Metal Ion Complexes Research Articles

Synthesis, Characterization and Antioxidant Study of Some Metal Ion Complexes with Azo 1-(2,4,6-trihydroxy-3-((3-hydroxyphenyl) diazenyl) phenyl) Ethan-1-one.

اثناء تفاعل الديزنة تكونت صبغة أزو جديدة عن طريق تفاعل 3-امينوفينول مع 2,4,6-ثلاثي هيدروكسي اسيتوفينون . ثم تم تفاعل هذا الليكاند مع بعض ايونات العناصر الكروم والحديد الروديوم والروثينيوم بتكفؤهم الثلاثي والكوبلت الثنائي والموليبدينوم سداسي التكافؤ مكونة معقدات فلزية مختلفة بأشكال هندسية متعددة. تم ملاحظة تناسق مجموعة الازو مع ايونات العناصر من خلال ملاحظة ظهور حزم امتصاص الفلز مع النتروجين والاوكسجين بتقنية مطيافية الاشعة تحت الحمراءمشيرة إلى ارتباط النيتروجين والأكسجين مباشرة مع الفلز .تم تعيين الاوزان الجزيئية لليكاند ومعقداته بأستخدام مطيافية الكتلة وكذلك تم عمل تحليل للعناصر. تم قياس حزم امتصاص الاطياف الالكترونية لتحديد الشكل الهندسي للمعقدات , اضافة الى ذلك تم تحديد استقرارية المركبات من حيث احتواءها على جزيئات الماء من عدمه باستخدام تقنيتي المسح الحراري التفاضلي التحليل الحراري الوزني تم قياس تأثير المعقدات كمضادات اكسدة اتجاه 2,2-داي فينل بكريل هيدرازيل (DPPH) وهو عبارة عن جذر حر مستقر الذي يتم استخدامه لمعرفة فعالية كسح الجذور الحرة لنواع الاوكسجين النشطة ولوحظ التالي (H4L > Ascorbic acid > Mo-Complex > Fe-Complex > Cr-Complex > Rh-Complex > Ru-Complex) خلال ثلاثون دقيقة . اختبار DPPH قام باختزال الالكترون المنفرد لذرة النتروجين عن طريق استلام ذرة هيدروجين من المعقدات المضادة للكسدة لتكوين الهيدرازين المقابل . نتيجة الفحص تراوحت مابين قيم تثبيط لمركبات نشطة وغير نشطة تم ادراجها في البحث.

Synthesis, Characterization and Evaluation of the Antimicrobial and Herbicidal Activities of Some Transition Metal Ions Complexes with the Tranexamic Acid.

New tranexamic acid (TXA) complexes of ferric(III), cobalt(II), nickel(II), copper(II) and zirconium(IV) were synthesized and characterized by elemental analysis (CHN), conductimetric (Λ), magnetic susceptibility investigations (μeff), Fourier transform infrared (FT-IR), proton nuclear magnetic resonance (1H-NMR), ultraviolet visible (UV-vis.), optical band gap energy (Eg) and thermal studies (TG/DTG and DTA). TXA complexes were established in 1 : 2 (metal: ligand) stoichiometric ratio according to CHN data. Based on FT-IR and 1H-NMR data the disappeared of the carboxylic proton supported the deprotonating of TXA and linked to metal ions via the carboxylate group's oxygen atom as a bidentate ligand. UV-visible spectra and magnetic moment demonstrated that all chelates have geometric octahedral structures. Eg values indicated that our complexes are more electro conductive. DTA revealed presence of water molecules in inner and outer spheres of the complexes. DTA results showed that endothermic and exothermic peaks were identified in the degradation mechanisms. The ligand and metal complexes were investigated for their antimicrobial and herbicidal efficacy. The Co(II) and Ni(II) complexes showed antimicrobial activity against some tested species. The obtained results showed a promising herbicidal effect of TXA ligand and its metal complexes particularly copper and zirconium against the three tested plants.

