Its related to Study of gene metal-ligand stability constant of cefadroxil with cu2+ metal ion ph metrically at 0.1 m ionic strength. Also describe another Parameters.
The factors that affect the stability of complexes Ernest Opoku
The stability of metal complexes is affected by various ligand and metal factors. Ligand factors that increase stability include small size, high charge, chelation which forms multiple bonds to the metal, and high basicity. Steric effects from bulky ligands decrease stability. For the metal, higher charge and smaller size increase stability, as do behaviors defined by the Ahrland-Chatt classification like class A metals forming more stable complexes with lighter donor atoms. The Irving-Williams series and crystal field theory show transition metal complex stability follows trends based on ionic radius, crystal field splitting, and effects like Jahn-Teller distortion.
This document discusses chelates and the chelate effect. It defines chelates as coordination complexes containing ligands bonded to a central metal atom at two or more points, forming ring structures. The chelate effect refers to chelated complexes being more stable than similar non-chelated complexes due to an increase in entropy. Factors that influence the stability of chelated complexes include the number of donor atoms in the ligand, the size of the metal-ligand rings formed, and the presence of double bonds in the ligand.
The document discusses coordination compounds and Werner's postulates. It provides answers to multiple questions related to coordination compounds, including examples of coordination entities, ligands, coordination numbers, isomerism in coordination compounds, and IUPAC naming of coordination compounds. Specific examples discussed include [Co(NH3)6]Cl3, [Pt(NH3)2Cl(NH2CH3)]Cl, and the isomers of [CoCl2(en)2]+.
Chapter 17 complexation and precipitation reactions and titrationsCleophas Rwemera
This document discusses complexation reactions and titrations. It notes that complexation reactions are widely used in analytical chemistry, such as for titrating cations. Some complexes are colored or absorb ultraviolet radiation, making them useful for spectrophotometric analysis. Additionally, some complexes have low solubility and can be used for precipitation titrations or gravimetric analysis. The document focuses on the formation of complexes between metal ions and ligands through coordination bonds. It discusses factors that influence complex formation such as ligand type, metal coordination number, and solution pH. The thermodynamics of stepwise complex formation are also examined.
This document provides an overview of metal complexes and organometallics. It discusses the structure, bonding, and applications of inorganic complexes and coordination compounds. Key topics covered include ligands, isomerism, crystal field theory, and the spectrochemical series. Organometallics such as metal carbonyls, ferrocene, and Grignard reagents are also introduced. Important applications of coordination compounds are highlighted in areas like extraction of metals, analytical chemistry, biology, medicine, and industry.
Organometallic Reactions and CatalysisRajat Ghalta
Organometallic compounds undergo a rich variety of reactions (oxidative addition, reductive elimination, cyclometalization, migratory insertion, carbonylation, hydrometallation hydrate elimination, etc ) that can sometimes be combined into useful homogeneous catalytic cycles. In this presentation, I have discussed organometallic reactions of particular importance for synthetic and catalytic processes like the oxo process (hydroformylation), heck coupling reaction, Wilkinson’s Catalyst
(Hydrogenation) etc.
This document provides an introduction to organometallic compounds. It defines organometallic compounds as those containing at least one metal-carbon bond. It discusses some of the main applications of organometallics in industries like pharmaceuticals and semiconductors. The document then covers various topics related to organometallics including their classification, nomenclature, preparation methods like metathesis and transmetallation reactions, and examples of important organometallic compounds like alkylaluminums.
Metal carbonyls are coordination complexes of transition metals with carbon monoxide ligands. They were first synthesized in 1868 by passing carbon monoxide over platinum. Metal carbonyls typically obey the 18 electron rule and are often diamagnetic. They have applications as catalysts in organic synthesis and in producing pure metals like nickel. Precautions must be taken when using metal carbonyls due to their toxicity.
The factors that affect the stability of complexes Ernest Opoku
The stability of metal complexes is affected by various ligand and metal factors. Ligand factors that increase stability include small size, high charge, chelation which forms multiple bonds to the metal, and high basicity. Steric effects from bulky ligands decrease stability. For the metal, higher charge and smaller size increase stability, as do behaviors defined by the Ahrland-Chatt classification like class A metals forming more stable complexes with lighter donor atoms. The Irving-Williams series and crystal field theory show transition metal complex stability follows trends based on ionic radius, crystal field splitting, and effects like Jahn-Teller distortion.
This document discusses chelates and the chelate effect. It defines chelates as coordination complexes containing ligands bonded to a central metal atom at two or more points, forming ring structures. The chelate effect refers to chelated complexes being more stable than similar non-chelated complexes due to an increase in entropy. Factors that influence the stability of chelated complexes include the number of donor atoms in the ligand, the size of the metal-ligand rings formed, and the presence of double bonds in the ligand.
The document discusses coordination compounds and Werner's postulates. It provides answers to multiple questions related to coordination compounds, including examples of coordination entities, ligands, coordination numbers, isomerism in coordination compounds, and IUPAC naming of coordination compounds. Specific examples discussed include [Co(NH3)6]Cl3, [Pt(NH3)2Cl(NH2CH3)]Cl, and the isomers of [CoCl2(en)2]+.
Chapter 17 complexation and precipitation reactions and titrationsCleophas Rwemera
This document discusses complexation reactions and titrations. It notes that complexation reactions are widely used in analytical chemistry, such as for titrating cations. Some complexes are colored or absorb ultraviolet radiation, making them useful for spectrophotometric analysis. Additionally, some complexes have low solubility and can be used for precipitation titrations or gravimetric analysis. The document focuses on the formation of complexes between metal ions and ligands through coordination bonds. It discusses factors that influence complex formation such as ligand type, metal coordination number, and solution pH. The thermodynamics of stepwise complex formation are also examined.
This document provides an overview of metal complexes and organometallics. It discusses the structure, bonding, and applications of inorganic complexes and coordination compounds. Key topics covered include ligands, isomerism, crystal field theory, and the spectrochemical series. Organometallics such as metal carbonyls, ferrocene, and Grignard reagents are also introduced. Important applications of coordination compounds are highlighted in areas like extraction of metals, analytical chemistry, biology, medicine, and industry.
Organometallic Reactions and CatalysisRajat Ghalta
Organometallic compounds undergo a rich variety of reactions (oxidative addition, reductive elimination, cyclometalization, migratory insertion, carbonylation, hydrometallation hydrate elimination, etc ) that can sometimes be combined into useful homogeneous catalytic cycles. In this presentation, I have discussed organometallic reactions of particular importance for synthetic and catalytic processes like the oxo process (hydroformylation), heck coupling reaction, Wilkinson’s Catalyst
(Hydrogenation) etc.
