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Beryllocene Conformation
Beryllocene is an organoberyllium compound with the chemical formula Be(C5H5)2, first prepared in 1959. The colorless substance can be crystallized from petroleum ether in the form of white needles at −60 °C and decomposes quickly upon contact with atmospheric oxygen and water. Preparation Beryllocene can be prepared by reacting beryllium chloride and sodium cyclopentadienide in benzene or diethyl ether: :\mathrm Properties Physical In contrast to the uncharged metallocenes of the transition metals V, Cr, Fe, Co, Ni, Ru and Os, which have a strictly symmetrical and therefore dipoleless structure, beryllocene has an electric dipole moment of 2.46 Debye (in benzene), or 2.24 Debye (in cyclohexane), indicating asymmetry of the molecule. In the IR spectrum there are signals at 1524, 1610, 1669, 1715 and 1733 cm−1, which also indicate that the structure does correspond to that of ferrocene. In contrast, the nuclear magnetic resonance spectrum shows only ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Organoberyllium Compound
Organoberyllium chemistry involves the synthesis and properties of organometallic compounds featuring the group 2 alkaline earth metal beryllium (Be). The area remains less developed relative to the chemistry of other main-group elements, because Be compounds are toxic and few applications have been found. Structure Homoleptic compounds The coordination number of Be in organoberyllium compounds ranges from two to four. Dimethylberyllium and dimethylmagnesium adopts the same structure. Diethylberyllium, however, does not structurally resemble diethylmagnesium (which has the same structure as dimethylmagnesium). This contrast is attributed to the small size of Be relative to its heavier congener Mg: Be is one of the smallest atoms on the periodic table. Dineopentylberyllium and many other dialkyl derivatives has been reported. The phenyl derivative is represented by trimeric Be3Ph6. A terphenyl derivative is known. With bulky aryl ligands three-coordination is observed, see . ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
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. The dipole itself is a vector whose direction coincides with the position vector of the positive charge with respect to the negative charge: : p = ''q''r. named in honour of the physicist Peter J. W. Debye. It is defined as statcoulomb-centimetres.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 ol ... [...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 metallic element, 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 or vanadocene dichloride. Certain metallocenes and their derivatives exhibit catalysis, catalytic properties, although metallocenes are rarely used industrially. Cationic group 4 metallocene derivatives related to [Cp2ZrCH3]+ catalyze Ziegler–Natta catalyst, 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 aromaticity, aromatically ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Carcinogen
A carcinogen () is any agent that promotes the development of cancer. Carcinogens can include synthetic chemicals, naturally occurring substances, physical agents such as ionizing and non-ionizing radiation, and biologic agents such as viruses and bacteria. Most carcinogens act by creating mutations in DNA that disrupt a cell's normal processes for regulating growth, leading to uncontrolled cellular proliferation. This occurs when the cell's DNA repair processes fail to identify DNA damage allowing the defect to be passed down to daughter cells. The damage accumulates over time. This is typically a multi-step process during which the regulatory mechanisms within the cell are gradually dismantled allowing for unchecked cellular division. The specific mechanisms for carcinogenic activity is unique to each agent and cell type. Carcinogens can be broadly categorized, however, as activation-dependent and activation-independent which relate to the agent's ability to engage dir ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Beryllium
Beryllium is a chemical element; it has Symbol (chemistry), symbol Be and atomic number 4. It is a steel-gray, hard, strong, lightweight and brittle alkaline earth metal. It is a divalent element that occurs naturally only in combination with other elements to form minerals. Gemstones high in beryllium include beryl (Aquamarine (gemstone), aquamarine, emerald, red beryl) and chrysoberyl. It is a Abundance of the chemical elements#Universe, relatively rare element in the universe, usually occurring as a product of the spallation of larger atomic nuclei that have collided with cosmic rays. Within the cores of stars, beryllium is depleted as it is fused into heavier elements. Beryllium constitutes about 0.0004 percent by mass of Earth's crust. The world's annual beryllium production of 220 tons is usually manufactured by extraction from the mineral beryl, a difficult process because beryllium bonds strongly to oxygen. In structural applications, the combination of high flexural ri ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Iron(II) Chloride
Iron(II) chloride, also known as ferrous chloride, is the chemical compound of formula FeCl2. It is a paramagnetic solid with a high melting point. The compound is white, but typical samples are often off-white. FeCl2 crystallizes from water as the greenish tetrahydrate, which is the form that is most commonly encountered in commerce and the laboratory. There is also a dihydrate. The compound is highly soluble in water, giving pale green solutions. Production Hydrated forms of ferrous chloride are generated by treatment of wastes from steel production with hydrochloric acid. Such solutions are designated "spent acid," or "pickle liquor" especially when the hydrochloric acid is not completely consumed: :Fe + 2 HCl → FeCl2 + H2 The production of ferric chloride involves the use of ferrous chloride. Ferrous chloride is also a byproduct from the production of titanium, since some titanium ores contain iron.Egon Wildermuth, Hans Stark, Gabriele Friedrich, Franz Ludw ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ferrocene
