Crystal structure of (E)-1-{[(3,5-dimethylphenyl)imino]methyl}naphthalen-2-ol

This is an open-access article distributed under the terms of the Creative Commons Attribution Licence.The title compound, C19H17NO, has an E conformation about the N=C bond. The mol­ecule is relatively planar, with the benzene ring and naphthalene ring plane being inclined to one another by 4.28 (10)°. There is an intra­molecular O—H⋯N hydrogen bond generating an S(6) ring motif. In the crystal, mol­ecules are linked via C—H⋯O hydrogen bonds, forming chains propagating along [100]. Within the chains there are π–π inter­actions involving the benzene ring and the naphthalene ring system of an adjacent mol­ecule [inter-centroid distance = 3.6405 (14) Å].We thank the Spanish Ministerio de Economía y Competitividad (MAT2013-40950-R and FPI grants: BES-2011-046948 to author MSMA) and the ERDF for financial support.Peer Reviewe

Nano Sized Moringa oleifera an Effective Strategy for Pb(II) ions Removal from Aqueous Solution

Nano-sized  Moringa oleifera is considered an effective   biosorbent  with  high surface area from agricultural waste, low coast and environment-friendly which can be used for removal of  Pb2+ from waste water. Thus our study stem to investigate the ability of natural nano-sized biosorbents for removing  very toxic Pb2+ ions from aqueous solution. The investigated biosorbent (Moringa oleifera) was characterized by FTIR, SEM, TEM, XRD and EDX techniques. Moreover, the influence of pH, temperature, adsorbent dosage, contact time and initial metal ion concentration on adsorption process were investigated. The maximum biosorption capacities (qm) of Pb2+ ions by Moringa oleifera was 37.9 mg/g. The lowest biosorption was observed (61.4%) for Pb2+ ions at pH 2.0 while the highest one (94.36%) at pH 5. The optimum contact time for the adsorption process was found to be at 60 minutes. The amount of Pb2+ ions adsorbed increases with increasing in initial metal ion concentration. Moreover, biosorption capacity (qe) and removal efficiency of Pb2+ ions solutions increase as temperature increases. FT-IR data indicated that the adsorption of metal ions occurs on the surface of Moringa oleifera powder as the main functional groups that are responsible for metal ions binding are involved in the process. Furthermore, Thermodynamic studies confirmed that the biosorption process was endothermic and the positive value of ΔG° is quite common when an ion-exchan­­ge mechanism applies in the biosorption. The Positive value of ΔS◦ suggested an increase in randomness during the biosorption. The kinetics study of sorption indicates that the pseudo second-order model provides better correlation of the sorption data (R2=0.99) than the pseudo first-order model (R2 = 0.91), confirming the chemisorption of metal ions solutions on Moringa oleifera. The Freundlich isotherm has agood fit with the experimental data (R2 close to 1) compared to Langmuir isotherm (R2=0.99). This study shows that Moringa oleifera are available, low cost, effective and environment friendlly biosorbent for the removal of Pb2+ ions from aqueous environment. Keywords: Lead, biosorption, Thermodynamics, kinetics, removal efficiency, Moringa oleifera, isother

Kinetic investigation of hydroxide ion and DNA attack on some high spin iron (II) chelates Bearing ONO Donors amino acid Schiff bases

The reactivity of few novel high spin Fe(II) complexes of Schiff base ligands derived from 2-hydroxynaphthaldehyde and some variety of amino acids with OH- ion has been examined in aqueous mixture at temperature in the range 10–40 Co. Based on the kinetic investigations, the rate law and a plausible mechanism were proposed and discussed. The general rate equation was suggested as follows: rate = kobs [Complex], where kobs.= k1 + k2 [OH-]. Base catalyzed hydrolysis kinetics measurements imply pseudo-first order doubly stage rates due the presence of merand fac-isomers. The observed rate constants kobs are correlated the effect of substituent R in the structure of the ligands. From the effect of temperature on the rate; various thermodynamic parameters have been evaluated. The evaluated rate constants and activation parameters are in a good agreement with the stability constants of the investigated complexes

Enhancement of Exchange Bias and Perpendicular Magnetic Anisotropy in CoO/Co Multilayer Thin Films by Tuning the Alumina Template Nanohole Size