This document provides an introduction to organometallic compounds. It defines organometallic compounds as those containing at least one metal-carbon bond. It discusses some of the main applications of organometallics in industries like pharmaceuticals and semiconductors. The document then covers various topics related to organometallics including their classification, nomenclature, preparation methods like metathesis and transmetallation reactions, and examples of important organometallic compounds like alkylaluminums.
Metal carbonyls are coordination complexes of transition metals with carbon monoxide ligands. They were first synthesized in 1868 by passing carbon monoxide over platinum. Metal carbonyls typically obey the 18 electron rule and are often diamagnetic. They have applications as catalysts in organic synthesis and in producing pure metals like nickel. Precautions must be taken when using metal carbonyls due to their toxicity.
Chemical bonding involves atoms forming stable electronic configurations through gaining, losing or sharing electrons. Ionic bonds form between metals and nonmetals when electrons are transferred, while covalent bonds involve sharing electron pairs between nonmetals to achieve stable octets. Different bond types including ionic, covalent and metallic bonding can be identified based on the participating elements and electron configurations involved.
This document discusses coordination chemistry and isomerism in coordination compounds. It defines molecular compounds, complex salts, and double salts formed from combinations of inorganic salts. It also discusses ligands, classifying them based on properties. Coordination number and the resulting geometries for coordination numbers 2 through 9 are described. Finally, it outlines different types of isomerism that can occur in coordination compounds, including structural, spin, and stereo isomerism.
This document discusses coordination chemistry, including the concepts of labile and inert complexes, factors that affect stability and lability, and theories of the trans effect. It also briefly outlines the structures of chlorophyll, hemoglobin, and vitamin B12. Labile complexes rapidly exchange ligands while inert complexes exchange ligands slowly. Stability is influenced by factors like the metal ion size and charge, as well as ligand properties. The polarization and pi-bonding theories explain the trans effect, in which ligands trans to certain others make that site more reactive.
Reductive elimination is an elementary step where the metal's coordination number and oxidation state both decrease as a new covalent bond is formed. It is the reverse of oxidative addition. Reductive elimination is more common for metals in higher oxidation states. For reductive elimination to occur, the eliminating groups must be cis-oriented and there must be a high formal positive charge on the metal. Reductive elimination finds applications in important catalytic reactions like hydrogenation and hydroformylation.
Physical and analytical studies of transition metal complexes Huda Eid
This document discusses physical and analytical studies of transition metal complexes. It begins by defining transition metal complexes as having a central metal ion bonded to surrounding ligand molecules by coordinate bonds. The document then discusses various properties of complexes including geometry, stereoisomerism, magnetism, color formation, stability, and catalytic properties. Finally, it outlines several classical and instrumental analytical methods used to study complexes, such as qualitative and quantitative chemical analysis, spectroscopy, separation techniques like chromatography, and X-ray crystallography.
This document summarizes key concepts in organometallic chemistry. It discusses the definition of organometallic compounds as those containing metal-carbon bonds. It outlines different types of ligands that can bind to metals, including carbonyl, carbene, and cyclic π systems. It also describes principles for understanding bonding interactions between ligands and metals, such as the 18-electron rule and molecular orbital theory. Spectroscopic techniques for analyzing organometallic compounds are also summarized.
Assignment chemical bonding_jh_sir-4163NEETRICKSJEE
This document contains information about chemical bonding. It begins with an introduction to chemical bonds, including the causes of chemical combination and classification of different bond types. It then discusses ionic bonds in depth, including how they form through electron transfer, representation of ionic compound formulas, and factors that affect ionic bond strength. The document also covers properties of ionic compounds such as physical state, isomorphism, conductivity, solubility, and polarization.
This presentation discusses back-donation of CO ligands to transition metals. Back-donation occurs when electrons from the metal's d-orbitals are donated into the CO ligand's anti-bonding π* orbital, weakening the carbon-oxygen bond. CO can bind to single metals through both sigma and pi bonding. It can also bridge between multiple metal atoms, further weakening the carbon-oxygen bond. Infrared spectroscopy shows that as more metals are involved in back-donation to a CO ligand, its carbon-oxygen stretching frequency decreases due to the bond being more weakened.
The document discusses the lability and inertness of coordination complexes. It defines labile complexes as those where ligand exchange occurs rapidly, while inert complexes have slow ligand exchange. Lability is determined by factors like the metal ion size, charge, and d-electron configuration, not thermodynamic stability. Smaller or higher charged metal ions and complexes with less than 3 d-electrons tend to be more labile. The rate of ligand substitution depends on both the leaving and entering ligands. Steric effects and solvent also influence the rate. Complexes may undergo dissociative or associative substitution based on their structure.
1. Organometallic compounds are defined as compounds in which carbon atoms are directly bonded to metal atoms. Organometallic compounds can be classified as ionic, covalent, or electron deficient based on the nature of the metal-carbon bond.
2. Metal carbonyls are compounds where carbon monoxide ligands are bonded directly to metal centers. They can be mononuclear, containing one metal center, or polynuclear, containing multiple metal centers. Common mononuclear metal carbonyls prepared include nickel tetracarbonyl, iron pentacarbonyl, and chromium hexacarbonyl.
3. The document provides details on the nomenclature, classification, preparation, and structures
The document discusses different types of isomerism seen in coordination compounds, including structural isomerism (ionization, polymerization, hydrate, linkage, coordination, ligand isomerism) and stereoisomerism (geometric, optical isomerism). It provides examples of each type of isomerism. It also discusses the number of possible isomers for coordination compounds based on their coordination number and ligand arrangement.
Concept of oxidation and reduction, redox reactions, oxidation number, balancing redox reactions, loss and gain of electrons, Balancing redox reactions, Half reaction method, Types of redox reaction- direct and indirect method, Electrochemical cell, Classification of redox reactions.
This document provides information about coordination compounds and Werner's theory of coordination compounds. It begins with an overview of coordination compounds and their importance. It then discusses Werner's theory, including his postulates about primary and secondary valences of metal ions and the coordination number being equal to the number of ligands bound to the metal ion. The document defines key terms related to coordination compounds such as coordination entity, central atom/ion, ligands, coordination number, and isomers. It also discusses nomenclature rules for writing formulas and names of mononuclear coordination compounds. The summary is as follows:
1) The document discusses Werner's pioneering theory of coordination compounds and key postulates about metal ion valences and coordination geometry
1. The document discusses transition metal complexes, including their properties and bonding models.
2. Key topics covered include ligand field theory, isomerism in complexes, naming complexes using IUPAC rules, and the electronic spectra and magnetic properties used to evaluate bonding models.
