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List Of Named Inorganic Compounds
Well-known inorganic and organometallic compounds and reagents that are named after individuals include: * Adams's catalyst (proposed to be PtOx) * Adamsite (NH(C6H4)2AsCl) * Adkins catalyst (Cu2Cr2O5) * Attenburrow's Oxide (MnO2) * Arduengo carbene (class of compounds) * Baeyer's reagent (KMnO4(aq)) * Benedict's reagent * Bobbitt's salt (4-(Acetylamino)-2,2,6,6-tetramethyl-1-oxo-piperidinium tetrafluoroborate) * Bertrand carbene (class of compounds) * Brookhart's acid (H(OEt2)2BArF4) * Buckminsterfullerene (C60) * Burow's solution (Al(CH3CO2)3(aq)) * Calderon catalyst (WCl6/EtAlCl2/EtOH) * Caro's acid (H2SO5) * Chevreul's salt (Cu3(SO3)2 • 2 H2O) * Chugaev's red salt ( t(C(NHMe)2N2H2CNMe)2]Cl2) * Chugaev's salt ( t(NH3)5Cll3) * Cleve's triammine ( t(NH3)3Cll) * Collman's reagent (Na2Fe(CO)4) * Collins reagent (CrO3 / py / CH2Cl2) * Condy's crystals (KMnO4) * Corey–Chaykovsky reagent (O=S(CH2)Me2) * Cornforth reagent ( yHsub>2 r2O7 * Crabtree's catalyst (Ir(CO ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Inorganic Chemistry
Inorganic chemistry deals with synthesis and behavior of inorganic and organometallic compounds. This field covers chemical compounds that are not carbon-based, which are the subjects of organic chemistry. The distinction between the two disciplines is far from absolute, as there is much overlap in the subdiscipline of organometallic chemistry. It has applications in every aspect of the chemical industry, including catalysis, materials science, pigments, surfactants, coatings, medications, fuels, and agriculture. Key concepts Many inorganic compounds are ionic compounds, consisting of cations and anions joined by ionic bonding. Examples of salts (which are ionic compounds) are magnesium chloride MgCl2, which consists of magnesium cations Mg2+ and chloride anions Cl−; or sodium oxide Na2O, which consists of sodium cations Na+ and oxide anions O2−. In any salt, the proportions of the ions are such that the electric charges cancel out, so that the bulk compound is e ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chevreul's Salt
Chevreul's salt (copper(I,II) sulfite dihydrate, Cu2SO3•CuSO3•2H2O or Cu3(SO3)2•2H2O), is a copper salt which was prepared for the first time by a French chemist Michel Eugène Chevreul in 1812. Its unusual property is that it contains copper in both of its common oxidation states. It is insoluble in water and stable in air. What was known as Rogojski's salt is a mixture of Chevreul's salt and metallic copper. Preparation Chevreul's salt is prepared by treating aqueous copper sulfate with a solution of potassium metabisulfite. The solution changes colour from blue to green immediately. The identity of the green species is unknown. Heating this solution produces a reddish solid precipitate: 3 CuSO4 + 4 K2S2O5 + 3 H2O → Cu3(SO3)2•2H2O + 4 K2SO4 + 4 SO2 + H2SO4 When sodium ions are present in the solutions that form the salt, sodium can substitute for some of the copper (I), as the ions have the same charge and similar sizes. Reactions Chevreul's salt exhibits properties ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Fétizon Oxidation
Fétizon oxidation is the oxidation of primary and secondary alcohols utilizing the compound silver(I) carbonate absorbed onto the surface of celite also known as Fétizon's reagent first employed by Marcel Fétizon in 1968. It is a mild reagent, suitable for both acid and base sensitive compounds. Its great reactivity with lactols makes the Fétizon oxidation a useful method to obtain lactones from a diol. The reaction is inhibited significantly by polar groups within the reaction system as well as steric hindrance of the α-hydrogen of the alcohol. Preparation Fétizon's reagent is typically prepared by adding silver nitrate to an aqueous solution of a carbonate, such as sodium carbonate or potassium bicarbonate, while being vigorously stirred in the presence of purified celite. Mechanism A proposed mechanism for the oxidation of an alcohol by Fétizon's reagent involves single electron oxidation of both the alcoholic oxygen and the hydrogen alpha to the alcohol by two atoms of s ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Fenton's Reagent