The interest in magnetic nanostructures exhibiting perpendicular magnetic anisotropy and exchange bias (EB) effect has increased in recent years owing to their applications in a new generation of spintronic devices that combine several functionalities. We present a nanofabrication process used to induce a significant out-of-plane component of the magnetic easy axis and EB. In this study, 30 nm thick CoO/Co multilayers were deposited on nanostructured alumina templates with a broad range of pore diameters, 34 nm ≤ Dp ≤ 96 nm, maintaining the hexagonal lattice parameter at 107 nm. Increase of the exchange bias field (HEB) and the coercivity (HC) (12 times and 27 times, respectively) was observed in the nanostructured films compared to the non-patterned film. The marked dependence of HEB and HC with antidot hole diameters pinpoints an in-plane to out-of-plane changeover of the magnetic anisotropy at a nanohole diameter of ∼75 nm. Micromagnetic simulation shows the existence of antiferromagnetic layers that generate an exceptional magnetic configuration around the holes, named as antivortex-state. This configuration induces extra high-energy superdomain walls for edge-to-edge distance >27 nm and high-energy stripe magnetic domains below 27 nm, which could play an important role in the change of the magnetic easy axis towards the perpendicular directionEl interés por las nanoestructuras magnéticas que exhiben anisotropía magnética perpendicular y efecto de sesgo de intercambio (EB) ha aumentado en los últimos años debido a sus aplicaciones en una nueva generación de dispositivos espintrónicos que combinan varias funcionalidades. Presentamos un proceso de nanofabricación utilizado para inducir una componente significativa fuera del plano del eje magnético fácil y del EB. En este estudio, se depositaron multicapas de CoO/Co de 30 nm de espesor sobre plantillas de alúmina nanoestructurada con un amplio rango de diámetros de poro, 34 nm ≤ Dp ≤ 96 nm, manteniendo el parámetro de red hexagonal en 107 nm. Se observó un aumento del campo de polarización de intercambio (HEB) y de la coercitividad (HC) (12 veces y 27 veces, respectivamente) en las películas nanoestructuradas en comparación con la película sin patrón. La marcada dependencia de HEB y HC con los diámetros de los agujeros antidotados señala un cambio de la anisotropía magnética de dentro a fuera del plano a un diámetro de nanoagujero de ∼75 nm. La simulación micromagnética muestra la existencia de capas antiferromagnéticas que generan una configuración magnética excepcional alrededor de los agujeros, denominada estado de antivórtice. Esta configuración induce paredes de superdominio extra de alta energía para la distancia de borde a borde >27 nm y dominios magnéticos de franja de alta energía por debajo de 27 nm, que podrían desempeñar un papel importante en el cambio del eje magnético fácil hacia la dirección perpendicula

A review on versatile applications of transition metal complexes incorporating Schiff bases

Schiff bases and their complexes are versatile compounds synthesized from the condensation of an amino compound with carbonyl compounds and widely used for industrial purposes and also exhibit a broad range of biological activities including antifungal, antibacterial, antimalarial, antiproliferative, anti-inflammatory, antiviral, and antipyretic properties. Many Schiff base complexes show excellent catalytic activity in various reactions and in the presence of moisture. Over the past few years, there have been many reports on their applications in homogeneous and heterogeneous catalysis. The high thermal and moisture stabilities of many Schiff base complexes were useful attributes for their application as catalysts in reactions involving at high temperatures. The activity is usually increased by complexation therefore to understand the properties of both ligands and metal can lead to the synthesis of highly active compounds. The influence of certain metals on the biological activity of these compounds and their intrinsic chemical interest as multidentate ligands has prompted a considerable increase in the study of their coordination behaviour. Development of a new chemotherapeutic Schiff bases and their metal complexes is now attracting the attention of medicinal chemists. This review compiles examples of the most promising applied Schiff bases and their complexes in different areas

Development and functionalization of magnetic nanoparticles as powerful and green catalysts for organic synthesis

Magnetic nanoparticles are a highly worthy reactant for the correlation of homogeneous inorganic and organic containing catalysts. This review deals with the very recent main advances in the development of various nano catalytic systems by the immobilization of homogeneous catalysts onto magnetic nanoparticles. Catalytic fields include the use of mainly cobalt, nickel, copper, and zinc ferrites, as well as their mixed-metal combinations with Cr, Cd, Mn and sometimes some lanthanides. The ferrite nanomaterials are obtained mainly by co-precipitation and hydrothermal methods, sometimes by the sonochemical technique, micro emulsion and flame spray synthesis route. Catalytic processes with application of ferrite nanoparticles include degradation (in particular photocatalytic), reactions of dehydrogenation, oxidation, alkylation, C–C coupling, among other processes. Ferrite nano catalysts can be easily recovered from reaction systems and reused up to several runs almost without loss of catalytic activity. Finally, we draw conclusions and present a futurity outlook for the further development of new catalytic systems which are immobilized onto magnetic nanoparticles

Kinetic investigation of hydroxide ion and DNA attack on some high spin iron (II) chelates Bearing ONO Donors amino acid Schiff bases