3. Several bonding models are mentioned, including Werner's theory, Sidgwick's theory, crystal field theory, and ligand field theory.
This document provides information about transition metals and their coordination compounds. It discusses the colors of representative compounds of period 4 transition metals. It also discusses properties of group 6B elements chromium, molybdenum, and tungsten. The document explains that lanthanides have similar properties and most have the electron configuration [Xe]6s24f1-14. It provides examples of coordination compounds and defines coordination number and common geometries of complex ions. Common ligands are identified and the concept of chelates is described. Formulas of coordination compounds are explained and how to determine the charge of the metal ion. The document concludes with descriptions of how to name coordination compounds.
This document discusses complexometric titrations using ethylenediaminetetraacetic acid (EDTA) as the titrant. It describes how EDTA forms stable 1:1 complexes with metal ions and can be used to titrate metals in various ways, including direct titration, back-titration, and replacement titration. It also explains the importance of pH and discusses indicators used for different metal-EDTA complexes. Calcium titrations are discussed as an example, noting how magnesium ions improve the sharpness of the endpoint when using solochrome black indicator.
This document provides an introduction to transition metal complexes. It discusses the aqueous chemistry of metal ions, including hydrolysis. Hexaaqua ions form when transition metals dissolve in water and are surrounded by six water molecules in an octahedral structure. Hydrolysis occurs when water molecules attack these complexes, removing protons and forming hydroxide ions. This makes the solution acidic. The document also discusses stability constants, which are equilibrium constants for the formation of complex ions from their constituent parts. Higher stability constants indicate more stable complexes.
This document discusses coordination compounds and their structures and isomers. It covers Werner's coordination chemistry theories, ligand types including chelating ligands, nomenclature of coordination compounds, and isomerism including geometric and chiral isomers. It also discusses factors that determine coordination numbers and common coordination number structures.
Synthesis, Characterization and Antibacterial Activity of New Complexes of So...IOSR Journals
Complexes of some lanthanide picrates (Ln3+ = Pr3+, Nd3+ and Dy3+) with benzo-18-crown-6 and 221-cryptand were synthesized and characterized by elemental analysis, FTIR, and UV-Visible. Spectrophotometric methods, thermal analysis (TGA & DTG), melting point, magnetic susceptibility and molar conductance. Also an in-vitro study on gram positive (Staphylococcus aureus) and gram negative bacteria (Escherichia coli, Salmonella and pseudomonas aeruginosa) was performed and the results were compared to those of the broad spectrum antibiotic Chloramphinicol. The benzo-18-crown-6 complexes have the general formula of [Ln.L.(Pic)2]Pic.nH2O , where; (Ln3+ = Pr3+, Nd3+, and Dy3+) , (L = Benzo-18-crown-6) , (Pic = Picrate anion) , (n = 1-2). In these complexes two picrate anions are coordinated to the metal ion through the phenolic oxygen and oxygen of the ortho nitro group, thus, the metal ions in these complexes have a coordination number of (10). The complexes of 221-cryptand have the general formula of [Ln.L.(Pic)]Pic2.nH2O where; (Ln3+ = Pr3+, Nd3+, and Dy3+), (L = 221-cryptand), (Pic = Picrate anion), (n = 1,2 or 7). In these complexes one picrate anion is coordinated to the metal ion, also through the phenolic oxygen and the oxygen from the ortho nitro group, thus the metal ions in the cryptand complexes have a coordination number of (9).
Synthesis, Spectroscopic Studies and Antibacterial Activity of Novel Schiff B...IRJET Journal
The document describes the synthesis and characterization of novel Schiff base metal complexes derived from condensation of 5-bromosalicylaldehyde, 4,5-dichloro-o-phenylenediamine, and pentane-2,4-dione. Specifically, copper(II), nickel(II), and oxovanadium(IV) complexes were synthesized and characterized using analytical, spectral, electrochemical, and antimicrobial methods. The complexes were found to have general formula [M(L)]X where M is the metal and L is the tetradentate Schiff base ligand. Spectroscopic data indicated the ligand coordinates through the hydroxyl oxygen and azomethine nitrogen. The metal complexes
IRJET- Equilibrium Studies on Ternary Metal Complexes of Drug Ethambutol Hydr...IRJET Journal
This document discusses the equilibrium studies of ternary metal complexes formed between transition metal ions (nickel and cobalt), the drug ethambutol hydrochloride, and four amino acids (serine, valine, methionine, and glutamic acid). The stability constants of the binary and ternary complexes were determined using pH-metric titration methods. The results showed that the stability of the ternary complexes was higher than the corresponding binary complexes, as indicated by preferential formation and positive relative stability parameters. Specifically, cobalt complexes with serine and nickel complexes with glutamic acid had the highest stability constants among the ternary systems studied.
Chemical bonding involves atoms forming stable electronic configurations through gaining, losing or sharing electrons. Ionic bonds form between metals and nonmetals when electrons are transferred, while covalent bonds involve sharing electron pairs between nonmetals to achieve stable octets. Different bond types including ionic, covalent and metallic bonding can be identified based on the participating elements and electron configurations involved.
This document discusses coordination chemistry and isomerism in coordination compounds. It defines molecular compounds, complex salts, and double salts formed from combinations of inorganic salts. It also discusses ligands, classifying them based on properties. Coordination number and the resulting geometries for coordination numbers 2 through 9 are described. Finally, it outlines different types of isomerism that can occur in coordination compounds, including structural, spin, and stereo isomerism.
This document discusses coordination chemistry, including the concepts of labile and inert complexes, factors that affect stability and lability, and theories of the trans effect. It also briefly outlines the structures of chlorophyll, hemoglobin, and vitamin B12. Labile complexes rapidly exchange ligands while inert complexes exchange ligands slowly. Stability is influenced by factors like the metal ion size and charge, as well as ligand properties. The polarization and pi-bonding theories explain the trans effect, in which ligands trans to certain others make that site more reactive.
Reductive elimination is an elementary step where the metal's coordination number and oxidation state both decrease as a new covalent bond is formed. It is the reverse of oxidative addition. Reductive elimination is more common for metals in higher oxidation states. For reductive elimination to occur, the eliminating groups must be cis-oriented and there must be a high formal positive charge on the metal. Reductive elimination finds applications in important catalytic reactions like hydrogenation and hydroformylation.
