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Osmocene
Osmocene is an organoosmium compound found as a white solid. It is a metallocene with the formula Os(C5H5)2. Synthesis Osmocene is commercially available. It may be prepared by the reaction of osmium tetroxide with hydrobromic acid followed by zinc and cyclopentadiene. It was first synthesized by Ernst Otto Fischer and Heinrich Grumbert via the reaction of osmium(IV) chloride with excess sodium cyclopentadienide in dimethoxyethane, where osmium(II) chloride is presumed to be an intermediate formed ''in situ''. Alternatively, cyclopentadienyl magnesium bromide could be reacted with osmium(IV) chloride, though this has worse yields. Properties Osmocene is a white solid. The molecular structure features an osmium ion sandwiched between two cyclopentadienyl rings. It is isomorphous to the lighter homologue ruthenocene, both crystallizing in an eclipsed conformation. This is in contrast to ferrocene, which crystallizes with its rings staggered. Compared to ferrocene an ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Metallocenes
A metallocene is a compound typically consisting of two cyclopentadienyl anions (, abbreviated Cp) bound to a metal center (M) in the oxidation state II, with the resulting general formula Closely related to the metallocenes are the metallocene derivatives, e.g. titanocene dichloride, vanadocene dichloride. Certain metallocenes and their derivatives exhibit catalytic properties, although metallocenes are rarely used industrially. Cationic group 4 metallocene derivatives related to p2ZrCH3sup>+ catalyze olefin polymerization. Some metallocenes consist of metal plus two cyclooctatetraenide anions (, abbreviated cot2−), namely the lanthanocenes and the actinocenes ( uranocene and others). Metallocenes are a subset of a broader class of compounds called sandwich compounds. In the structure shown at right, the two pentagons are the cyclopentadienyl anions with circles inside them indicating they are aromatically stabilized. Here they are shown in a staggered conformation. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ernst Otto Fischer
Ernst Otto Fischer (; 10 November 1918 – 23 July 2007) was a German chemist who won the Nobel Prize for pioneering work in the area of organometallic chemistry. Early life He was born in Solln, a borough of Munich. His parents were Karl T. Fischer, Professor of Physics at the Technical University of Munich (TU), and Valentine née Danzer. He graduated in 1937 with ''Abitur''. Before the completion of two years' compulsory military service, the Second World War broke out, and he served in Poland, France, and Russia. During a period of study leave, towards the end of 1941 he began to study chemistry at the Technical University of Munich. Following the end of the War, he was released by the Americans in the autumn of 1945 and resumed his studies. Training Fischer graduated from TUM in 1949. He then started his doctoral thesis as an assistant to Professor Walter Hieber in the Inorganic Chemistry Institute, His thesis was entitled "The Mechanisms of Carbon Monoxide Reactions of ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dimethoxyethane
Dimethoxyethane, also known as glyme, monoglyme, dimethyl glycol, ethylene glycol dimethyl ether, dimethyl cellosolve, and DME, is a colorless, aprotic, and liquid ether that is used as a solvent, especially in batteries. Dimethoxyethane is miscible with water. Production Monoglyme is produced industrially by the reaction of dimethylether with ethylene oxide: :CH3OCH3 + CH2CH2O → CH3OCH2CH2OCH3 Applications as solvent and ligand left, 144px, Structure of the coordination complex NbCl3(dimethoxyethane)(3-hexyne).{{cite journal , doi=10.1021/ja8100837, title=New Tantalum Ligand-Free Catalyst System for Highly Selective Trimerization of Ethylene Affording 1-Hexene: New Evidence of a Metallacycle Mechanism, year=2009, last1=Arteaga-Müller, first1=Rocío, last2=Tsurugi, first2=Hayato, last3=Saito, first3=Teruhiko, last4=Yanagawa, first4=Masao, last5=Oda, first5=Seiji, last6=Mashima, first6=Kazushi, journal=Journal of the American Chemical Society, volume=131, issue=15, pages=537 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Photocatalytic Water Splitting
Photocatalytic water splitting is an artificial photosynthesis process using photocatalysis for the dissociation of water (H2O) into hydrogen () and oxygen (). Only light energy ( photons), water, and a catalyst(s) are needed, since this is what naturally occurs in natural photosynthetic oxygen production and CO2 fixation. Hydrogen fuel production using water and light (photocatalytic water splitting), instead of petroleum, is an important renewable energy strategy. Concepts 2 mol is split into 1 mol and 2 mol using light in the process shown below. : \begin\\ \ce\\ \end The process of water-splitting is a highly endothermic process (Δ''H'' > 0). Water splitting occurs naturally in photosynthesis when the energy of four photons is absorbed and converted into chemical energy through a complex biochemical pathway (Dolai's or Kok's S-state diagrams). O–H bond homolysis in water requires energy of 6.5 - 6.9 eV (UV photon). Infrared light has sufficient energy to medi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Lewis Acid