The reactivity of few novel high spin Fe(II) complexes of Schiff base ligands derived from 2-hydroxynaphthaldehyde and some variety of amino acids with OH- ion has been examined in aqueous mixture at temperature in the range 10–40 Co. Based on the kinetic investigations, the rate law and a plausible mechanism were proposed and discussed. The general rate equation was suggested as follows: rate = kobs [Complex], where kobs.= k1 + k2 [OH-]. Base catalyzed hydrolysis kinetics measurements imply pseudo-first-order doubly stage rates due the presence of merandfac-isomers. The observed rate constants kobs are correlated the effect of substituent R in the structure of the ligands.From the effect of temperature on the rate; various thermodynamic parameters have been evaluated. The evaluated rate constants and activation parameters are in a good agreement with the stability constants of the investigated complexes.Keywords: Base catalyzed hydrolysis, Isomer, Reaction mechanism, Thermodynamic parameters

Temperature and salt effects of the kinetic reactions of substituted 2-pyridylmethylene-8-quinolyl iron (II) complexes as antimicrobial, anti-cancer and antioxidant agents with Cyanide ions

Kinetics of substitution reaction of three high spin pyridylmethylene-8-quinolyl iron (II) complexes by CN- ions are studied spectophotometrically in various ratios of aqueous-methanol binary mixtures at 298 0.2 K. Kinetics of the substitution reaction follow the rate law (k2[CN−][complex])on applying of the conditions of the pseudo-first-order. Reactivity of the reaction was investigated in terms of organic ligand moiety and solvent effects. The rate of the reaction increases with increasing of the co-solvent, methanol ratio. This reactivity trend is predominantly due to increasing of the activity coefficient of those hydrophobic complexes in the organic methanol co-solvent depending upon the hydrophobicity of the substituent groups (R) in the coordinated ligand in the complexes. Moreover, reactivity trends of the prepared complexes in the presence of the inserted hydrophobic salts (TBAB, TEAB and TMAB) or hydrophilic salt (KBr) were studied. The observed decrease in the rate constants with increasing salt concentration is due to the cationic character of the reacting complexes. Furthermore, the synthesized complexes exhibited enhanced activity against selected strains of microbes. The ligands and their Fe(II) complexes were screened for anticancer activities against several cell lines of cancer. Furthermore, the antioxidant potential of the presented compounds was studied by applying DPPH assays and showed a potential activity compared with standard Vitamin C. The excellent antimicrobial and anticancer activities of the investigated Fe(II) chelates compared with literature could be promised to be pharmaceutical agents after further studies.The accepted manuscript in pdf format is listed with the files at the bottom of this page. The presentation of the authors' names and (or) special characters in the title of the manuscript may differ slightly between what is listed on this page and what is listed in the pdf file of the accepted manuscript; that in the pdf file of the accepted manuscript is what was submitted by the author

Impact of Co2+ substitution on microstructural evolution and magnetic properties of zinc ferrite nanoparticles synthesized by precipitation and hydrothermal-joint method

Resumen del póster presentado al 25th Congress of the International Union of Crystallography (IUCr), celebrado en Praga (Rep. Checa) del 14 al 22 de agosto de 2021.The microstructural characterization of spinel-ferrites has been long discussed in the literature. Such interests are justified by the spinel-ferrites potential applications that involve spintronic and magnetic resonance imaging (MRI), gas sensors, magnetic recording, medical diagnostics, antibacterial agents and self-controlled magnetic hyperthermia. In the present work, we have synthesized CoxZn1-xFe2O4 spinel ferrite nanoparticles (x= 0, 0.1, 0.2, 0.3 and 0.4) via the precipitation and hydrothermal-joint method. Structural parameters were cross-verified using Xray diffraction (XRD) and electron microscopy based-techniques. The magnetic parameters were determined by means of vibrating sample magnetometry. The as-synthesized CoxZn1-xFe2O4 nanoparticles exhibit high phase purity with a single-phase cubic spinel-type structure of Znferrite. The microstructural parameters of the samples were estimated by XRD line profile analysis using Williamson-Hall method. The calculated crystallite sizes from XRD analysis for the synthesized samples ranged from 8.3 to 11.4 nm. The electron microscopy analysis revealed that all powder samples are composed of regular spherical nanoparticles with highly homogeneous elemental composition. The CoxZn1-xFe2O4 spinel ferrite system exhibits paramagnetic, superparamagnetic and weak ferromagnetic behavior at room temperature depending on the Co2+ doping ratio, while ferromagnetic ordering with a clear hysteresis loop is observed at low temperature (5K). We concluded that the substitution of Zn with Co2+ ions impact both structural and magnetic properties of ZnFe2O4 nanoparticles.Spanish MINECO (MAT2016–78155-C2–1-R) and Gobierno del Principado de Asturias (GRUPIN-IDI/2018/0 0 0170) are acknowledged for the financial support.Peer reviewe