Physical and analytical studies of transition metal complexes Huda Eid
This document discusses physical and analytical studies of transition metal complexes. It begins by defining transition metal complexes as having a central metal ion bonded to surrounding ligand molecules by coordinate bonds. The document then discusses various properties of complexes including geometry, stereoisomerism, magnetism, color formation, stability, and catalytic properties. Finally, it outlines several classical and instrumental analytical methods used to study complexes, such as qualitative and quantitative chemical analysis, spectroscopy, separation techniques like chromatography, and X-ray crystallography.
This document summarizes key concepts in organometallic chemistry. It discusses the definition of organometallic compounds as those containing metal-carbon bonds. It outlines different types of ligands that can bind to metals, including carbonyl, carbene, and cyclic π systems. It also describes principles for understanding bonding interactions between ligands and metals, such as the 18-electron rule and molecular orbital theory. Spectroscopic techniques for analyzing organometallic compounds are also summarized.
Assignment chemical bonding_jh_sir-4163NEETRICKSJEE
This document contains information about chemical bonding. It begins with an introduction to chemical bonds, including the causes of chemical combination and classification of different bond types. It then discusses ionic bonds in depth, including how they form through electron transfer, representation of ionic compound formulas, and factors that affect ionic bond strength. The document also covers properties of ionic compounds such as physical state, isomorphism, conductivity, solubility, and polarization.
This presentation discusses back-donation of CO ligands to transition metals. Back-donation occurs when electrons from the metal's d-orbitals are donated into the CO ligand's anti-bonding π* orbital, weakening the carbon-oxygen bond. CO can bind to single metals through both sigma and pi bonding. It can also bridge between multiple metal atoms, further weakening the carbon-oxygen bond. Infrared spectroscopy shows that as more metals are involved in back-donation to a CO ligand, its carbon-oxygen stretching frequency decreases due to the bond being more weakened.
The document discusses the lability and inertness of coordination complexes. It defines labile complexes as those where ligand exchange occurs rapidly, while inert complexes have slow ligand exchange. Lability is determined by factors like the metal ion size, charge, and d-electron configuration, not thermodynamic stability. Smaller or higher charged metal ions and complexes with less than 3 d-electrons tend to be more labile. The rate of ligand substitution depends on both the leaving and entering ligands. Steric effects and solvent also influence the rate. Complexes may undergo dissociative or associative substitution based on their structure.
1. Organometallic compounds are defined as compounds in which carbon atoms are directly bonded to metal atoms. Organometallic compounds can be classified as ionic, covalent, or electron deficient based on the nature of the metal-carbon bond.
2. Metal carbonyls are compounds where carbon monoxide ligands are bonded directly to metal centers. They can be mononuclear, containing one metal center, or polynuclear, containing multiple metal centers. Common mononuclear metal carbonyls prepared include nickel tetracarbonyl, iron pentacarbonyl, and chromium hexacarbonyl.
3. The document provides details on the nomenclature, classification, preparation, and structures
The document discusses different types of isomerism seen in coordination compounds, including structural isomerism (ionization, polymerization, hydrate, linkage, coordination, ligand isomerism) and stereoisomerism (geometric, optical isomerism). It provides examples of each type of isomerism. It also discusses the number of possible isomers for coordination compounds based on their coordination number and ligand arrangement.
Concept of oxidation and reduction, redox reactions, oxidation number, balancing redox reactions, loss and gain of electrons, Balancing redox reactions, Half reaction method, Types of redox reaction- direct and indirect method, Electrochemical cell, Classification of redox reactions.
This document provides information about coordination compounds and Werner's theory of coordination compounds. It begins with an overview of coordination compounds and their importance. It then discusses Werner's theory, including his postulates about primary and secondary valences of metal ions and the coordination number being equal to the number of ligands bound to the metal ion. The document defines key terms related to coordination compounds such as coordination entity, central atom/ion, ligands, coordination number, and isomers. It also discusses nomenclature rules for writing formulas and names of mononuclear coordination compounds. The summary is as follows:
1) The document discusses Werner's pioneering theory of coordination compounds and key postulates about metal ion valences and coordination geometry
1. The document discusses transition metal complexes, including their properties and bonding models.
2. Key topics covered include ligand field theory, isomerism in complexes, naming complexes using IUPAC rules, and the electronic spectra and magnetic properties used to evaluate bonding models.
3. Several bonding models are mentioned, including Werner's theory, Sidgwick's theory, crystal field theory, and ligand field theory.
This document provides information about transition metals and their coordination compounds. It discusses the colors of representative compounds of period 4 transition metals. It also discusses properties of group 6B elements chromium, molybdenum, and tungsten. The document explains that lanthanides have similar properties and most have the electron configuration [Xe]6s24f1-14. It provides examples of coordination compounds and defines coordination number and common geometries of complex ions. Common ligands are identified and the concept of chelates is described. Formulas of coordination compounds are explained and how to determine the charge of the metal ion. The document concludes with descriptions of how to name coordination compounds.
This document discusses complexometric titrations using ethylenediaminetetraacetic acid (EDTA) as the titrant. It describes how EDTA forms stable 1:1 complexes with metal ions and can be used to titrate metals in various ways, including direct titration, back-titration, and replacement titration. It also explains the importance of pH and discusses indicators used for different metal-EDTA complexes. Calcium titrations are discussed as an example, noting how magnesium ions improve the sharpness of the endpoint when using solochrome black indicator.
This document provides an introduction to transition metal complexes. It discusses the aqueous chemistry of metal ions, including hydrolysis. Hexaaqua ions form when transition metals dissolve in water and are surrounded by six water molecules in an octahedral structure. Hydrolysis occurs when water molecules attack these complexes, removing protons and forming hydroxide ions. This makes the solution acidic. The document also discusses stability constants, which are equilibrium constants for the formation of complex ions from their constituent parts. Higher stability constants indicate more stable complexes.
This document discusses coordination compounds and their structures and isomers. It covers Werner's coordination chemistry theories, ligand types including chelating ligands, nomenclature of coordination compounds, and isomerism including geometric and chiral isomers. It also discusses factors that determine coordination numbers and common coordination number structures.