Novel schiff base-azide metal complexes: Synthesis, spectral, nonlinear optics, and DFT studies

In order to enhance nonlinear optics (NLO)-based technologies, current research focuses on the design and synthesis of coordination materials. In this context, to investigate spectral and theoretical linear optical (LO)/nonlinear optical (NLO) behaviors, novel metal complexes including azide {[Mn (L1)2(N3)2], (9), [Ni(L1)2(N3)], (10), [Co2(L1)2(N3)2]⋅2H2O, (11); L1: N-(pyridin-2-ylmethylene)methanamine} were synthesized. The vibrational and electronic spectral features of complexes 9–11 were investigated by UV–Vis and FT–IR spectra. Depending on the central metal ion and coordination geometries of complexes, the microscopic static nonlinear behaviors were examined by using the CAM-B3LYP/and ωB97XD/6–311 + G (d,p)//LanL2DZ levels of density functional theory (DFT). Furthermore, the vibrational and electronic properties of complexes 9–11 based on the same levels of time-dependent/density functional theory (TD-DFT/DFT) were surveyed. Additionally, the theoretical χ(1), χ(2), and χ(3) parameters, known as linear optical, second-, and third-order nonlinear optical susceptibility tensors, as well as linear, second-, and third-order polarization parameters (P(1), P(2), and P(3)) for complexes 9–11 were examined. The greatest <β(0; 0,0)> value for complex 10 found to be 262.55 × 10−30 esu using CAM-B3LYP level is 820.5 and 2019.6 times higher than the urea findings (0.32 × 10−30 esu and 0.130 × 10−30 esu). The <γ(0; 0,0,0)> results indicate that complex 9 having the highest value obtained at 2216.40 × 10−36 esu using CAM-B3LYP level is 47.76 and 316.63 times greater than those of pNA (15 × 10−36 esu) and urea (7 × 10−36 esu), respectively. Complexes 10 and 9 demonstrated promising microscopic second-order and third-order NLO features, respectively. Our research is anticipated to provide insight into NLO materials that may have applications in optoelectronics and telecommunication field.

Electrochemiluminescence of a First-Row d6 Transition Metal Complex.

We report the electrochemiluminescence (ECL) of a 3d6 Cr(0) complex ([Cr(LMes)3]; λem=735 nm) with comparable photophysical properties to those of ECL-active complexes of 4d6 or 5d6 precious metal ions. The electrochemical potentials of [Cr(LMes)3] are more negative than those of [Ir(ppy)3] and render the [Cr(LMes)3]* excited state inaccessible through conventional co-reactant ECL with tri-n-propylamine or oxalate. ECL can be obtained, however, through the annihilation route in which potentials sufficient to oxidise and reduce the luminophore are alternately applied. When combined with [Ir(ppy)3] (λem=520 nm), the annihilation ECL of [Cr(LMes)3] was greatly enhanced whereas that of [Ir(ppy)3] was diminished. Under appropriate conditions, the relative intensities of the two spectrally distinct emissions can be controlled through the applied potentials. From this starting point for ECL with 3d6 metal complexes, we discuss some directions for future development.

Electrochemiluminescence of a First‐Row d6 Transition Metal Complex

AbstractWe report the electrochemiluminescence (ECL) of a 3d6 Cr(0) complex ([Cr(LMes)3]; λem=735 nm) with comparable photophysical properties to those of ECL‐active complexes of 4d6 or 5d6 precious metal ions. The electrochemical potentials of [Cr(LMes)3] are more negative than those of [Ir(ppy)3] and render the [Cr(LMes)3]* excited state inaccessible through conventional co‐reactant ECL with tri‐n‐propylamine or oxalate. ECL can be obtained, however, through the annihilation route in which potentials sufficient to oxidise and reduce the luminophore are alternately applied. When combined with [Ir(ppy)3] (λem=520 nm), the annihilation ECL of [Cr(LMes)3] was greatly enhanced whereas that of [Ir(ppy)3] was diminished. Under appropriate conditions, the relative intensities of the two spectrally distinct emissions can be controlled through the applied potentials. From this starting point for ECL with 3d6 metal complexes, we discuss some directions for future development.