A Lewis acid (named for the American physical chemist Gilbert N. Lewis) is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct. A Lewis base, then, is any species that has a filled orbital containing an electron pair which is not involved in bonding but may form a dative bond with a Lewis acid to form a Lewis adduct. For example, NH3 is a Lewis base, because it can donate its lone pair of electrons. Trimethylborane (Me3B) is a Lewis acid as it is capable of accepting a lone pair. In a Lewis adduct, the Lewis acid and base share an electron pair furnished by the Lewis base, forming a dative bond. In the context of a specific chemical reaction between NH3 and Me3B, a lone pair from NH3 will form a dative bond with the empty orbital of Me3B to form an adduct NH3•BMe3. The terminology refers to the contributions of Gilbert N. Lewis. From p. 142: "We are inclined to think of substances as p ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Adduct
An adduct (from the Latin ''adductus'', "drawn toward" alternatively, a contraction of "addition product") is a product of a direct addition of two or more distinct molecules, resulting in a single reaction product containing all atoms of all components. The resultant is considered a distinct molecular species. Examples include the addition of sodium bisulfite to an aldehyde to give a sulfonate. It can just be considered as a single product resulting from the direct combination of different molecules which comprises all the reactant molecules' atoms. Adducts often form between Lewis acids and Lewis bases. A good example is the formation of adducts between the Lewis acid borane and the oxygen atom in the Lewis bases, tetrahydrofuran (THF): BH3·O(CH2)4 or diethyl ether: BH3·O(CH3CH2)2. Many Lewis acids and Lewis bases reacting in the gas phase or in non-aqueous solvents to form adducts have been examined in the ECW model. Trimethylboron, trimethyltin chloride and bis(hex ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopentadienyl
Cyclopentadienyl can refer to * Cyclopentadienyl anion, or cyclopentadienide, **Cyclopentadienyl ligand A cyclopentadienyl complex is a coordination complex of a metal and cyclopentadienyl anion, cyclopentadienyl groups (, abbreviated as Cp−). Cyclopentadienyl ligands almost invariably bind to metals as a hapticity, pentahapto (''η''5-) bonding ... * Cyclopentadienyl radical, • * Cyclopentadienyl cation, See also * Pentadienyl {{Chemistry index ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chem
Chem may refer to: * Chemistry practical waali mam * Chemistry *Chemical * ''Chem'' (journal), a scientific journal published by Cell Press *Post apocalyptic slang for "drugs", medicinal or otherwise in the Fallout video game series. In Ancient Egyptian usage: * ''Khem'' (also spelt ''Chem''), the Egyptian word for "black" *Min (god), in the past erroneously named ''Khem'' CHEM may refer to : *A metabolic panel: for instance, CHEM-7, which is the basic metabolic panel * CHEM-DT, a Canadian television channel See also *Chemo (other) Chemo is a prefix meaning ''chemical'' and commonly used as an abbreviation for chemotherapy. Chemo may also refer to: People * Chemo (musician), an English musician now known as Forest DLG * Chemo Soto, a Puerto Rican politician * José del Sol ... * Kemi, a place in Finland {{disambig ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopentadienyl Magnesium Bromide
Cyclopentadienyl magnesium bromide is a chemical compound with the molecular formula . The molecule consists of a magnesium atom bonded to a bromine atom and a cyclopentadienyl group, a ring of five carbons each with one hydrogen atom. The compound is a Grignard reagent, a type of organometallic compound that features a magnesium atom bonded to a halogen atom and to a carbon atom of some organic functional group. This compound is of historic importance as the starting material for the first published synthesis of ferrocene by Peter Pauson and Thomas J. Kealy in 1951. Preparation The compound can be prepared by reacting cyclopentadiene with magnesium and bromoethane in anhydrous benzene Benzene is an organic chemical compound with the molecular formula C6H6. The benzene molecule is composed of six carbon atoms joined in a planar ring with one hydrogen atom attached to each. Because it contains only carbon and hydrogen ato .... References P. L. Pauson and T. J. Kealy ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