Synthesis, Characterization and Antibacterial Activity of New Complexes of So...IOSR Journals
Complexes of some lanthanide picrates (Ln3+ = Pr3+, Nd3+ and Dy3+) with benzo-18-crown-6 and 221-cryptand were synthesized and characterized by elemental analysis, FTIR, and UV-Visible. Spectrophotometric methods, thermal analysis (TGA & DTG), melting point, magnetic susceptibility and molar conductance. Also an in-vitro study on gram positive (Staphylococcus aureus) and gram negative bacteria (Escherichia coli, Salmonella and pseudomonas aeruginosa) was performed and the results were compared to those of the broad spectrum antibiotic Chloramphinicol. The benzo-18-crown-6 complexes have the general formula of [Ln.L.(Pic)2]Pic.nH2O , where; (Ln3+ = Pr3+, Nd3+, and Dy3+) , (L = Benzo-18-crown-6) , (Pic = Picrate anion) , (n = 1-2). In these complexes two picrate anions are coordinated to the metal ion through the phenolic oxygen and oxygen of the ortho nitro group, thus, the metal ions in these complexes have a coordination number of (10). The complexes of 221-cryptand have the general formula of [Ln.L.(Pic)]Pic2.nH2O where; (Ln3+ = Pr3+, Nd3+, and Dy3+), (L = 221-cryptand), (Pic = Picrate anion), (n = 1,2 or 7). In these complexes one picrate anion is coordinated to the metal ion, also through the phenolic oxygen and the oxygen from the ortho nitro group, thus the metal ions in the cryptand complexes have a coordination number of (9).
Synthesis, Spectroscopic Studies and Antibacterial Activity of Novel Schiff B...IRJET Journal
The document describes the synthesis and characterization of novel Schiff base metal complexes derived from condensation of 5-bromosalicylaldehyde, 4,5-dichloro-o-phenylenediamine, and pentane-2,4-dione. Specifically, copper(II), nickel(II), and oxovanadium(IV) complexes were synthesized and characterized using analytical, spectral, electrochemical, and antimicrobial methods. The complexes were found to have general formula [M(L)]X where M is the metal and L is the tetradentate Schiff base ligand. Spectroscopic data indicated the ligand coordinates through the hydroxyl oxygen and azomethine nitrogen. The metal complexes
IRJET- Equilibrium Studies on Ternary Metal Complexes of Drug Ethambutol Hydr...IRJET Journal
This document discusses the equilibrium studies of ternary metal complexes formed between transition metal ions (nickel and cobalt), the drug ethambutol hydrochloride, and four amino acids (serine, valine, methionine, and glutamic acid). The stability constants of the binary and ternary complexes were determined using pH-metric titration methods. The results showed that the stability of the ternary complexes was higher than the corresponding binary complexes, as indicated by preferential formation and positive relative stability parameters. Specifically, cobalt complexes with serine and nickel complexes with glutamic acid had the highest stability constants among the ternary systems studied.
Research Paper Presentation by Ariful IslamArifulIslam665
The document summarizes a research presentation on the synthesis and characterization of new zinc, copper, and nickel complexes based on an imine ligand containing a 2-aminothiophenol moiety. Specifically, it describes the synthesis of a tridentate Schiff base ligand and its dimeric complexes with zinc, copper, and nickel ions. It then discusses the various techniques used to characterize the ligand and complexes, including IR spectroscopy, UV-Vis spectroscopy, NMR spectroscopy, conductivity measurements, computational modeling, and X-ray crystallography. The key findings are that the complexes were stable in solid and solution states, with the ligand acting as a tridentate chelating agent, and DFT calculations provided insights into their frontier
Synthesis and identification of nickel (ll) , cobalt (ll) and copper (ll) com...Alexander Decker
1. The document describes the synthesis and characterization of nickel(II), cobalt(II), and copper(II) complexes using sodium-1-amino-9,10-dioxo-4-phenylaminanthracene-2-sulphonate (AB25) as a ligand.
2. The complexes were characterized using techniques like elemental analysis, IR and UV-Vis spectroscopy. Nickel(II) complex was found to be diamagnetic while cobalt(II) and copper(II) complexes were paramagnetic.
3. Based on molar ratio and spectral data, the complexes were determined to have the following formulas: nickel(II) and copper(II) complexes were
Synthesis and identification of nickel (ll) , cobalt (ll) and copper (ll) com...Alexander Decker
1. Nickel(II), cobalt(II), and copper(II) complexes were synthesized using sodium-1-amino-9,10-dioxo-4-phenylamin anthracene-2-sulphonate (acid blue 25) as a ligand.
2. The complexes were characterized using techniques like elemental analysis, IR spectroscopy, and UV-VIS spectroscopy. Their physical properties like electrical conductivity and magnetic properties were also determined.
3. Nickel(II) complex was found to be diamagnetic while cobalt(II) and copper(II) complexes were paramagnetic. Cobalt complex did not conduct electricity while the ligand, nickel(II) complex, and copper(
Inhibitive properties, thermodynamic, kinetics and quantum
chemical calculations of polydentate Schiff base compounds
as corrosion inhibitors for iron in acidic and alkaline media
Inhibitive properties, thermodynamic, kinetics and quantumAl Baha University
Inhibitive properties, thermodynamic, kinetics and quantum
chemical calculations of polydentate Schiff base compounds
as corrosion inhibitors for iron in acidic and alkaline media
This document discusses an experimental study on the corrosion inhibition properties of five polydentate Schiff base compounds for iron in acidic and alkaline media. Quantum chemical calculations based on density functional theory were performed to analyze the inhibitor/surface mechanism and experimental data. Weight loss, thermometric, and potentiodynamic polarization measurements showed that the compounds acted as mixed-type inhibitors in nitric acid and cathodic inhibitors in sodium hydroxide. Compound PSC_1 exhibited the highest inhibition efficiency of 78.4% at 10-4M in nitric acid. Adsorption of the inhibitors was found to be spontaneous, exothermic, and obeyed the Temkin isotherm. The quantum calculations aimed to describe the structural nature of
This document discusses an experimental study on the corrosion inhibition properties of five polydentate Schiff base compounds for iron in acidic and alkaline media. Quantum chemical calculations based on density functional theory were performed to analyze the inhibitor/surface mechanism and experimental data. Weight loss, thermometric, and potentiodynamic polarization measurements showed that the compounds acted as mixed-type inhibitors in nitric acid and cathodic inhibitors in sodium hydroxide. Compound PSC_1 exhibited the highest inhibition efficiency of 78.4% at 10-4M in nitric acid. Adsorption of the inhibitors was found to be spontaneous, exothermic, and obeyed the Temkin isotherm. The quantum calculations aimed to describe the structural nature of
This document discusses an experimental study on the inhibitive properties of five polydentate Schiff base compounds as corrosion inhibitors for iron in acidic and alkaline media. Weight loss, thermometric, and potentiodynamic polarization measurements were used to evaluate the inhibition efficiency of the compounds. Quantum chemical calculations based on density functional theory were also performed to analyze the inhibitor/surface interaction mechanism and understand the relationship between molecular structure and inhibition efficiency. The results showed that compound PSC_1 had the best inhibition efficiency of 78.4% at 10-4M concentration in nitric acid solution. Adsorption of the inhibitors was found to be spontaneous, exothermic and obeyed the Temkin isotherm.
