Tungsten Hexachloride
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Tungsten Hexachloride
Tungsten hexachloride is the chemical compound of tungsten and chlorine with the formula WCl6. This dark violet blue species exists as a volatile solid under standard conditions. It is an important starting reagent in the preparation of tungsten compounds. Other examples of charge-neutral hexachlorides are rhenium(VI) chloride and molybdenum(VI) chloride. The highly volatile tungsten hexafluoride is also known. As a d0 ion, W(VI) forms diamagnetic derivatives. The hexachloride is octahedral with equivalent W–Cl distances of 2.24–2.26 Å. Preparation Tungsten hexachloride can be prepared by chlorinating tungsten metal in a sealed tube at 600 °C: : W + 3 Cl2 → WCl6 Properties and Reactions Tungsten (VI) chloride is a blue-black solid at room temperature. At lower temperatures, it becomes wine-red in color. A red form of the compound can be made by rapidly condensing its vapor, which reverts to the blue-black form on gentle heating. It is readily hydrolyzed, even ...
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Debye
The debye (symbol: D) (; ) is a CGS unit (a non- SI metric unit) of electric dipole momentTwo equal and opposite charges separated by some distance constitute an electric dipole. This dipole possesses an electric dipole moment whose value is given as charge times length of separation, it is a vector whose direction is in the direction of the unit vector of the position vector of the positive charge w.r.t negative charge: :p = ''q''r. named in honour of the physicist Peter J. W. Debye. It is defined as statcoulomb-centimeters.The statcoulomb is also known as the franklin or electrostatic unit of charge. :1 statC = 1 Fr = 1 esu = 1 cm3/2⋅g1/2⋅s−1. Historically the debye was defined as the dipole moment resulting from two charges of opposite sign but an equal magnitude of 10−10 statcoulomb10−10 statcoulomb corresponds to approximately 0.2083 units of elementary charge. (generally called e.s.u. (electrostatic unit) in older scienti ...
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Tungsten Oxychloride
Tungsten dichloride dioxide, or Tungstyl chloride is the chemical compound with the formula W O2 Cl2. It is a yellow-colored solid. It is used as a precursor to other tungsten compounds. Like other tungsten halides, WO2Cl2 is sensitive to moisture, undergoing hydrolysis. Preparation WO2Cl2 is prepared by ligand redistribution reaction from tungsten trioxide and tungsten hexachloride: : 2 WO3 + WCl6 → 3 WO2Cl2 Using a two-zone tube furnace, a vacuum-sealed tube containing these solids is heated to 350 °C. The yellow product sublimes to the cooler end of the reaction tube. No redox occurs in this process. An alternative route highlights the oxophilicity of tungsten: :WCl6 + 2 O(Si(CH3)3)2 → 3 WO2Cl2 + 4 ClSi(CH3)3 This reaction, like the preceding one, proceeds via the intermediacy of WOCl4. Structure The compound is a polymer consisting of distorted octahedral W centres. The monomer is characterized by two short W-O distances, typical for a multiple W-O b ...
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Tungsten(IV) Chloride
Tungsten(IV) chloride is an inorganic compound with the formula WCl4. It is a diamagnetic black solid. The compound is of interest in research as one of a handful of binary tungsten chlorides. Structure and preparation WCl4 is usually prepared by reduction tungsten hexachloride. Many reductants have been reported, including red phosphorus, tungsten hexacarbonyl, gallium, tin, and antimony. The latter is reported to be optimal: :\mathrm Like most binary metal halides, WCl4 is polymeric. It consists of linear chains of tungsten atoms each in octahedral geometry. Of six chloride ligands attached to each W center, four are bridging ligand In coordination chemistry, a bridging ligand is a ligand that connects two or more atoms, usually metal ions. The ligand may be atomic or polyatomic. Virtually all complex organic compounds can serve as bridging ligands, so the term is usually ...s. The W-W separations are alternatingly bonding (2.688 Å) and nonbonding (3.787 Å). ...