Fenton's reagent is a solution of hydrogen peroxide (H2O2) with ferrous iron (typically iron(II) sulfate, FeSO4) as a catalyst that is used to oxidize contaminants or waste waters as part of an advanced oxidation process. Fenton's reagent can be used to destroy organic compounds such as trichloroethylene (TCE) and tetrachloroethylene (perchloroethylene, PCE). It was developed in the 1890s by Henry John Horstman Fenton as an analytical reagent. Overview Iron(II) is oxidized by hydrogen peroxide to iron(III), forming a hydroxyl radical and a hydroxide ion in the process. Iron(III) is then reduced back to iron(II) by another molecule of hydrogen peroxide, forming a hydroperoxyl radical and a proton. The net effect is a disproportionation of hydrogen peroxide to create two different oxygen-radical species, with water (H+ + OH−) as a byproduct. The free radicals generated by this process then engage in secondary reactions. For example, the hydroxyl is a powerful, non- ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Fehling's Solution
In organic chemistry, Fehling's solution is a chemical reagent used to differentiate between water-soluble carbohydrate and ketone () functional groups, and as a test for reducing sugars and non-reducing sugars, supplementary to the Tollens' reagent test. The test was developed by German chemist Hermann von Fehling in 1849. Laboratory preparation Fehling's solution is prepared by combining two separate solutions: Fehling's A, which is a deep blue aqueous solution of copper(II) sulfate, and Fehling's B, which is a colorless solution of aqueous potassium sodium tartrate (also known as Rochelle salt) made strongly alkali with sodium hydroxide. These two solutions, stable separately, are combined when needed for the test because the copper(II) complex formed by their combination is not stable: it slowly decomposes into copper hydroxide in the alkaline conditions. The active reagent is a tartrate complex of Cu2+, which serves as an oxidizing agent. The tartrate serves as a ligand. Howe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Deacon Process
The Deacon process, invented by Henry Deacon, is a process used during the manufacture of alkalis (the initial end product was sodium carbonate) by the Leblanc process. Hydrogen chloride gas was converted to chlorine gas, which was then used to manufacture a commercially valuable bleaching powder, and at the same time the emission of waste hydrochloric acid was curtailed. To some extent this technically sophisticated process superseded the earlier manganese dioxide process. Process The process was based on the oxidation of hydrogen chloride: :4 HCl + O2 → 2 Cl2 + 2H2O The reaction takes place at about 400 to 450 °C in the presence of a variety of catalysts, including copper chloride (CuCl2). Three companies developed commercial processes for producing chlorine based on the Deacon reaction:Peter Schmittinger et al. "Chlorine," Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH Verlag GmbH & Co, 2006, *The Kel-Chlor process developed by the M. W. K ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chromyl Chloride
Chromyl chloride is the inorganic compound with the formula CrO2Cl2. It is a reddish brown compound that is a volatile liquid at room temperature, which is unusual for transition metal complexes. Preparation Chromyl chloride can be prepared by the reaction of potassium chromate or potassium dichromate with hydrogen chloride in the presence of sulfuric acid, followed by distillation. :K2Cr2O7 + 6 HCl → 2 CrO2Cl2 + 2 KCl + 3 H2O The sulfuric acid serves as the dehydration agent. It can also be prepared directly by exposing chromium trioxide to anhydrous hydrogen chloride gas. :CrO3 + 2 HCl ⇌ CrO2Cl2 + H2O The method used to prepare chromyl chloride is the basis for a qualitative test for chloride: a sample suspected of containing chloride is heated with a mixture of potassium dichromate and concentrated sulfuric acid. If chloride is present, chromyl chloride forms as evidenced by red fumes of CrO2Cl2. Analogous compounds are not formed with fluorides, bromides, iodides and cy ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Creutz–Taube Complex