IRJET- Effect of Temperature on Stability Constants of Transition Metal C...IRJET Journal
This document discusses a study on the effect of temperature on stability constants of transition metal complexes with the drug ethambutol hydrochloride. Proton ligand stability constants (pKa) and metal ligand stability constants (LogK) were determined for Co(II), Ni(II), Cu(II) and Zn(II) complexes at 300K, 310K, and 320K using pH metric titration methods. The LogK values decreased with increasing temperature, indicating complex formation is exothermic. Negative thermodynamic parameter values (ΔG, ΔH, ΔS) showed complex formation is spontaneous and exothermic. The Cu(II) complexes showed the highest stability based on logβ values, likely due to the
- The document reports on the synthesis and characterization of Schiff base ligands derived from L-valine and their Cu(II), Ni(II), and Co(II) complexes.
- Spectroscopic data revealed that the ligands bind as tridentate in the Cu(II) and Ni(II) complexes and bidentate in the Co(II) complex.
- Magnetic susceptibility measurements showed the complexes have a bimetallic structure with antiferromagnetic interactions.
- Antimicrobial testing found the metal complexes to have greater activity than the free ligand, with the Co(II) complex exhibiting the strongest effects.
This document summarizes research on using fatty acid metallic salts as environmentally friendly herbicides. Specifically, it investigates using potassium laurate and potassium myristate to control the weed Parthenium hysterophorous and the moss Indian moss. The document describes how the metallic salts were prepared and characterized using infrared spectroscopy and conductivity measurements. It found that conductivity increased with concentration due to ionization and micelle formation. Concentration-mortality curves showed the critical micelle concentrations for the salts. Field tests then demonstrated that weekly applications of the salts controlled the target weed and moss.
Multiple Equilibria and Chemical Distribution of Some Bio Metals With β-Amide...IOSR Journals
Abstract: Solution Chemistry of some bivalent metal ions (viz. CoII , NiII ,CuII ,ZnII ) with β-amide α-aminosuccinate (Asparagine)/ α-aminoisoverate( Valine ) (A) and 5-methyl 2,4- dioxopyrimidine ( Thymine ) (B)ligands have been analyzed. Formation constant of quaternary metal complexes and complexation equilibria at 30±1ºC and at constant ionic strength (I=0.1M NaNO3 ) have been explored potentiometrically. Formation of quaternary species in addition to hydroxyl, protonated, binary and ternary species have been reported. Overall formation constant have been evaluated using SCOGS computer program.Species distribution curves of complexes have been plotted as a function of pH to visualize the equlibria system and was refined using ORIGIN program.The metal ligand formation constant of MA,MB,MAB and M1M2AB type of complexes follow Irving William order. The order of stability constants of quaternary systems have been observed as: Cu – Ni > Cu –Zn > Cu–Co > Ni – Zn > Ni – Co > Co –Zn. Solution structures of metal complexes with said ligands have been compared and discussed.
The document summarizes the synthesis and characterization of a binuclear Schiff base ligand and its metal complexes with Cu(II), Ni(II), and VO(IV). The ligand was synthesized by reacting 5-bromo-3-fluorosalicylaldehyde and benzidine. The complexes were prepared by reacting the ligand with metal salts. The ligand and complexes were characterized using elemental analysis, IR, NMR, UV-Vis, magnetic susceptibility, and thermal analysis. The ligand behaves as a tetradentate ligand, coordinating through the azomethine nitrogen and deprotonated phenolic oxygen atoms. The complexes exhibit square planar and square pyramidal geometries. Antimicrobial tests found the compounds
This document examines using voltammetric measurements and rhenium complexes to selectively detect anions. It discusses:
1) Developing anion-sensing systems using rhenium complexes, which can selectively bind anions through electrostatic and covalent interactions.
2) Testing a rhenium complex compound via cyclic voltammetry to see if specific anions can be detected electrochemically.
3) If detected, producing ion-selective electrodes by attaching the complex to electrode surfaces, potentially enabling greater sensor sensitivity and selectivity.
Biosorption process for removal and recovery (1)sonumehta217
This document summarizes a presentation on the biosorption process for removal and recovery of heavy and precious metals from aqueous solutions. The presentation covers the historical background of biosorption from the 1980s to present, current developments including applications and mechanisms, and future trends. Biosorption utilizes inactive biomass such as algae, fungi and bacteria or their derivatives to bind and concentrate metals from dilute solutions. The presentation provides examples of marine algae collected in Singapore that are effective biosorbents and discusses characterization techniques. Mechanisms of metal biosorption include surface complex formation, ion exchange and coordination. Kinetic models of biosorption by various seaweeds and a calcium alginate biosorbent resin are also presented.
This document discusses a study on the inhibitive properties and quantum chemical analysis of 1,4-benzothiazine derivatives for corrosion inhibition of mild steel in acidic medium. Two derivatives, compounds P3 and P4, were synthesized and their structures were confirmed through various analytical techniques. Electrochemical tests including polarization, electrochemical impedance spectroscopy, and weight loss measurements were used to evaluate the corrosion inhibition efficiency of P3 and P4 in 1 M HCl solution. Quantum chemical calculations based on density functional theory were also performed to correlate inhibition efficiency with molecular properties. The results showed that P3 and P4 acted as efficient corrosion inhibitors for mild steel in acidic solution, with inhibition efficiency increasing with increasing concentration. Adsorption
This document discusses solvent extraction, which is a versatile separation method used in analytical chemistry. It can be used to separate, purify, enrich, and analyze both tracer and macro amounts of metal ions. The key principles discussed include the phase rule, which describes solvent extraction as a two-phase system, and the Nernst distribution law, which defines the partition or distribution coefficient. Different types of extraction systems are classified, including chelate extraction involving complex formation, extraction by solvation, and ion-pair formation. Factors that affect metal complex stability such as ligand basicity and ring size are also outlined.
