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Transition Metal Complexes Of 1,10-phenanthroline
Transition metal complexes of 1,10-phenanthroline ("phen") are coordination complexes containing one or more 1,10-phenanthroline ligands. Complexes have been described for many transition metals. In almost all complexes, phen serves as a bidentate ligand, binding metal centers with the two nitrogen atoms. Examples include PtCl2(phen) and e(phen)3sup>2+. Homoleptic complexes Several homoleptic complexes are known of the type (phen)3sup>2+. Particularly well studied is e(phen)3sup>2+, called "ferroin." It can be used for the photometric determination of Fe(II). It is used as a redox indicator with standard potential +1.06 V. The reduced ferrous form has a deep red colour and the oxidised form is light-blue. The pink complex i(phen)3sup>2+ has been resolved into its Δ and Λ isomers. Both e(phen)3sup>2+ and e(phen)3sup>3+ have been resolved into optical isomers. Copper(I) forms u(phen)2sup>+, which is luminescent. Bioinorganic chemistry It has long been known t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
CSD CIF JEXXEQ
CSD may refer to: Finance * Central securities depository * Confederate States Dollar * Serbian dinar, by previous ISO 4217 code Organizations Education * California School for the Deaf (other), several institutions * Canyons School District, in Utah, US * Cheltenham School District, in Pennsylvania, US * Christina School District, in Delaware, US * Cleveland School District, in Mississippi, US * Cordova School District, in Alaska, US Other organizations * Canteen Stores Department (India), a chain of stores operated by the Indian Ministry of Defence at military bases * CSD Pakistan (Canteen Stores Department), a chain of stores operated by the Pakistani Ministry of Defence * Chartered Society of Designers, a British learned society for various kinds of design work * Commission on Sustainable Development (1992–2013), a former UN agency * Communication Service for the Deaf, an American non-profit company providing ASL services * Congress of Democratic Trade Unions ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Enzyme Inhibitor
An enzyme inhibitor is a molecule that binds to an enzyme and blocks its Enzyme activity, activity. Enzymes are proteins that speed up chemical reactions necessary for life, in which Substrate (biochemistry), substrate molecules are converted into Product (chemistry), products. An enzyme Enzyme catalysis, facilitates a specific chemical reaction by binding the substrate to its active site, a specialized area on the enzyme that accelerates the Rate-determining step, most difficult step of the reaction. An enzyme inhibitor stops ("inhibits") this process, either by binding to the enzyme's active site (thus preventing the substrate itself from binding) or by binding to another site on the enzyme such that the enzyme's catalysis of the reaction is blocked. Enzyme inhibitors may bind Reversible reaction, reversibly or irreversibly. Irreversible inhibitors form a Covalent bond, chemical bond with the enzyme such that the enzyme is inhibited until the chemical bond is broken. By cont ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,2-Benzoquinone
1,2-Benzoquinone, also called ''ortho''-benzoquinone, is an organic compound with formula . It is one of the two isomers of quinone, the other being 1,4-benzoquinone. It is a red volatile solid that is soluble in water and diethyl ether. It is rarely encountered because of its instability, but it is of fundamental interest as the parent compound of many derivatives which are known. Structure The molecule has C symmetry. X-ray crystallography shows that the double bonds are localized, with alternatingly long and short C-C distances within the ring. The C=O distances of 1.21 Å are characteristic of ketones. Preparation and reactions 1,2-Benzoquinone is produced on oxidation of catechol exposed to air in aqueous solution or by ortho oxidation of a phenol. A strain of the bacterium ''Pseudomonas mendocina'' metabolises benzoic acid, yielding 1,2-benzoquinone via catechol. Ortho-quinones are widely used in organic synthesis. Occurrence of ''ortho''-quinones 4,5-Dimethyl-1,2-ben ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,10-Phenanthroline-5,6-dione
1,10-Phenanthroline-5,6-dione is an organic compound with the formula . It is the quinone derivative of 1,10-phenanthroline. The compound exhibits many reactions, including condensations with diamines to give quinoxalines and decarbonylation to give a diazafluorenone. The compound is prepared by oxidation of 1,10-phenanthroline with a mixture of nitric and sulfuric acid Sulfuric acid (American spelling and the preferred IUPAC name) or sulphuric acid (English in the Commonwealth of Nations, Commonwealth spelling), known in antiquity as oil of vitriol, is a mineral acid composed of the elements sulfur, oxygen, ...s. 5-Nitro-1,10-phenanthroline is an intermediate. See also * Phanquinone References {{DEFAULTSORT:Phenanthroline-5,6-dione, 1,10- Phenanthrolines Quinones Bipyridines Enones ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bathocuproine
