highly functionalized tetrahydropyridines derivatives 4a‐t is described by one‐pot five‐component reaction of 2 equiv of aldehydes 1 , 2 equiv of amines 2 , and 1 equiv of methyl acetoacetate 3 in EtOH at room temperature in good to high yields and short reaction time. The presented methodology offers several advantages such as easy work‐up procedure, reusability of the magnetic nanocatalyst, operational simplicity, green synthesis avoiding toxic reagents and solvent, mild reaction conditions, and no tedious column chromatographic separation.     

Cellulosic nanoparticles from alfa fibers (<Emphasis Type="Italic">Stipa tenacissima)</Emphasis>: extraction procedures and reinforcement potential in polymer nanocomposites

The microstructure and chemical composition of alfa (Stipa tenacissima) were investigated. The polysaccharide and lignin contents were around 70 and 20 wt%, respectively. From the bleached and delignified fibers, two types of nanosized cellulosic particles were extracted, namely cellulose nanocrystals and microfibrillated cellulose (MFC). The former correspond typically to the elementary crystallite units of the cellulose fibers, with a rod-like morphology and an aspect ratio of about 20. The latter, mechanically disintegrated from oxidized bleached fibres, presents an entangled fibrillar structure with widths in the range 5-20 nm. The reinforcing potential of the ensuing nanoparticles was investigated by casting a mixture of acrylic latex and aqueous dispersion of cellulose nanoparticles. Thermo-mechanical analysis revealed a huge enhancement of the stiffness above the glass transition of the matrix. Significant differences in the mechanical reinforcing capability of the nanoparticles were reported.     

Cyclotriphosphazene,a scaffold for 19F MRI contrast agents

A cyclotriphosphazene substituted with six 3,5-bis(trifluoromethyl) benzyloxy units was designed as a novel ¹⁹F MRI contrast agent. The resulting molecule has 36 magnetically equivalent fluorine atoms and exhibited suitable MRI properties with high imaging sensitivity, confirming the proof-of-concept as a convenient scaffold for the production of new ¹⁹F MRI contrasts agents.     

X-ray structure of palladium (II) complex and its catalytic activity on Suzuki–Miyaura reaction under mild conditions

Research on Chemical Intermediates - Palladium (II) complex with 4-tert-butylbenzoic hydrazide (TBBH)/triphenylphosphine (PPh3) ligands was successfully synthesized and characterized by X-ray,...     

Ab initio MRD-CI investigation of the electronic spectrum of 1-chloromethyl hypochlorite ClCH2OCl in comparison with isomeric dichloromethanol Cl2CHOH

The electronic absorption spectrum of 1-chloromethyl hypochlorite ClCH₂OCl is computed with multi-reference configuration interaction (MRD-CI) methods and compared to isomeric dichloromethanol. While the first dipole-allowed transitions of dichloromethanol Cl₂CHOH are obtained above 7 eV, the corresponding transitions of ClCH₂OCl are obtained at much lower energy, namely 3.66eV (1¹A″ ←[Xtilde]¹A′), 4.96eV (2¹A′←[Xtilde]¹A′), 6.04eV (2¹A″←[Xtilde]¹A′) and 6.67eV (3¹A′ ← [Xtilde]¹ A′). A further strong transition is computed at 7.82eV (4¹A′ ← [Xtilde]¹A′) with a relatively large oscillator strength of ? = 0.4.     

PHA-L lectin and carbohydrate relationship: conjugation with CdSe/CdS nanoparticles, radiolabeling and in vitro affinities on MCF-7 cells

This research aims to investigate the interaction between phytohemagglutinin-L (PHA-L) and sialic acid, which is abundant on the breast cancer cell (MCF-7) surface and displays monosaccharide characteristics, by experimental and computational methods. Experimentally, CdSe/CdS nanoparticles (QDs) were synthesized; PHA-L was conjugated with QDs and labeled with ¹²⁵I. Radiolabeling yield was found to be 97 ± 1.2 %. Afterwards, in vitro bioaffinities of radiolabeled PHA-L conjugated QDs have been investigated on MCF-7 cells and it has been observed that the cell incorporation increased with time. The results indicated that ¹²⁵I labeled QD-PHA-L conjugates represent significant affinity on MCF-7 cells. In the second step of the study, the crystal structure of carbohydrate interaction surface of PHA-L was extracted from the crystal structure of PHA-L. The interactions between this surface and sialic acid were calculated by computational tools. These calculations revealed specific interactions between PHA-L and sialic acid. Semi-empirical methods, PM3 and AM1, were used in these calculations. Significant outcomes have been obtained from the experimental and computational studies and these results demonstrated that PHA-L may be an effective agent for imagining MCF-7 cells.     

SPE and determination by FAAS of heavy metals using a new synthesized polymer resin in various water and dried vegetables samples

Firstly, poly[phenyl thiadiazole methacrylamide-co-divinylbenzene-co-2-acrylamido-2-methylpropane sulfonic acid] (PTMAAm-co-DVB-co-AMPS), a new polymer resin was synthesized. This polymer resin was characterized by elemental analyzer, X-ray diffractometer, scanning electron microscope (SEM) and IR spectrometer. The glass column packed with the synthesized polymer resin was used for solid phase extraction (SPE). At the same time, the analytes were separated and preconcentrated from various water, dried vegetables samples and standard reference material (CRM) with SPE and determined by flame atomic absorption spectrometer (FAAS). The experimental conditions of this method such as pH, flow rates of sample, flow rates of eluent, type / concentration / volume of eluent, sample volume and matrix ions were examined. The limits of detection (µg L^?1) were calculated (3s) 0.9 for Mn(II), 1.4 for Cd(II), Co(II) and Zn(II), 1.5 for Cr(III), 2.2. for Cu(II), 1.9 for Pb(II),1.5 for Ni(II) and 1.9 for Fe(III) (n = 21). The low relative standard deviation, ≤ 2% (n = 11) and preconcentration factor as 75 for analytes were obtained.     

On-line preconcentration and determination of Au(III) in various environmental/industrial samples by flame atomic absorption spectrometry

A rapid and simple on-line method is described for the determination of Au(III) in various samples. The method is based on the sorption of gold(III) on Lewatit MonoPlus TP207 chelating resin including the iminodiacetate group, which is used as sorbent material and packed in a minicolumn. The chemical variables such as the pH of the sample solution, eluent type, interfering ions and concentrations of reagents, and instrumental variables such as sample loading volume, reagents flow rates, and tubing length, which affect the efficiency of the method were studied and optimised. Au(III) was sorbed on the chelating resin, from which it could be eluted with 3 mol L^?1 HCl, and then introduced directly to the nebuliser-burner system of FAAS. The limit of detection of the method was 0.2 µg L^?1 while the relative standard deviation was <4.0% for 20 µg L^?1 Au(III) concentration. The preconcentration factor was found to be 106 while the optimised sample volume was 15.3 mL. The accuracy of the method was verified by analysing the certified reference material. The developed method was applied successfully for the determination of gold in different samples with satisfactory results.