A novel PVI-PVA/PS composite membrane modified by metal ions for CO2 separation: Effect and mechanism

The membrane process is potentially more energy-efficient than conventional separation technologies in the separation of carbon dioxide (CO2) /nitrogen (N2) from flue gas. In this work, a series of PVI (Polyvinylimidazole)-PVA (Polyvinyl alcohol) /PS (Polysulfone) membranes were prepared by co-blending two polymers, PVI and PVA, as the separation layer of the fixed carrier composite membrane. The separation performance increased by the dual action of PVA and the imidazole group in the PVI. Furthermore, Mg2+-PVI-PVA/PS and Cu2+-PVI-PVA/PS composite membranes were developed by adding Mg2+ and Cu2+, and the separation performance was considerably improved by complexing metal ions with PVA and PVI. Especially, Mg2+-PVI-PVA/PS demonstrated superior separation performance, with a CO2 permeation rate of 12 GPU and a CO2/N2 separation factor of 183 at a pressure of 1 bar. What’s more, the mechanism study clarified that the prepared composite membrane mainly relies on the facilitated transfer mechanism to achieve the selective separation of CO2. The presence of water molecules significantly improved the CO2 permeability and separation selectivity, indicating that PVI-PVA and Mg2+ could promote the hydration reaction of CO2 and H2O, forming easily mobile HCO3- carriers.

Construction of multilayer carbon magnetic heterostructures on the surface of carbon fibers to improve the absorption performance

AbstractThis study utilizes the strong complexation effect of polydopamine on metal ions and constructs multilayer carbon magnetic heterostructures on the surface of carbon fibers through the in situ reduction method, thereby obtaining a new type of multilayer carbon‐based composite absorbing material. The absorption properties at different layers were analyzed and compared through various characterization methods. Finally, the double‐layer structure demonstrated outstanding electromagnetic wave absorption characteristics, exhibiting a wide effective absorption bandwidth of 7.24 GHz and robust absorption of −44.48 dB, all within a mere thickness of 3.5 mm. Therefore, excellent market prospects for this material are anticipated.Highlights A multilayer carbon magnetic heterostructure absorbing material was constructed on micrometer‐scale carbon fibers. The test results show that a wide effective absorbing bandwidth of 7.24 GHz and a minimum reflection loss of −44.48 dB are obtained when the composite thickness is 3.5 mm. The prepared multilayer absorbing composites can adapt to a variety of application scenarios and have excellent application prospects in the industry. The self‐polymerization of dopamine and complexation of metal ions were used to construct multilayer absorbing materials, and the dielectric loss and magnetic loss capacity of the carbon fibers improved.

Design of New Schiff Bases and Their Heavy Metal Ion Complexes for Environmental Applications: A Molecular Dynamics and Density Function Theory Study.

Schiff bases (SBs) are important ligands in coordination chemistry due to their unique structural properties. Their ability to form complexes with metal ions has been exploited for the environmental detection of emerging water contaminants. In this work, we evaluated the complexation ability of three newly proposed SBs, 1-3, by complete conformational analysis, using a combination of Molecular Dynamics and Density Functional Theory studies, to understand their ability to coordinate toxic heavy metal (HMs) ions. From this study, it emerges that all the ligands present geometries that make them suitable to complex HMs through the N-imino moieties or, in the case of 3, with the support of the oxygen atoms of the ethylene diether chain. In particular, this ligand shows the most promising coordination behavior, particularly with Pb2+.

Endowing Metal-Organic Coordination Materials with Chiroptical Activity by a Chiral Anion Strategy.