Bathocuproine is an organic compound with the formula . It is related to 1,10-phenanthroline by the placement of two methyl groups and two phenyl groups in the 2,9 and 4,7 positions, respectively. Like 1,10-phenanthroline, bathocuproine is a bidentate chelating ligand In coordination chemistry, a ligand is an ion or molecule with a functional group that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves formal donation of one or more of the ligand's el .... The two methyl groups flank the nitrogen centers, such that bathocuproine is a bulky ligand. It forms a monomeric 1:1 complex with nickel(II) chloride, whereas the less bulky parent phenanthroline forms a 2:1 complex. This compound was first prepared by Case and Brennan in the early 1950s is a pale yellow solid that is soluble in polar organic solvents.{{cite encyclopedia, author=Guosheng Liu, Yichen, Wu, year=2012, title = Encyclopedia of Reagents for Organic S ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phenanthroline Numbering
1,10-Phenanthroline (phen) is a heterocyclic organic compound. It is a white solid that is soluble in organic solvents. The 1,10 refers to the location of the nitrogen atoms that replace CH's in the hydrocarbon called phenanthrene. Abbreviated "phen", or sometimes "o-phen" for ortho-phenanthroline, it is used as a ligand in coordination chemistry, forming strong complexes with most metal ions.Luman, C.R. and Castellano, F.N. (2003) "Phenanthroline Ligands" in Comprehensive Coordination Chemistry II. Elsevier. . It is often sold as the monohydrate. Synthesis Phenanthroline can be prepared by two successive Skraup reactions of glycerol with ''o''-phenylenediamine, catalyzed by sulfuric acid, and an oxidizing agent, traditionally aqueous arsenic acid or nitrobenzene. Dehydration of glycerol gives acrolein which condenses with the amine followed by a cyclization. Reactions Oxidation of 1,10-phenanthroline with a mixture of nitric and sulfuric acids gives 1,10-phenanthroline-5,6-d ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bathocuproine
Bathocuproine is an organic compound with the formula . It is related to 1,10-phenanthroline by the placement of two methyl groups and two phenyl groups in the 2,9 and 4,7 positions, respectively. Like 1,10-phenanthroline, bathocuproine is a bidentate chelating ligand In coordination chemistry, a ligand is an ion or molecule with a functional group that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves formal donation of one or more of the ligand's el .... The two methyl groups flank the nitrogen centers, such that bathocuproine is a bulky ligand. It forms a monomeric 1:1 complex with nickel(II) chloride, whereas the less bulky parent phenanthroline forms a 2:1 complex. This compound was first prepared by Case and Brennan in the early 1950s is a pale yellow solid that is soluble in polar organic solvents.{{cite encyclopedia, author=Guosheng Liu, Yichen, Wu, year=2012, title = Encyclopedia of Reagents for Organic S ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Neocuproine
Neocuproine is a heterocyclic organic compound and chelating agent. Phenanthroline ligands were first published in the late 19th century, and the derivatives substituted at the 2 and 9 positions are among the most studied of the modified phenanthrolines. Synthesis and structure Neocuproine can be prepared by sequential Skraup reactions (Doebner-Miller reaction/condensation) of o-nitroaniline (2-Nitroaniline) with crotonaldehyde diacetate. An alternate synthesis involves the condensation of o-phenylenediamine, m-nitrobenzenesulphonate, and crotonaldehyde diacetate. This method gives higher yields but is less economical. Neocuproine crystallizes as a dihydrate and a hemihydrate. Coordination chemistry In the early 1930s, phenanthroline derivatives became known for their use as colorimetric indicators for many transition metals. Neocuproine proved to be highly selective for copper(I). The resulting complex, [Cu(neocuproine)2]+ has a deep orange-red color. The properties of coppe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tetrahedral Coordination
In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron. The bond angles are arccos(−) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane () as well as its heavier analogues. Methane and other perfectly symmetrical tetrahedral molecules belong to point group ''Td'', but most tetrahedral molecules have lower symmetry. Tetrahedral molecules can be chiral. Tetrahedral bond angle The bond angle for a symmetric tetrahedral molecule such as CH4 may be calculated using the dot product of two vectors. As shown in the diagram at left, the molecule can be inscribed in a cube with the tetravalent atom (e.g. carbon) at the cube centre which is the origin of coordinates, O. The four monovalent atoms (e.g. hydrogens) are at four corners of the cube (A, B, C, D) chosen so that no two atoms are at adjacent corners linked by only one cube edge. If the edge length ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