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Tungsten(V) Chloride
Tungsten(V) chloride is an inorganic compound with the formula W2 Cl10. This compound is analogous in many ways to the more familiar molybdenum pentachloride. The material is prepared by reduction of tungsten hexachloride. One method involves the use of tetrachloroethylene as the reductant :2 WCl6 + C2Cl4 → W2Cl10 + C2Cl6 The blue green solid is volatile under vacuum and slightly soluble in nonpolar solvents. The compound is oxophilic Oxophilicity is the tendency of certain chemical compounds to form oxides by hydrolysis or abstraction of an oxygen atom from another molecule, often from organic compounds. The term is often used to describe metal centers, commonly the early trans ... and is highly reactive toward Lewis bases. Structure The compound exists as a dimer, with a pair of octahedral tungsten(V) centres bridged by two chloride ligands. The W---W separation is 3.814 Å, which is non-bonding. The compound is isostructural with Nb2Cl10 and Mo2Cl10. The com ...
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Alkoxide
In chemistry, an alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom. They are written as , where R is the organic substituent. Alkoxides are strong bases and, when R is not bulky, good nucleophiles and good ligands. Alkoxides, although generally not stable in protic solvents such as water, occur widely as intermediates in various reactions, including the Williamson ether synthesis. Transition metal alkoxides are widely used for coatings and as catalysts. Enolates are unsaturated alkoxides derived by deprotonation of a bond adjacent to a ketone or aldehyde. The nucleophilic center for simple alkoxides is located on the oxygen, whereas the nucleophilic site on enolates is delocalized onto both carbon and oxygen sites. Ynolates are also unsaturated alkoxides derived from acetylenic alcohols. Phenoxides are close relatives of the alkoxides, in which the alkyl group is replaced by a derivative ...
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Thiocyanate
Thiocyanate (also known as rhodanide) is the anion . It is the conjugate base of thiocyanic acid. Common derivatives include the colourless salts potassium thiocyanate and sodium thiocyanate. Mercury(II) thiocyanate was formerly used in pyrotechnics. Thiocyanate is analogous to the cyanate ion, , wherein oxygen is replaced by sulfur. is one of the pseudohalides, due to the similarity of its reactions to that of halide ions. Thiocyanate used to be known as rhodanide (from a Greek word for rose) because of the red colour of its complexes with iron. Thiocyanate is produced by the reaction of elemental sulfur or thiosulfate with cyanide: : 8 CN- + S8 -> 8 SCN- : CN- + S2O3^2- -> SCN- + SO3^2- The second reaction is catalyzed by thiosulfate sulfurtransferase, a hepatic mitochondrial enzyme, and by other sulfur transferases, which together are responsible for around 80% of cyanide metabolism in the body. Biological chemistry of thiocyanate in medicine Thiocyanate is known to ...
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Bromide
A bromide ion is the negatively charged form (Br−) of the element bromine, a member of the halogens group on the periodic table. Most bromides are colorless. Bromides have many practical roles, being found in anticonvulsants, flame-retardant materials, and cell stains. Although uncommon, chronic toxicity from bromide can result in bromism, a syndrome with multiple neurological symptoms. Bromide toxicity can also cause a type of skin eruption, see potassium bromide. The bromide ion has an ionic radius of 196 pm. Natural occurrence Bromide is present in typical seawater (35  PSU) with a concentration of around 65 mg/L, which is about 0.2% of all dissolved salts. Seafood and deep sea plants generally have higher levels than land-derived foods. Bromargyrite—natural, crystalline silver bromide—is the most common bromide mineral known but is still very rare. In addition to silver, bromine is also in minerals combined with mercury and copper. Formation and re ...