Similar to Dinkars metals ppt-8121 Study gene metal-ligand stability constant of cefadroxil with cu2+ metal ion ph metrically at 0.1 m ionic strength (20)
ESR spectroscopy in liquid food and beverages.pptxPRIYANKA PATEL
With increasing population, people need to rely on packaged food stuffs. Packaging of food materials requires the preservation of food. There are various methods for the treatment of food to preserve them and irradiation treatment of food is one of them. It is the most common and the most harmless method for the food preservation as it does not alter the necessary micronutrients of food materials. Although irradiated food doesn’t cause any harm to the human health but still the quality assessment of food is required to provide consumers with necessary information about the food. ESR spectroscopy is the most sophisticated way to investigate the quality of the food and the free radicals induced during the processing of the food. ESR spin trapping technique is useful for the detection of highly unstable radicals in the food. The antioxidant capability of liquid food and beverages in mainly performed by spin trapping technique.
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
Current Ms word generated power point presentation covers major details about the micronuclei test. It's significance and assays to conduct it. It is used to detect the micronuclei formation inside the cells of nearly every multicellular organism. It's formation takes place during chromosomal sepration at metaphase.
Phenomics assisted breeding in crop improvementIshaGoswami9
As the population is increasing and will reach about 9 billion upto 2050. Also due to climate change, it is difficult to meet the food requirement of such a large population. Facing the challenges presented by resource shortages, climate
change, and increasing global population, crop yield and quality need to be improved in a sustainable way over the coming decades. Genetic improvement by breeding is the best way to increase crop productivity. With the rapid progression of functional
genomics, an increasing number of crop genomes have been sequenced and dozens of genes influencing key agronomic traits have been identified. However, current genome sequence information has not been adequately exploited for understanding
the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
high-throughput phenotyping has become the major bottleneck restricting crop breeding. Plant phenomics has been defined as the high-throughput, accurate acquisition and analysis of multi-dimensional phenotypes
during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
EWOCS-I: The catalog of X-ray sources in Westerlund 1 from the Extended Weste...Sérgio Sacani
Context. With a mass exceeding several 104 M⊙ and a rich and dense population of massive stars, supermassive young star clusters
represent the most massive star-forming environment that is dominated by the feedback from massive stars and gravitational interactions
among stars.
Aims. In this paper we present the Extended Westerlund 1 and 2 Open Clusters Survey (EWOCS) project, which aims to investigate
the influence of the starburst environment on the formation of stars and planets, and on the evolution of both low and high mass stars.
The primary targets of this project are Westerlund 1 and 2, the closest supermassive star clusters to the Sun.
Methods. The project is based primarily on recent observations conducted with the Chandra and JWST observatories. Specifically,
the Chandra survey of Westerlund 1 consists of 36 new ACIS-I observations, nearly co-pointed, for a total exposure time of 1 Msec.
Additionally, we included 8 archival Chandra/ACIS-S observations. This paper presents the resulting catalog of X-ray sources within
and around Westerlund 1. Sources were detected by combining various existing methods, and photon extraction and source validation
were carried out using the ACIS-Extract software.
Results. The EWOCS X-ray catalog comprises 5963 validated sources out of the 9420 initially provided to ACIS-Extract, reaching a
photon flux threshold of approximately 2 × 10−8 photons cm−2
s
−1
. The X-ray sources exhibit a highly concentrated spatial distribution,
with 1075 sources located within the central 1 arcmin. We have successfully detected X-ray emissions from 126 out of the 166 known
massive stars of the cluster, and we have collected over 71 000 photons from the magnetar CXO J164710.20-455217.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/
Or: Beyond linear.
Abstract: Equivariant neural networks are neural networks that incorporate symmetries. The nonlinear activation functions in these networks result in interesting nonlinear equivariant maps between simple representations, and motivate the key player of this talk: piecewise linear representation theory.
Disclaimer: No one is perfect, so please mind that there might be mistakes and typos.
dtubbenhauer@gmail.com
Corrected slides: dtubbenhauer.com/talks.html
hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
The binding of cosmological structures by massless topological defectsSérgio Sacani
Assuming spherical symmetry and weak field, it is shown that if one solves the Poisson equation or the Einstein field
equations sourced by a topological defect, i.e. a singularity of a very specific form, the result is a localized gravitational
field capable of driving flat rotation (i.e. Keplerian circular orbits at a constant speed for all radii) of test masses on a thin
spherical shell without any underlying mass. Moreover, a large-scale structure which exploits this solution by assembling
concentrically a number of such topological defects can establish a flat stellar or galactic rotation curve, and can also deflect
light in the same manner as an equipotential (isothermal) sphere. Thus, the need for dark matter or modified gravity theory is
mitigated, at least in part.
2. Coordination chemistry is the branch of chemistry, which lets us know how
metal complexes are built. A complex is a cluster of ions and molecules, which
can exists independently but prefers to join together in a structurally well
defined manner. A metal complex consists of a metal ion, often structurally
well-defined manner. A metal complex consists of a metal ion, often referred to
as the central metal atom or ion, which binds a number of ions and or
molecules, called ligand.
The reorganization of true nature of complexes began with
Alfred Warner, who in 1893 proposed what is now commonly referred to as
Warner’s coordination theory He prepared an characterized hundreds of
coordination compounds. For this major contribution, Warner awarded the
noble prize in chemistry in 1913.
3. The interaction of transition metal ions with biological molecules provides one of
the fascinating areas of coordination chemistry.
The application has been grown readily due to their wide range in household,
industry, medicine, chemical and biological system. Some of the important once
are
Plant growth:
Plants need various nutrients for healthy growth. Essential nutrients
include number of mental such as iron, copper and zinc etc. Iron in the +3 state
the soil is mostly hydrolyzed to from insoluble iron hydroxide, which cannot be
taken up by plants. Deficient in iron are likely to develop a disorder known as
iron chlorosis, evidenced by yellowing leaves.
• Therapeutic chelating agents:
The coordination complex of platinum effectively inhibit the growth of cancerous cells.
It has long been suspected that chelation processes are associated both with the
development of cancer and with antitumor actively
4. Important of cefadroxil
Cefadroxil is a broad – spectrum antibiotic of the cephalic sporum HPE Effectixe in
gram positive and gram negative bacterial infection. It is a bactericidal
antibiotic.Cefadroxil is a first generation cephalosporin antibacterial ative of cefadraxil.It
has been effectiom of the skin and urinary fract.
Pharmacakinetics:-cefadroxil is almost completely absorded from gastrointestinal
tract after does of 500 mg and 19 by mouth, peak plasma doncetration of about 16 and
30 micrograms/ ml are bastioned after 1.5 to 2 hours.
