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Phosphide
In chemistry, a phosphide is a compound containing the ion or its equivalent. Many different phosphides are known, with widely differing structures. Most commonly encountered on the binary phosphides, i.e. those materials consisting only of phosphorus and a less electronegative element. Numerous are polyphosphides, which are solids consisting of anionic chains or clusters of phosphorus. Phosphides are known with the majority of less electronegative elements with the exception of Hg, Pb, Sb, Bi, Te, and Po.Von Schnering, H.G. and Hönle , W. (1994) "Phosphides - Solid-state Chemistry" in ''Encyclopedia of Inorganic Chemistry''. R. Bruce King (ed.). John Wiley & Sons Finally, some phosphides are molecular. Binary phosphides Binary phosphides include phosphorus and one other element. An example of a group 1 phosphide is sodium phosphide (). Other notable examples include aluminium phosphide () and calcium phosphide (), which are used as pesticides, exploiting their tendenc ...
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Phosphides
In chemistry, a phosphide is a compound containing the ion or its equivalent. Many different phosphides are known, with widely differing structures. Most commonly encountered on the binary phosphides, i.e. those materials consisting only of phosphorus and a less electronegative element. Numerous are polyphosphides, which are solids consisting of anionic chains or clusters of phosphorus. Phosphides are known with the majority of less electronegative elements with the exception of Hg, Pb, Sb, Bi, Te, and Po.Von Schnering, H.G. and Hönle , W. (1994) "Phosphides - Solid-state Chemistry" in ''Encyclopedia of Inorganic Chemistry''. R. Bruce King (ed.). John Wiley & Sons Finally, some phosphides are molecular. Binary phosphides Binary phosphides include phosphorus and one other element. An example of a group 1 phosphide is sodium phosphide (). Other notable examples include aluminium phosphide () and calcium phosphide (), which are used as pesticides, exploiting their tendenc ...
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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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Aluminium Phosphide
Aluminium phosphide is a highly toxic inorganic compound with the chemical formula AlP, used as a wide band gap semiconductor and a fumigant. This colorless solid is generally sold as a grey-green-yellow powder due to the presence of impurities arising from hydrolysis and oxidation. Properties AlP crystals are dark grey to dark yellow in color and have a zincblende crystal structure with a lattice constant of 5.4510 Å at 300 K. They are thermodynamically stable up to . Aluminium phosphide reacts with water or acids to release phosphine: :AlP + 3 H2O → Al(OH)3 + PH3 :AlP + 3 H+ → Al3+ + PH3 Preparation AlP is synthesized by combination of the elements: : 4Al + P4 → 4AlP : Caution must be taken to avoid exposing the AlP to any sources of moisture, as this generates toxic phosphine gas. Phosphine also poses fire hazards, as it is a dangerous pyrophoric compound, igniting easily in air. Uses Pesticide AlP is used as a rodenticide, insecticide, and fumigant for st ...
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Phosphine
Phosphine (IUPAC name: phosphane) is a colorless, flammable, highly toxic compound with the chemical formula , classed as a pnictogen hydride. Pure phosphine is odorless, but technical grade samples have a highly unpleasant odor like rotting fish, due to the presence of substituted phosphine and diphosphane (). With traces of present, is spontaneously flammable in air ( pyrophoric), burning with a luminous flame. Phosphine is a highly toxic respiratory poison, and is immediately dangerous to life or health at 50 ppm. Phosphine has a trigonal pyramidal structure. Phosphines are compounds that include and the organophosphines, which are derived from by substituting one or more hydrogen atoms with organic groups. They have the general formula . Phosphanes are saturated phosphorus hydrides of the form , such as triphosphane. Phosphine, PH3, is the smallest of the phosphines and the smallest of the phosphanes. History Philippe Gengembre (1764–1838), a student of Lavois ...
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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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Copper Phosphide
Copper phosphide, , also copper(I) phosphide, cuprous phosphide, cuprophosphorus and phosphor copper, is a compound of copper and phosphorus, a phosphide of copper. It has the appearance of yellowish-grey very brittle mass of crystalline structure. It does not react with water. Recent crystallographic investigations have proven Cu3P to be copper deficient, which means that the sum formula of this compound is more accurately expressed as Cu3−xP. Copper phosphide has a role in copper alloys, namely in phosphor bronze. It is a very good deoxidizer of copper. Copper phosphide can be produced in a reverberatory furnace or in a crucible, e.g. by a reaction of red phosphorus with a copper-rich material. It can also be prepared photochemically, by irradiating cupric hypophosphite with ultraviolet radiation. It can also be produced by reducing copper(II) phosphate with aluminum metal When subjected to ultraviolet light, copper phosphide shows fluorescence. A blue-black film of copper ...