The Creutz–Taube ion is the metal complex with the formula 5+. This cationic species has been heavily studied in an effort to understand the intimate details of inner sphere electron transfer, that is, how electrons move from one metal complex to another. The ion is named after Carol Creutz, who first prepared the complex, and her thesis advisor Henry Taube, who received a Nobel Prize in Chemistry for this and related discoveries on electron transfer. Properties The complex consists of two pentammineruthenium units linked to the nitrogen atoms in a bridging pyrazine ligand, which completes the octahedral coordination sphere of each metal. The important feature of the compound is that the two metals have apparent fractional oxidation states of +2.5. Normally metal ions, like most ions, have integer oxidation states. For example, ruthenium ammine complexes are typically +2 or +3. The fact that the oxidation states are half-integer indicates that the two Ru(NH3)5 centers are equi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclooctadiene
A cyclooctadiene (sometimes abbreviated COD) is any of several cyclic diene with the formula (CH2)4(C2H2)2. Focusing only on cis derivatives, four isomers are possible: 1,2-, which is an allene, 1,3-, 1,4-, and 1,5-. Commonly encountered isomers are the conjugated isomer 1,3-cyclooctadiene and 1,5-cyclooctadiene, which is used as a ligand for transition metal In chemistry, a transition metal (or transition element) is a chemical element in the d-block of the periodic table (groups 3 to 12), though the elements of group 12 (and less often group 3) are sometimes excluded. They are the elements that can ...s. These dienes are colorless volatile liquids.Thomas Schiffer, Georg Oenbrink “Cyclododecatriene, Cyclooctadiene, and 4-Vinylcyclohexene” in Ullmann’s Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. References External links1,5-Cyclooctadiene Cycloalkenes Dienes Eight-membered rings {{hydrocarbon-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Crabtree's Catalyst
Crabtree's catalyst is an organoiridium compound with the formula [1,5-Cyclooctadiene, C8H12IrTricyclohexylphosphine, P(C6H11)3pyridine, C5H5N]PF6. It is a homogeneous catalyst for hydrogenation and hydrogen-transfer reactions, developed by Robert H. Crabtree. This air stable orange solid is commercially available and known for its directed hydrogenation to give trans stereoselectivity with respective of directing group. Structure and synthesis The complex has a square planar molecular geometry, as expected for a d8 complex. It is prepared from cyclooctadiene iridium chloride dimer. Reactivity Crabtree’s catalyst is effective for the hydrogenations of mono-, di-, tri-, and tetra-substituted substrates. Whereas Wilkinson’s catalyst and the Schrock–Osborn catalyst do not catalyze the hydrogenation of a tetrasubstituted olefin, Crabtree’s catalyst does so to at high turnover frequencies (table). : The catalyst is reactive at room temperature. The reaction is robust without ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cornforth Reagent
The pyridinium dichromate (PDC) or Cornforth reagent is a pyridinium salt of dichromate with the chemical formula 5H5NHsub>2 r2O7 This compound is named after the Australian-British chemist Sir John Warcup Cornforth (b. 1917) who introduced it in 1962. The Cornforth reagent is a strong oxidizing agent which can convert primary and secondary alcohols to aldehydes and ketones respectively. In its chemical structure and functions it is closely related to other compounds made from hexavalent chromium oxide, such as pyridinium chlorochromate and Collins reagent. Because of their toxicity, these reagents are rarely used nowadays. Synthesis and properties The Cornforth reagent is prepared by slow addition of a concentrated aqueous solution of chromium trioxide to pyridine. The reaction may cause explosion, which is avoided by thoroughly dissolving the trioxide in water and cooling the solution by ice. The product is filtered, washed with acetone and dried, yielding an orange powder. Th ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