It is widely distributed to body tissue and fluid it crosses the placentas and appears in
breast milk.
5. Side effect :- toast common side effect cefadroxil is diarrhea, nausea,
upset stomach and vomiting other rahshes hixes, itching .
Dental use :- is used as antibiotic prophylaxis dental pracedare fpr patiens
allergic to penicillin.
Veterinary use :- Canbe used for treating interacted woinds on animals
usuallyin powder from mixied with water has a colorand smell similar amount
dependent on their we igth and severity of intercting.
6. General Methods to Study Metal Complexes:
The numbers of methods deal with the study of metal –ligand complexes in
solution are
,
pH Metric Technique-
Metal complex formation may be taken place due to the displacement of
proton from ligand causing a drop in the pH- metric value of the solution. Irving and Rossotti
61 have given a method for calculation of stability constants of complexes by pH-metric
technique. This general technique has been followed by Calvin and bjerrum.
Co-relation between the basicity of the ligand and stability of complexes:
The complex formation is a complexation between metal ions and protons in
most cases. Therefore, it is reasonable to expect that there is some correlation between the
stability constant of the complex and the acidic dissociation constant of conjugate acid of the
ligand.Larsson" finds linear relationships between the corresponding constants for the
complexes of silver ion with organic amines. Subsequently similar correlations were found in
many complex systems". The ligand may affect the chelating tendency in two possible ways.
•It may influence of basicity of donor group by inductive and resonance effect.
•The addition of groups on the ligand may be purely statistical. Sterical effects prevent the
ligand ions or molecules from acquiring the orientation about the central metal ion most
favourable for chelation.
7. Determination of the stability constants from the experimental data consist
of three steps:-
The determination of the formation curve of the system expressed as a Plot
•The calculation of values of log K1 and log 2 by solving the formation
of the system.
n
-
n
-
n
-
-------------- (16)against log K = log 1
[L]
•The calculation of values of log K1 and log K2 by solving the formation
of the system.
• The conversion of stoichiomctric constants into the thermodynamic
functions
The experimental procedure involves titration of:
•Nitric Acid (A)
•Nitric Acid -1- Ligand Acid (A + L)
•Nitric Acid * Ligand Acid + Metal Salt (A — L + hi)
With standard solution of sodium hydroxide. The ionic strength of each
solution is kept constant at 0.01 M by addition of 1.00 potassium nitrate
solution
8. Calculation of A, n and pL
n
-
A
= y -
(V2 - V1) (N + E0)
(V
0
+ V1 ) T
0 L
1)The experimental data obtained from the titration curves helps in calculation of nA n
and pL.i) Proton ligand formation number nA for different pH values can be obtained from
expression.
2)The metal ligand formation number n can be calculated from the
expression:-
=
9. Chapter – III
EXPERIMENTAL, RESULTS AND DISCUSSION
ExperimentalSolvents
Distilled Water:
Distilled water prepared may contain small quantities of dissolved ammonia and carbon
dioxide.Distilled water used investigation was obtained by redistilling twice the distilled water
prepared from alkaline potassium permanganate: the head and tail fractions were rejected to
remove the dissolved ammonia'`. The dissolution of carbondioxide was prevented during
distillation by connecting a potassium hydroxide trap in the receiver of distillate. The resulting
distillate was boiled to expel oxygen and then it was cooled in a well-stoppered glass bottle
(Distilled water free from ammonia and carbondioxide had pH 7.00)
Sodium Hydroxide:
The solution of sodium hydroxide {E. Merck} was prepared carbonate by allowing the
solution to stand for along time till any if present precipitated. The solution was filtered
through a sintered glass crucible and kept in a pyrex veasel free from carbondioxide and
was used as the titrant for the pH-metric titrations. Titrating against standard oxalic acid
solution before starting an experiment standardized the solution of sodium hydroxid.
10. Formation Curves –
The formation curves were constructed by plotting the values of
Aagainst pH of solution and are presented in Fig. 19 to 34. The dissociation constant pk of
ligands are calculated from formation curves. The values of pk obtained are represented in Table
34(a). The dissociation constants (pk values) for substituted ligands are found to be above pH
10.00 for all the systems.
Meta I-Ligand Stability Constants –
The metal Ligand stability constant is the association or formation constant. For the conversion of
any Calvin-Bjerrum titrations data -into stability constants, following conditions should hold
good for the system under investigation.
•Formation of complex or chelate under the experimental conditions Employed.
•Absence of metal ion hydrolysis, polynuclear hydrogen and hydroxyl complexes and anion of
complexing metal ions.
11. System log log
Cu (II) ligand 1.29 0.386
Metal-Ligand stability constant
Conclusion
•The departure between acid curve and ligand curve indicated the dissociation of phenolic. -OH
group.
•The departure between ligand curve and metal curve indicated the commencement of complex
formation.
•The change in colour during pH-metric titration also indicated the fomution of complexes
between ligands and metal ions.
The values of pK and log K arc increased with increasing the mixture of water which is attributed
due to the effect of bulky solvent.
•The non-linear relationship for the graphs I:D versus pK/log K but linear relation
relationship for the graphs between mole fraction versus pK/log K is observed.
18. Reference:
• http:// www.tku-e.com/assets/MIC/cefadroxil.pdf
• cefadroxil side effect,” Drugs
• begrouthy R, Robin, F, Dabboussi, F, Mallat, H, Hamze , M, Bonnet, R.
• Pristinnamyun :- old drug, new tricks?
Cooper, E. C Curtis, N, Cranswick, N Gwee, A.
• Isolation of ciprofloxacin – resistant legionella pneumophila in a patient with severe pneumonia. Bruin, J.P.,
koshkolda, Ijzerm an, E.P.F Luck, C Diederen, B.M.W. den boer, J.W, Mouton, J.W.
• Genomic identification of ahovel cotrimoxazole resistance genotype and its prevalence amongst streptococeus
pneumonia in malawin
Author: - Cornick J.E. Etal: Source- joirna antimicrobial chemotherapy.
• Game changex – antibiotic and other in works for superbug
Author: - Dolgin E
Source: - Nature Taedicine
• Towards new business model for R and D for novel antibiotics.
Author: - So A.D. Etal:
Source: - Drug Resistance update
• Psychology, Health and medicines
Author: - Bell B.G. Etal :
• BMC infectious Diseases
Author:- Bell Bg Etal :
• Kinetic and mechanism of oxidation of giutamio Acid by N- Bromoph – thalimide in Aqueous Acidc. Medium
N. M. I. Alhaji , S. Sofiya Lawre