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Molybdenum Dichloride Dioxide
Molybdenum dichloride dioxide is the inorganic compound with the formula . It is a yellow diamagnetic solid that is used as a precursor to other molybdenum compounds. Molybdenum dichloride dioxide is one of several oxychlorides of molybdenum. Structure Gaseous molybdenum dichloride dioxide is a monomer, but upon condensation, it polymerizes to give a coordination polymer of uncertain structure. Preparation The compound is most easily prepared by treatment molybdenum trioxide with concentrated hydrochloric acid: :MoO3 + 2 HCl → MoO2Cl2 + H2O MoO2Cl2 can also be prepared from MoOCl4: :MoOCl4 + O(Si(CH3)3)2 → MoO2Cl2 + 2 ClSi(CH3)3 It is also prepared by chlorination of molybdenum dioxide: :MoO2 + Cl2 → MoO2Cl2 It is also prepared by chlorination of molybdenum trixoide: :MoO3 + Cl2 → MoO2Cl2 Reactions Many bisadducts are known of the type . These octahedral molecular complexes are soluble in organic solvents. With bulky anilines, it converts to the diimido complex . This ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Molybdenum Difluoride Dioxide
Molybdenum difluoride dioxide is the inorganic compound with the formula . It is a white, diamagnetic, volatile solid. Structure : Gaseous molybdenum difluoride dioxide is a tetrahedral molecule. According to X-ray crystallography, the solid is a coordination polymer consisting of trigonal primatic chains of made by linking monomers. The fluoride and oxide positions are disordered. A similar motif is adopted by titanium tetrafluoride. Synthesis and reactions The compound can be obtained by thermal decomposition of the sodium tetrafluorodioxomolybdate(VI) , which in turn is obtained from sodium molybdate: : Heating sodium tetrafluorodioxomolybdate(VI) to 400 °C gives monomeric molybdenum difluoride dioxide, which polymerizes upon condensation: : The compound also arises by hydrolysis of molybdenum oxytetrafluoride: : The compound dissolves in dimethylformamide to give a adduct In chemistry, an adduct (; alternatively, a contraction of "addition product") is a product ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Adduct
In chemistry, an adduct (; 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 be considered as a single product resulting from the direct combination of different molecules which comprises all atoms of the reactant molecules. 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): or diethyl ether: . 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. Trimethylborane, trimethyltin chloride and bis(hexafluoroacetylacetonato)copper(II) are examples of Lewi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Sublimation (phase Transition)
Sublimation is the Phase transition, transition of a substance directly from the solid to the gas state, without passing through the liquid state. The verb form of sublimation is ''sublime'', or less preferably, ''sublimate''. ''Sublimate'' also refers to the product obtained by sublimation. The point at which sublimation occurs rapidly (for further details, see #False correspondence with vaporization, below) is called critical sublimation point, or simply sublimation point. Notable examples include sublimation of dry ice at room temperature and atmospheric pressure, and that of solid iodine with heating. The reverse process of sublimation is deposition (phase transition), ''deposition'' (also called ''desublimation''), in which a substance passes directly from a gas to a solid phase, without passing through the liquid state. Technically, all solids may sublime, though most sublime at extremely low rates that are hardly detectable under usual conditions. At standard condi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Butyl Group
In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula , derived from either of the two isomers (''n''-butane and isobutane) of butane. The isomer ''n''-butane can connect in two ways, giving rise to two "-butyl" groups: * If it connects at one of the two terminal carbon atoms, it is normal butyl or ''n''-butyl: (preferred IUPAC name: butyl) * If it connects at one of the non-terminal (internal) carbon atoms, it is secondary butyl or ''sec''-butyl: (preferred IUPAC name: butan-2-yl) The second isomer of butane, isobutane, can also connect in two ways, giving rise to two additional groups: * If it connects at one of the three terminal carbons, it is isobutyl: (preferred IUPAC name: 2-methylpropyl) * If it connects at the central carbon, it is tertiary butyl, ''tert''-butyl or ''t''-butyl: (preferred IUPAC name: ''tert''-butyl) Nomenclature According to IUPAC nomenclature, "isobutyl", "''sec''-butyl", and "''tert''- ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Schrock Carbene
A transition metal carbene complex is an organometallic compound featuring a divalent carbon ligand, itself also called a carbene. Carbene complexes have been synthesized from most transition metals and f-block metals, using many different synthetic routes such as nucleophilic addition and alpha-hydrogen abstraction. The term carbene ligand is a formalism since many are not directly derived from carbenes and most are much less reactive than lone carbenes. Described often as , carbene ligands are intermediate between alkyls and carbynes . Many different carbene-based reagents such as Tebbe's reagent are used in synthesis. They also feature in catalytic reactions, especially alkene metathesis, and are of value in both industrial heterogeneous and in homogeneous catalysis for laboratory- and industrial-scale preparation of fine chemicals. Classification Metal carbene complexes are often classified into two types. The Fischer carbenes, named after Ernst Otto Fischer, feature stro ... [...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). Together with a high-permittivity solvent (e.g. propylene carbonate), dimethoxyethane is used as the low-viscosity component of the solvent for electrolytes of lithium batteries. In the laboratory, DME is used as a coordinating solvent. Dimethoxyethane is often used as a higher-boiling-point alternative to diethyl ether and tetrahydrofuran. Dimethoxyethane acts as a bidentate ligand for some metal cations. It is therefore often used in organometallic chemist ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aryl Group