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Epoxide
In organic chemistry, an epoxide is a cyclic ether () with a three-atom ring. This ring approximates an equilateral triangle, which makes it strained, and hence highly reactive, more so than other ethers. They are produced on a large scale for many applications. In general, low molecular weight epoxides are colourless and nonpolar, and often volatile. Nomenclature A compound containing the epoxide functional group can be called an epoxy, epoxide, oxirane, and ethoxyline. Simple epoxides are often referred to as oxides. Thus, the epoxide of ethylene (C2H4) is ethylene oxide (C2H4O). Many compounds have trivial names; for instance, ethylene oxide is called "oxirane". Some names emphasize the presence of the epoxide functional group, as in the compound ''1,2-epoxyheptane'', which can also be called ''1,2-heptene oxide''. A polymer formed from epoxide precursors is called an ''epoxy'', but such materials do not contain epoxide groups (or contain only a few residual epoxy ...
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Butyl Lithium
Butyllithium may refer to one of 5 isomeric organolithium reagents of which 3 are commonly used in chemical synthesis: * ''n''-Butyllithium, abbreviated BuLi or nBuLi * ''sec''-Butyllithium, abbreviated ''sec''-BuLi or sBuLi, has 2 stereoisomers, but is commonly used as racemate *isobutyllithium * ''tert''-Butyllithium, abbreviated ''tert''-BuLi or tBuLi {{Chemistry index ...
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Hexamethyl Tungsten
Hexamethyltungsten is the chemical compound W( CH3)6 also written WMe6. Classified as a transition metal alkyl complex, hexamethyltungsten is an air-sensitive, red, crystalline solid at room temperature; however, it is extremely volatile and sublimes at −30 °C. Owing to its six methyl groups it is extremely soluble in petroleum, aromatic hydrocarbons, ethers, carbon disulfide, and carbon tetrachloride. Synthesis Hexamethyltungsten was first reported in 1973 by Wilkinson and Shortland, who described its preparation by the reaction of methyllithium with tungsten hexachloride in diethyl ether. The synthesis was motivated in part by previous work which indicated that tetrahedral methyl transition metal compounds are thermally unstable, in the hopes that an octahedral methyl compound would prove to be more robust. In 1976, Wilkinson and Galyer disclosed an improved synthesis using trimethylaluminium in conjunction with trimethylamine, instead of methyllithium. The stoichiome ...
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Trimethylaluminium
Trimethylaluminium is one of the simplest examples of an organoaluminium compound. Despite its name it has the formula Al2( CH3)6 (abbreviated as Al2Me6 or TMA), as it exists as a dimer. This colorless liquid is pyrophoric. It is an industrially important compound, closely related to triethylaluminium. Structure and bonding The structure and bonding in Al2R6 and diborane are analogous (R = alkyl). In Al2Me6, the Al-C(terminal) and Al-C(bridging) distances are 1.97 and 2.14 Å, respectively. The Al center is tetrahedral. The carbon atoms of the bridging methyl groups are each surrounded by five neighbors: three hydrogen atoms and two aluminium atoms. The methyl groups interchange readily intramolecularly. At higher temperatures, the dimer cracks into monomeric AlMe3. Synthesis TMA is prepared via a two-step process that can be summarized as follows: :2 Al + 6 CH3Cl + 6 Na → Al2(CH3)6 + 6 NaCl Applications Catalysis Starting with the invention of Ziegler-Natta catalysis, ...
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Phosphorus Oxychloride
Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula . It hydrolyses in moist air releasing phosphoric acid and fumes of hydrogen chloride. It is manufactured industrially on a large scale from phosphorus trichloride and oxygen or phosphorus pentoxide. It is mainly used to make phosphate esters such as tricresyl phosphate. Structure Like phosphate, is tetrahedral in shape. It features three P−Cl bonds and one strong P=O double bond, with an estimated bond dissociation energy of 533.5 kJ/mol. On the basis of bond length and electronegativity, the Schomaker-Stevenson rule suggests that the double bond form is dominant, in contrast with the case of . The P=O bond involves the donation of the lone pair electrons on oxygen ''p''-orbitals to the antibonding combinations associated with phosphorus-chlorine bonds, thus constituting ''π'' bonding. Phosphoryl chloride exists as neutral molecules in the solid, liquid and ...
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