Recently, chiral metal-organic coordination materials have emerged as promising candidates for a wide range of applications in chiroptoelectronics, chiral catalysis, and information encryption, etc. Notably, the chiroptical effect of coordination chromophores makes them appealing for applications such as photodetectors, OLEDs, 3D displays, and bioimaging. The direct synthesis of chiral coordination materials using chiral organic ligands or complexes with metal-centered chirality is very often tedious and costly. In the case of ionic coordination materials, the combination of chiral anions with cationic, achiral coordination compounds through noncovalent interactions may endow molecular materials with desirable chiroptical properties. The use of such a simple chiral strategy has been proven effective in inducing promising circular dichroism and/or circularly polarized luminescence signals. This concept article mainly delves into the latest advances in exploring the efficacy of such a chiral anion strategy for transforming achiral coordination materials into chromophores with superb photo- or electro-chiroptical properties. In particular, ionic small-molecular metal complexes, metal clusters, coordination supramolecular assemblies, and metal-organic frameworks containing chiral anions are discussed. A perspective on the future opportunities on the preparation of chiroptical materials with the chiral anion strategy is also presented.

Synthesis, Characterization and Bioactivity Evaluation for Some Metal Ions Complexes with New Ligand Derived from 2-hydroxy-1- napthaldehyed

تم مفاعلة قاعدة شيف المُحضرة حديثًا (E)-2-((2-phenylhydrazono)methyl)naphthalen-1-ol (مشتق فينيل هيدرازين) مع كل من الأيونات المعدنية التالية: Ni2 + ، Cu2 + Zn2 + , Cd2+للحصول على معقدات فلزية بأشكال هندسية مختلفة. تم الاستدلال عن تكوين معقدات قاعدة شيف وأيضًا قاعدة شيف الأصلية باستخدام كروماتوغرافيا السائل-مطياف الكتلة التي تتفق مع الكتلة المولية التي تم الحصول عليها نظريا، أثبت دراسات مطيافية الاشعة تحت الحمراءحدوث التناسق من خلال N من azobenzene و اوكسجين مجموعة ال OH من خلال ملاحظة الانزياح في قمةazomethines والظهور كل من قمتيM-N و N-O. علاوة على ذلك ، يمكننا أيضًا أن نكتشف بواسطة هذا الجهاز وجود جزيء ماء داخل مجال التناسق. كشفت أطياف UV-Vis لجميع النتائج عن حدوث تناسق من خلال ملاحظة الانزياح في الانتقالات الإلكترونية التي حدثت في الليكاند في المنطقة فوق البنفسجية. تثبت قياسات TGA و DSC لكل من الليكاند و معقد النيكل أيضًا تكون المعقد ووجود جزيء ماء داخل مجال التناسق. بالإضافة إلى ذلك ، كانت نتائج التوصيلية المولارية و الامتصاص الذري اللهبي FAA أقرب إلى نتائج المحسوبة نظريا. أعطت نتائج التشخيص معقدات أحادية النواة وسلوك ثنائي السن واشكال هندسية رباعي السطوح لجميع المعقدات. اعتمادا على خاصية المضادات الحيوية لقاعدة شيف ومعقداتها ، قمنا بدراسة الفعالية الحيوية لقاعدة شف ومعقداتها كما مفصل في المخطوطة.

CATALYTIC ACTIVITY OF METAL-BASED IONIC LIQUIDS IN OXIDATIVE DESULFURIZATION

Effective desulfurization techniques are required due to the operational and environmental difficulties caused by sulfur compounds found in petroleum fuels. The use of Fenton catalysts in the oxidative desulfurization of petroleum fuels is examined in this work. Evaluating the viability and effectiveness of Fenton catalysts in lowering sulfur concentration while maintaining fuel quality is the main goal. Promising outcomes are found in laboratory tests using hydrogen peroxide (H2O₂) and ferrous iron (Fe³⁺) as catalysts. Fenton catalysts focus on sulfur compounds and transform them into forms that are soluble in water, making the process of separating them from the fuel easier. This procedure offers a more environmentally friendly and financially feasible desulfurization option because it works in milder circumstances than other techniques. The results provide a viable path for the development of sustainable fuel and have ramifications for greener energy sources and environmental legislation. There has been a growing interest in ionic liquids (ILs) as innovative materials for functional desulfurization. Based on their definition and fundamental structure, metal-based ionic liquids (MILs) are divided into three categories in this critical article: metal chloride MILs, metal oxide MILs, and metal complex MILs. To enhance the oxidative desulfurization (ODS) process, MILs have both the oxidation and absorption sites for intramolecular adsorption and oxidation. A noteworthy characteristic of MILs in ODS is biomimetic catalysis, which serves to enhance oxidation performance by triggering molecular oxygen. Hydrogen peroxide or oxygen combined with the available water, together with metal oxide and metal complex ions, create a Fenton-like reaction that transforms hydrophobic organic sulfur (SO2) or hydrophilic sulfoxide/sulfone (Seroxide), or sulfur acid, respectively. Promising approaches for developing environmentally friendly and highly effective desulfurization procedures for large-scale applications are also given. Keywords: supported ionic liquid catalyst (SILC), hydrogen peroxide, catalytic oxidative desulfurization, copper (I) chlorocomplexes.