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Calcium Phosphide
Calcium phosphide (CP) is the inorganic compound with the formula Ca3P2. It is one of several phosphides of calcium, being described as the salt-like material composed of Ca2+ and P3−. Other, more exotic calcium phosphides have the formula CaP, CaP3, Ca2P2, and Ca5P8. Ca3P2 has the appearance of red-brown crystalline powder or grey lumps. Its trade name is Photophor for the incendiary use or Polytanol for the use as rodenticide. Preparation and structure It may be formed by reaction of the elements, but it is more commonly prepared by carbothermal reduction of calcium phosphate: :Ca3(PO4)2 + 8 C → Ca3P2 + 8 CO The structure of the room temperature form of Ca3P2 has not been confirmed by X-ray crystallography. A high temperature phase has been characterized by Rietveld refinement. Ca2+ centers are octahedral. Uses Metal phosphides are used as a rodenticide. A mixture of food and calcium phosphide is left where the rodents can eat it. The acid in the digestive system ...
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Gallium Phosphide
Gallium phosphide (GaP), a phosphide of gallium, is a compound semiconductor material with an indirect band gap of 2.24 eV at room temperature. Impure polycrystalline material has the appearance of pale orange or grayish pieces. Undoped single crystals are orange, but strongly doped wafers appear darker due to free-carrier absorption. It is odorless and insoluble in water. GaP has a microhardness of 9450 N/mm2, a Debye temperature of , and a thermal expansion coefficient of 5.3 K−1 at room temperature. Sulfur, silicon or tellurium are used as dopants to produce n-type semiconductors. Zinc is used as a dopant for the p-type semiconductor. Gallium phosphide has applications in optical systems. Its static dielectric constant is 11.1 at room temperature. Its refractive index varies between ~3.2 and 5.0 across the visible range, which is higher than in most other semiconducting materials. In its transparent range, its index is higher than almost any other transparent material, in ...
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Lithium Diphenylphosphide
Lithium diphenylphosphide contains lithium and the organophosphorus anion with the formula (C6H5)2PLi. It is an air-sensitive solid that is used in the preparation of diphenylphosphino compounds. As an ether complex, the lithium salt is dark red. Synthesis and reactions The lithium, sodium, and potassium salts are prepared by reduction of chlorodiphenylphosphine, triphenylphosphine, or tetraphenyldiphosphine with alkali metals (M): :(C6H5)2PCl + 2 M → (C6H5)2PM + MCl :(C6H5)3P + 2 M → (C6H5)2PM + MC6H5 :(C6H5)4P2 + 2 M → 2 (C6H5)2PM They can also be obtained by deprotonation of diphenylphosphine. With water, the salts convert to diphenylphosphine: :(C6H5)2PLi + H2O → (C6H5)2PH + LiOH With halocarbons, the salts react to give tertiary phosphines: :(C6H5)2PM + RX → (C6H5)2PR + MX When treated with metal halides, lithium diphenylphosphide gives transition metal phosphido complexes. Structure Although treated as salts, alkali diphe ...
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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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Schreibersite
Schreibersite is generally a rare iron nickel phosphide mineral, , though common in iron-nickel meteorites. It has been found on Disko Island in Greenland and Illinois. Another name used for the mineral is rhabdite. It forms tetragonal crystals with perfect 001 cleavage. Its color ranges from bronze to brass yellow to silver white. It has a density of 7.5 and a hardness of 6.5 – 7. It is opaque with a metallic luster and a dark gray streak. It was named after the Austrian scientist Carl Franz Anton Ritter von Schreibers (1775–1852), who was one of the first to describe it from iron meteorites.Schreibersite
Webmineral
Schreibersite is reported from the Magura Meteorite, Arva-(present name – Orava), Slovak Republic; the

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Arsenide
In chemistry, an arsenide is a compound of arsenic with a less electronegative element or elements. Many metals form binary compounds containing arsenic, and these are called arsenides. They exist with many stoichiometries, and in this respect arsenides are similar to phosphides. Alkali metal and alkaline earth arsenides The group 1 alkali metals and the group 2, alkaline earth metals, form arsenides with isolated arsenic atoms. They form upon heating arsenic powder with excess sodium gives sodium arsenide (Na3As). The structure of Na3As is complex with unusually short Na–Na distances of 328–330 pm which are shorter than in sodium metal. This short distance indicates the complex bonding in these simple phases, i.e. they are not simply salts of As3− anion, for example. The compound LiAs, has a metallic lustre and electrical conductivity indicating some metallic bonding. These compounds are mainly of academic interest. For example, "sodium arsenide" is a structural mo ...
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