Ferrocene is an organometallic chemistry, organometallic compound with the formula . The molecule is a Cyclopentadienyl complex, complex consisting of two Cyclopentadienyl anion, cyclopentadienyl rings sandwiching a central iron atom. It is an orange solid with a camphor-like odor that Sublimation (phase transition), sublimes above room temperature, and is soluble in most organic solvents. It is remarkable for its stability: it is unaffected by air, water, strong bases, and can be heated to 400 °C without decomposition. In oxidizing conditions it can reversibly react with strong acids to form the ferrocenium cation . Ferrocene and the ferrocenium cation are sometimes abbreviated as Fc and respectively. The first reported synthesis of ferrocene was in 1951. Its unusual stability puzzled chemists, and required the development of new theory to explain its formation and bonding. The discovery of ferrocene and its many Structural analog, analogues, known as metallocenes, sparke ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Magnesocene
Magnesocene, also known as bis(cyclopentadienyl)magnesium(II) and sometimes abbreviated as MgCp2, is an organometallic compound with the formula Mg(η5-C5H5)2. It is white powder or crystals. It is an example of an s-block Main-group element, main group sandwich compound, structurally related to the d-block element metallocenes, and consists of a central magnesium atom sandwiched between two Cyclopentadienyl complex, cyclopentadienyl rings. Properties Magnesocene is a white solid at room temperature. It has a melting point of 176 °C, though at atmospheric pressures it Sublimation (phase transition), sublimes at 100 °C. Unlike ferrocene, magnesocene displays slight dissociation and subsequent ion association in polar, electron-donating solvents (such as ether and THF). : : : While ferrocene is stable at ambient conditions, magnesocene decomposes rapidly on exposure to oxygen or moisture, and as such must be synthesized and stored under inert conditions. Structure ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopentadiene
Cyclopentadiene is an organic compound with the chemical formula, formula C5H6. It is often abbreviated CpH because the cyclopentadienyl anion is abbreviated Cp−. This colorless liquid has a strong and unpleasant odor. At room temperature, this cyclic diene dimer (chemistry), dimerizes over the course of hours to give dicyclopentadiene via a Diels–Alder reaction. This dimer can be retro-Diels–Alder reaction, restored by heating to give the monomer. The compound is mainly used for the production of cyclopentene and its derivatives. It is popularly used as a precursor to the cyclopentadienyl anion (Cp−), an important ligand in cyclopentadienyl complexes in organometallic chemistry. Production and reactions Cyclopentadiene production is usually not distinguished from dicyclopentadiene since they interconvert. They are obtained from coal tar (about 10–20 g/tonne, t) and by steam Cracking (chemistry), cracking of Petroleum naphtha, naphtha (about 14 kg/t) ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Beryllium Hydroxide
Beryllium hydroxide, Be(OH)2, is an amphoteric hydroxide, dissolving in both acids and alkalis. Industrially, it is produced as a by-product in the extraction of beryllium metal from the ores beryl and bertrandite. The natural pure beryllium hydroxide is rare (in form of the mineral behoite, orthorhombic) or very rare (clinobehoite, monoclinic).Mindat, http://www.mindat.org/min-1066.html When alkali is added to beryllium salt solutions the α-form (a gel) is formed. If this left to stand or boiled, the rhombic β-form precipitates.Mary Eagleson, 1994, Concise encyclopedia chemistry, Walter de Gruyter, This has the same structure as zinc hydroxide, Zn(OH)2, with tetrahedral beryllium centers. Reactions Beryllium hydroxide is difficult to dissolve in water. With alkalis it dissolves to form the tetrahydroxoberyllate (also known as tetrahydroxidoberyllate) anion, e(OH)4sup>2−.Egon Wiberg, Arnold Frederick Holleman (2001) ''Inorganic Chemistry'', Elsevier With sodium hydroxide so ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tetrahydrofuran
Tetrahydrofuran (THF), or oxolane, is an organic compound with the formula (CH2)4O. The compound is classified as heterocyclic compound, specifically a cyclic ether. It is a colorless, water- miscible organic liquid with low viscosity. It is mainly used as a precursor to polymers. Being polar and having a wide liquid range, THF is a versatile solvent. It is an isomer of another solvent, butanone. Production About 200,000 tonnes of tetrahydrofuran are produced annually. The most widely used industrial process involves the acid-catalyzed dehydration of 1,4-Butanediol, 1,4-butanediol. Ashland Inc., Ashland/ISP is one of the biggest producers of this chemical route. The method is similar to the production of diethyl ether from ethanol. The butanediol is derived from Condensation reaction, condensation of acetylene with formaldehyde followed by hydrogenation. DuPont developed a process for producing THF by oxidizing Butane#Isomers, ''n''-butane to crude maleic anhydride, follow ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Arne Haaland
Arne Haaland (15 February 1936 – 13 October 2023) was a Norwegian chemist. He took the dr. philos. degree at the University of Oslo in 1969 and was an associate professor in chemistry at the University of Oslo from 1964 to 1984, and then professor until his retirement. He was a fellow of the Norwegian Academy of Science and Letters. Haaland ran a laboratory for gas electron diffraction. He, his co-workers and colleagues determined the structures of umpteen important chemical compounds in the gas phase. His main field of research was the organometallic Organometallic chemistry is the study of organometallic compounds, chemical compounds containing at least one chemical bond between a carbon atom of an organic molecule and a metal, including alkali, alkaline earth, and transition metals, and so ... compounds. The list of such structure determinations includes the controversially debated beryllocene, dibenzene chromium, ferrocene, the structure of the phosphorus oxides P4O1 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