Preparation and Characterization of Periwinkle Shell Based Chitosan-Kenaf fibre Copolymer and its Derivatives for Selective Binding of Cu (II) and Zn (II) ions from Electroplating Effluent

The levels of heavy metal in industrial waste streams, if not remediated before discharge to eco-system, could pose a threat to flora and fauna. The objective of this study was to evaluate the suitability of a novel adsorbent materials from periwinkle shell-based chitosan-kenaf fibre copolymer and its ethylene glycol diglycidyl ether crosslinked derivatives for the selective removal of Cu2+and Zn2+ from electroplating effluent using batch experimental protocol. Results showed that the crosslinked copolymers were more effective for the sorption of these metal ions from effluent solution with percentage sorption range of 76-87% and 84-93% for Cu2+ and Zn2+ respectively. Kinetic data depicts pseudo-second-order model fits for the adsorbent materials and confirm chemosorption as the mechanism for metal ion complexation with adsorbent surfaces. Based on R2 correlation values, sorption of the metal ions by the pristine adsorbent materials fit well with Langmuir isotherm model, in contrast, those for crosslinked adsorbent materials were best described by Freundlich isotherm model. The results present the adsorbent materials with auspicious potentials, especially the crosslinked derivatives, and stand them in exceptional good stead as suitable bioresource materials for column packing in waste abatement equipment for remediation of these metal ions from electroplating effluent solution.

A molecular extraction process for vanadium based on tandem selective complexation and precipitation

Recycling vanadium from alternative sources is essential due to its expanding demand, depletion in natural sources, and environmental issues with terrestrial mining. Here, we present a complexation-precipitation method to selectively recover pentavalent vanadium ions, V(V), from complex metal ion mixtures, using an acid-stable metal binding agent, the cyclic imidedioxime, naphthalimidedioxime (H2CIDIII). H2CIDIII showed high extraction capacity and fast binding towards V(V) with crystal structures showing a 1:1 M:L dimer, [V2(O)3(C12H6N3O2)2]2−, 1, and 1:2 M:L non-oxido, [V(C12H6N3O2)2] ̶ complex, 2. Complexation selectivity studies showed only 1 and 2 were anionic, allowing facile separation of the V(V) complexes by pH-controlled precipitation, removing the need for solid support. The tandem complexation-precipitation technique achieved high recovery selectivity for V(V) with a selectivity coefficient above 3 × 105 from synthetic mixed metal solutions and real oil sand tailings. Zebrafish toxicity assay confirmed the non-toxicity of 1 and 2, highlighting H2CIDIII’s potential for practical and large-scale V(V) recovery.

Study of Physiological and Pharmacological Properties of Hydrochlorothiazide Schiff Base and its Metal Ion Complex

The current study focuses on the synthesis and the biological evaluation of Schiff base metal complex produced from the diuretic drug Hydrochlorothiazide. The bidentate ligand is produced by inserting salicylaldehyde into a 1:1 molar ratio and condensing 6-chloro-1,1-dioxo-3,4-dihydro-2H-1λ6,2,4-benzothiadiazine -7-sulfonamide. Complex of Co(II) with general formula ML2 have been produced using this bidentate ligand. We examined the antibacterial properties of the produced compounds. The results that were achieved were compared with the original medicine, hydrochlorothiazide. The compounds exhibited enhanced antibacterial assay, with the Co(II) complex demonstrating especially strong activity. The ligand and its complex Co(II) were also screened for the invivo Diuretic techniques.

