Sodium Phosphide
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Sodium Phosphide
Sodium phosphide is the inorganic compound with the formula Na3P. It is a black solid. It is often described as Na+ salt of the P3− anion. Na3P is a source of the highly reactive phosphide anion. It should not be confused with sodium phosphate, Na3PO4. In addition to Na3P, five other binary compositions of sodium and phosphorus are known: NaP, Na3P7, Na3P11, NaP7, and NaP15. Structure and Properties The compound crystallizes in a hexagonal motif, often called the sodium arsenide structure. Like K3P, solid Na3P features pentacoordinate P centers. Preparation The first preparation of Na3P was first reported in the mid-19th century. French researcher, Alexandre Baudrimont prepared sodium phosphide by treating molten sodium with phosphorus pentachloride. : 8 Na(l) + PCl5 → 5 NaCl + Na3P Many different routes to Na3P have been described. Due to its flammability and toxicity, Na3P (and related salts) is often prepared and used in situ. White phosphorus is reduced by sodi ...
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Hydrolysis
Hydrolysis (; ) is any chemical reaction in which a molecule of water breaks one or more chemical bonds. The term is used broadly for substitution reaction, substitution, elimination reaction, elimination, and solvation reactions in which water is the nucleophile. Biological hydrolysis is the cleavage of biomolecules where a water molecule is consumed to effect the separation of a larger molecule into component parts. When a carbohydrate is broken into its component sugar molecules by hydrolysis (e.g., sucrose being broken down into glucose and fructose), this is recognized as saccharification. Hydrolysis reactions can be the reverse of a condensation reaction in which two molecules join into a larger one and eject a water molecule. Thus hydrolysis adds water to break down, whereas condensation builds up by removing water. Types Usually hydrolysis is a chemical process in which a molecule of water is added to a substance. Sometimes this addition causes both the substance and w ...
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Annales De Chimie Et De Physique
__NOTOC__ ''Annales de chimie et de physique'' ( French for ''Annals of Chemistry and Physics'') is a scientific journal founded in Paris, France, in 1789 under the title ''Annales de chimie''. One of the early editors was the French chemist Antoine Lavoisier. Lavoisier, an aristocrat, was guillotined in May 1794, ostensibly for tax fraud: and the journal was not published from 1794 to 1796 while the Reign of Terror was at its height under the French Directory. In 1815, it became the ''Annales de chimie et de physique'', and was published under that name for the next 100 years. In 1914, it split into two successor journals. The first one, '' Annales de physique'', was latterly published by EDP Sciences under the same name up to 2009, when it became integrated in the ''European Physical Journal'' series as the '' European Physical Journal H – Historical Perspectives on Contemporary Physics''. The second successor, ''Annales de chimie'', later became '' Annales de chimie: Scien ...
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Propylene
Propylene, also known as propene, is an unsaturated organic compound with the chemical formula CH3CH=CH2. It has one double bond, and is the second simplest member of the alkene class of hydrocarbons. It is a colorless gas with a faint petroleum-like odor. Production Steam cracking The dominant technology for producing propylene is steam cracking. The same technology is applied to ethane to ethylene. These two conversions are the #2 and #1 processes in the chemical industry, as judged by their scale. In this process, propane undergoes dehydrogenation. The by-product is hydrogen: :CH3CH2CH3 → CH3CH=CH2 + H2 The yield of propene is about 85 m%. By-products are usually used as fuel for the propane dehydrogenation reaction. Steam cracking is one of the most energy-intensive industrial processes. The feedstock is naphtha or propane, especially in the Middle East, where there is an abundance of propane from oil/gas operations. Propene can be separated by fractional distilla ...
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Polymerization
In polymer chemistry, polymerization (American English), or polymerisation (British English), is a process of reacting monomer, monomer molecules together in a chemical reaction to form polymer chains or three-dimensional networks. There are many forms of polymerization and different systems exist to categorize them. In chemical compounds, polymerization can occur via a variety of reaction mechanisms that vary in complexity due to the functional groups present in the reactants and their inherent steric effects. In more straightforward polymerizations, alkenes form polymers through relatively simple free-radical reaction, radical reactions; in contrast, reactions involving substitution at a carbonyl group require more complex synthesis due to the way in which reactants polymerize. Alkanes can also be polymerized, but only with the help of strong acids. As alkenes can polymerize in somewhat straightforward radical reactions, they form useful compounds such as polyethylene and p ...
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Polymer
A polymer (; Greek '' poly-'', "many" + ''-mer'', "part") is a substance or material consisting of very large molecules called macromolecules, composed of many repeating subunits. Due to their broad spectrum of properties, both synthetic and natural polymers play essential and ubiquitous roles in everyday life. Polymers range from familiar synthetic plastics such as polystyrene to natural biopolymers such as DNA and proteins that are fundamental to biological structure and function. Polymers, both natural and synthetic, are created via polymerization of many small molecules, known as monomers. Their consequently large molecular mass, relative to small molecule compounds, produces unique physical properties including toughness, high elasticity, viscoelasticity, and a tendency to form amorphous and semicrystalline structures rather than crystals. The term "polymer" derives from the Greek word πολύς (''polus'', meaning "many, much") and μέρος (''meros'' ...
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Catalyst
Catalysis () is the process of increasing the rate of a chemical reaction by adding a substance known as a catalyst (). Catalysts are not consumed in the reaction and remain unchanged after it. If the reaction is rapid and the catalyst recycles quickly, very small amounts of catalyst often suffice; mixing, surface area, and temperature are important factors in reaction rate. Catalysts generally react with one or more reactants to form intermediates that subsequently give the final reaction product, in the process of regenerating the catalyst. Catalysis may be classified as either homogeneous, whose components are dispersed in the same phase (usually gaseous or liquid) as the reactant, or heterogeneous, whose components are not in the same phase. Enzymes and other biocatalysts are often considered as a third category. Catalysis is ubiquitous in chemical industry of all kinds. Estimates are that 90% of all commercially produced chemical products involve catalysts at some s ...