In organic chemistry, an aryl is any functional group or substituent derived from an aromatic ring, usually an aromatic hydrocarbon, such as phenyl and naphthyl. "Aryl" is used for the sake of abbreviation or generalization, and "Ar" is used as a placeholder for the aryl group in chemical structure diagrams, analogous to “R” used for any organic substituent. “Ar” is not to be confused with the elemental symbol for argon. A simple aryl group is phenyl (), a group derived from benzene. Examples of other aryl groups consist of: * The tolyl group () which is derived from toluene (methylbenzene) * The xylyl group (), which is derived from xylene (dimethylbenzene) * The naphthyl group (), which is derived from naphthalene Arylation is the process in which an aryl group is attached to a substituent. It is typically achieved by cross-coupling reactions. Nomenclature The simplest aryl group is phenyl, which is made up of a benzene ring with one of its hydrogen atom repla ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aniline
Aniline (From , meaning ' indigo shrub', and ''-ine'' indicating a derived substance) is an organic compound with the formula . Consisting of a phenyl group () attached to an amino group (), aniline is the simplest aromatic amine. It is an industrially significant commodity chemical, as well as a versatile starting material for fine chemical synthesis. Its main use is in the manufacture of precursors to polyurethane, dyes, and other industrial chemicals. Like most volatile amines, it has the odor of rotten fish. It ignites readily, burning with a smoky flame characteristic of aromatic compounds. It is toxic to humans. Relative to benzene, aniline is "electron-rich". It thus participates more rapidly in electrophilic aromatic substitution reactions. Likewise, it is also prone to oxidation: while freshly purified aniline is an almost colorless oil, exposure to air results in gradual darkening to yellow or red, due to the formation of strongly colored, oxidized impurities. Ani ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ether
In organic chemistry, ethers are a class of compounds that contain an ether group, a single oxygen atom bonded to two separate carbon atoms, each part of an organyl group (e.g., alkyl or aryl). They have the general formula , where R and R′ represent the organyl groups. Ethers can again be classified into two varieties: if the organyl groups are the same on both sides of the oxygen atom, then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. A typical example of the first group is the solvent and anaesthetic diethyl ether, commonly referred to simply as "ether" (). Ethers are common in organic chemistry and even more prevalent in biochemistry, as they are common linkages in carbohydrates and lignin. Structure and bonding Ethers feature bent linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of ox ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Molybdenum Dioxide
Molybdenum dioxide is the chemical compound with the formula MoO. It is a violet-colored solid and is a metallic conductor. The mineralogical form of this compound is called tugarinovite, and is only very rarely found. Structure It crystallizes in a monoclinic cell, and has a distorted rutile, ( TiO2) crystal structure. In TiO the oxide anions are close packed and titanium atoms occupy half of the octahedral interstices (holes). In MoO the octahedra are distorted, the Mo atoms are off-centre, leading to alternating short and long Mo – Mo distances and Mo-Mo bonding. The short Mo – Mo distance is 251 pm which is less than the Mo – Mo distance in the metal, 272.5 pm. The bond length is shorter than would be expected for a single bond. The bonding is complex and involves a delocalisation of some of the Mo electrons in a conductance band accounting for the metallic conductivity. Preparation MoO can be prepared : *by reduction of MoO3 with Mo over the course of 70 hours at ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Molybdenum Oxytetrachloride
Molybdenum oxytetrachloride is the inorganic compound with the formula . This thermally unstable, dark green solid is used to prepare other complexes of molybdenum. Its molecule adopts a square pyramidal molecular geometry of C4v symmetry. As for other Mo(VI) compounds, it is diamagnetic. It decomposes thermally to . Preparation It is prepared by treating molybdenum pentachloride with oxygen. It also arises by chlorination of molybdenum trioxide: : See also * Molybdenum dichloride dioxide Molybdenum dichloride dioxide is the inorganic compound with the formula . It is a yellow diamagnetic solid that is used as a precursor to other molybdenum compounds. Molybdenum dichloride dioxide is one of several oxychlorides of molybdenum. Stru ... References {{Molybdenum compounds Oxychlorides Molybdenum(VI) compounds ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Polyhedron (journal)
''Polyhedron'' is a peer-reviewed scientific journal covering the field of inorganic chemistry. It was established in 1955 as the ''Journal of Inorganic and Nuclear Chemistry'' and is published by Elsevier. Abstracting and indexing ''Polyhedron'' is abstracted and indexed in: According to the ''Journal Citation Reports'', the journal has a 2020 impact factor The impact factor (IF) or journal impact factor (JIF) of an academic journal is a type of journal ranking. Journals with higher impact factor values are considered more prestigious or important within their field. The Impact Factor of a journa ... of 3.052. References External links * {{Official Website, http://www.journals.elsevier.com/polyhedron/ Inorganic chemistry journals Elsevier academic journals Academic journals established in 1955 English-language journals ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