Luminescent Properties Variation Caused by Metal Cations Effect on the Deep Energy Levels in Cu(I) and Ag(I) Complexes

AbstractIn this work, a donor‐acceptor (D‐A) type ligand is prepared to construct Cu(I) and Ag(I) complexes. These complexes possess similar molecular structures, distributions of molecular orbitals, and distributions of electrons and holes in excited states. However, they exhibit distinct photophysical properties, such as luminescent spectra and transient photo‐luminescent decay spectra. Through analysis of deep‐lying molecular orbitals in a tetrahedral field, it is determined that the variation in d‐p π conjugation between the metal cation's d‐orbitals and the π orbitals of the electron‐acceptor part of the D‐A ligand is the reason for the different photophysical properties. This research contributes to an in‐depth understanding of the role of metal ions in luminescent complexes, providing insights from the perspective of coordination chemistry.

A One‐Pot Synthesized Chemodosimetric Chemosensor for Highly Sensitive Cyanide Ion Detection in Aqueous Media and from Tobacco Smoke

AbstractA sustainable future world consistently attributes to the development of eco‐friendly methods and materials for detection and elimination of toxic substances from the environment. While addressing the issues, pyrazole carbonitrile derived Schiff base PYR−TZ has been designed and employed for colorimetric and turn on fluorometric cyanide ion sensing. PYR−TZ demonstrated high cyanide ion (CN−) sensitivity with a 1 : 1 binding stoichiometry in aqueous solution. By preventing intramolecular charge transfer, the PYR−TZ sensor demonstrated excellent selectivity towards CN, which caused a color transition from colorless to yellow and impressive “turn‐on” fluorescence emission. The detection thresholds for CN− are 6.5 nm for absorbance spectra and 0.396 nm emission spectra, respectively. Under typical ecological and physiological settings (pH 1–12), the PYR−TZ sensor can function as an effective chemical sensor for detecting the CN− ions. Additionally, the sensor can find CN in tobacco commercial products like cigarettes and cigars. PYR−TZ is a great cyanide sensor probe that has a number of benefits, which includes simple synthesis, distinct color and emission change, a high degree of selectivity, lesser limit of detection, reversibility, and good anti‐interference ability to analyze solution and tobacco commercial things, together with fluorescence imaging. The theoretical optimized structure and electronic transitions were confirmed by DFT and TDDFT studies. On the basis of theoretical and experimental calculations (DFT), the mechanism of the metal ion complex is postulated.

املاح الفلزات الانتقالية الأولى للدايازونيوم المشتق من مركب حلقي غير متجانس للنيتروجين تحضيرو تشخيص و الفعالية الحيوية

يتضمن البحث تحضيرمعقدات لايونات الكروم (III) والمنغنيز (II) والحديد (III) والكوبلت (II) والتيكل (II) والنحاس (II) والخارصين (II) مع (3- امينو -2- کلوروبیریدین) ديازونيوم ذات الصيغة [Cl-C5H3N=N]n[MXm], حيث ان n=2 او 3 و 4=m او 6 للايونات ثنائية او ثلاثية التكافؤعلى التوالي . شخصت المعقدات المحضرة بوساطة الامتصاص الذري والتحليل الدقيق للعناصر .C.H.N والتوصيلية الكهربائية وطيف الاشعة تحت الحمراء والاطياف الالكترونية وطيف الرنين النووي المغناطيسي للبروتون وقياسات الحساسية المغناطيسية بالاضافة الى التحاليل الحرارية TGA و DTA اظهرت القياسات ان معقدات العناصر ثنائية التكافؤ تكون بنسبة مولية 1:2 (ليكند: فلز) وتمتلك شكل هندسي رباعي السطوح حول الايون الفلزي في حين تمتلك ايونات الفلزات ثلاثية التكافؤ شكل هندسي ثماني السطوح وبنسبة مولية (1:3) (ليكند: فلز) . ودرست الفعالية الحيوية تجاه نوعين من البكتريا Gram, positive (Staphylococcus aureus) , Gram, negative (Klebsieiaella pneumonia)) حيث اظهرت المعقدات 2 و 3 و 5 و 6 فعالية متوسطة في حين المعقدان 1 و 7 اظهرتا فعالية عالية مقارنة مع المادة القياسية.