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Materials Letters
''Materials Letters'' is an interdisciplinary, peer-reviewed journal published by Elsevier which according to its website "is dedicated to publishing novel, cutting edge reports of broad interest to the materials community." Abstracting and indexing The journal is indexed in Inspec. 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 scientometric index calculated by Clarivate that reflects the yearly mean number of citations of articles published in the last two years in a given journal, as i ... of 3.423. References External links * Materials science journals Elsevier academic journals English-language journals Publications established in 1982 {{science-journal-stub ...
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Dimethylformamide
Dimethylformamide is an organic compound with the formula ( CH3)2NC(O)H. Commonly abbreviated as DMF (although this initialism is sometimes used for dimethylfuran, or dimethyl fumarate), this colourless liquid is miscible with water and the majority of organic liquids. DMF is a common solvent for chemical reactions. Dimethylformamide is odorless, but technical-grade or degraded samples often have a fishy smell due to impurity of dimethylamine. Dimethylamine degradation impurities can be removed by sparging samples with an inert gas such as argon or by sonicating the samples under reduced pressure. As its name indicates, it is structurally related to formamide, having two methyl groups in the place of the two hydrogens. DMF is a polar (hydrophilic) aprotic solvent with a high boiling point. It facilitates reactions that follow polar mechanisms, such as SN2 reactions. Structure and properties As for most amides, the spectroscopic evidence indicates partial double bond charact ...
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Indium(III) Chloride
Indium(III) chloride is the chemical compound with the formula In Cl3. This salt is a white, flaky solid with applications in organic synthesis as a Lewis acid. It is also the most available soluble derivative of indium. Synthesis and structure Being a relatively electropositive metal, indium reacts quickly with chlorine to give the trichloride. Indium trichloride is very soluble and deliquescent. A synthesis has been reported using an electrochemical cell in a mixed methanol-benzene solution. Like AlCl3 and TlCl3, InCl3 crystallizes as a layered structure consisting of a close-packed chloride arrangement containing layers of octahedrally coordinated In(III) centers,Egon Wiberg, Arnold Frederick Holleman (2001) ''Inorganic Chemistry'', Elsevier a structure akin to that seen in YCl3.Wells, A.F. Structural Inorganic Chemistry, Oxford: Clarendon Press, 1984. . In contrast, GaCl3 crystallizes as dimers containing Ga2Cl6. Molten InCl3 conducts electricity, whereas AlCl3 doe ...
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Indium Phosphide
Indium phosphide (InP) is a binary semiconductor composed of indium and phosphorus. It has a face-centered cubic ("zincblende") crystal structure, identical to that of GaAs and most of the III-V semiconductors. Manufacturing Indium phosphide can be prepared from the reaction of white phosphorus and indium iodide at 400 °C., also by direct combination of the purified elements at high temperature and pressure, or by thermal decomposition of a mixture of a trialkyl indium compound and phosphine. Uses InP is used in high-power and high-frequency electronics because of its superior electron velocity with respect to the more common semiconductors silicon and gallium arsenide. It was used with indium gallium arsenide to make a record breaking pseudomorphic heterojunction bipolar transistor that could operate at 604 GHz. It also has a direct bandgap, making it useful for optoelectronics devices like laser diodes. The company Infinera uses indium phosphide as its major techn ...
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Tris(trimethylsilyl)phosphine
Tris(trimethylsilyl)phosphine is the organophosphorus compound with the formula P(SiMe3)3 (Me = methyl). It is a colorless liquid that ignites in air and hydrolyses readily. Synthesis Tris(trimethylsilyl)phosphine is prepared by treating trimethylsilyl chloride, white phosphorus, and sodium-potassium alloy: :1/4 P4 + 3 Me3SiCl + 3 K → P(SiMe3)3 + 3 KCl Several other methods exist. Reactions The compound hydrolyzes to give phosphine: :P(SiMe3)3 + 3 H2O → PH3 + 3 HOSiMe3 Treatment of certain acyl chlorides with tris(trimethylsilyl)phosphine gives phosphaalkynes, one example being tert-butylphosphaacetylene. : Reaction with potassium tert-butoxide cleaves one P-Si bond, giving the phosphide salt:{{cite book, chapter=Phosphaalkynes , author1=Russell, Christopher A. , author2=Townsend, Nell S., editor1=Kamer, Paul C. J. , editor2=Van Leeuwen, Piet W. N. M , title=Phosphorus(III) Ligands in Homogeneous Catalysis, year=2012, pages=343–354, publisher=Wiley-VCH ...
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Sodium Naphthalenide
Sodium naphthalene is an organic salt with the chemical formula Na+. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na+. Preparation and properties The alkali metal naphthalene salts are prepared by stirring the metal with naphthalene in an ethereal solvent, usually as tetrahydrofuran or dimethoxyethane. The resulting salt is dark green. The anion is a radical, giving a strong EPR signal near ''g'' = 2.0. Its deep green color arises from absorptions centered at 463 and 735 nm. Several solvates of sodium naphthalenide have been characterized by X-ray crystallography. The effects are subtle, the outer pair of CH−CH bonds contract by 3  pm and the other nine C−C bonds elongate by 2–3 pm. The net effect is that reduction weakens the bonding. Reactions ;Redox Wi ...
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