Fabrication of an Ultrastrong Formaldehyde-Free Wood Adhesive with an Organic-Inorganic Cross-Linking Network.

The wood industry faces challenges in producing eco-friendly, high-performance, and formaldehyde-free adhesives. In this study, carboxylated styrene-butadiene rubber (XSBR) was blended with polyamidoamine-epichlorohydrin (PAE) resin, and a controlled amount of CaCO3 powder was incorporated to create an adhesive with exceptional strength. The resulting three-layer plywood demonstrated remarkable dry and wet shear strengths of 3.09 and 2.36 MPa, respectively, and of 2.27 MPa after boiling water tests, comparable to that of phenolic resins. Additionally, the adhesive exhibited strong adhesion across various materials including glass, metal, etc. This exceptional performance was due to two primary factors: (1) the high-density chemical cross-linking reaction and the physical entanglement between XSBR and PAE; (2) the organic-inorganic hybrid involving metal ion complexation developed by CaCO3, which fostered molecular chain connections and enhanced the adhesive-material interface. These findings offer valuable references for further research in the field of wood adhesives.

Synthesis and Characterization of 4-(1-(2H benzo[d][1,2,3]triazol-2-ylimino)ethyl)benzonitrile and amino acid alanine and its Metal Complexes

The biological actions of transition metal ion complexes with mixed ligands are very different. Amino acid and azomethine containing Schiff bases are very useful building blocks for ternary complexes. The interaction of two ligands 4-(1-(2H-benzo[d][1,2,3]triazol-2-ylimino)ethyl)benzonitrile as L1 and an amino acid alanine as L2, with newly synthesized cuprous chloride solution in a 1:1:1 molar ratio using standard reflux approach has been attempted to create unique metal(I) complexes. Elemental analysis, molecular weight, magnetic moment, thermal analysis and spectroscopic methods are used to characterize the produced ligand and metal(I) complexes. Bacillus subtilis, Escherichia coli and Candida albicans were used as test organisms in antibacterial tests of the produced compounds. Antibacterial and antifungal activity of the metal (I) complexes have been shown to be very high against ciprofloxacin, ketoconazole.

Hydration characteristics of steel slag in the presence of diethanol-isopropanolamine

Steel slag (SS) as a supplementary cementitious material has low cementitious activity. Diethanol-isopropanolamine (DEIPA) is an organic admixture that can enhance the cementitious activity of cementitious materials. This work aimed to investigate the hydration characteristics of SS under the complexing of DEIPA. The hydration process of SS, the complexation of DEIPA with metal ions, and the dissolution process of C3A and C3S in the presence of DEIPA were systematically investigated. The results showed that DEIPA enhanced the hydration of aluminate (C3A and C12A7), ferrate (C2F) and silicate phases (C3S and C2S), which formed a large amount of monocarboaluminate, paraalumohydrocalcite and C–S–H gels. In the early stages of hydration, the hydration products were mainly C–S–H gels, monocarboaluminate and paraalumohydrocalcite, and in the later stages of hydration, the hydration products were mainly C–S–H gels, paraalumohydrocalcite. The monocarboaluminate may be transformed to paraalumohydrocalcite at a later stage. This hydration-promoting effect was related to the complexation of DEIPA. DEIPA facilitated the dissolution of mineral phases and the precipitation of complexed metal ions by complexing with metal ions. The stronger complexation of Al3+ by DEIPA made it more solubilizing for C3A. As a result, more aluminum-containing hydration products were formed. The weaker complexation of Ca2+ by DEIPA made it a weaker solubilizing for C3S, which also led to a weaker promotion of silicate hydration by DEIPA. The solubilization of DEIPA to minerals enhanced the cementitious activity of SS, which ultimately led to the increase in the compressive strength of the hardened SS paste at each age.