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Organic reactions catalysts

Ethylaluminum dichloride Ethylaluminum sesquichloride Tetrabutyl titanate Tetraisopropyl titanate Triethylborane Trimethylaluminum catalyst, olefin polymers Tungsten hexachloride catalyst, olefin/diene polymerizationscatalyst olefin polymerizations Tri-n-hexylaluminum catalyst, olefinic addition Methanesulfonic acid catalyst, one-component RTV s Dibutyltin diisooctylmaleate catalyst, organic compounds chlorination Manganese chloride (ous), tetrahydrate catalyst, organic reactions Beryllium oxide Chromium oxide (ic) Copper bromide (ous) Copper phosphate (ic) Ferric chloride... [Pg.4942]

In each case the configuration around the boron changes from trigonal planar to tetrahedral on adduct formation. Because of this ability to form additional compounds, boron trifluoride is an important catalyst and is used in many organic reactions, notably polymerisation, esterification, and Friedel-Crafts acylation and alkylations. [Pg.154]

The exchange resins 6nd application in (i) the purification of water (cation-exchange resin to remove salts, followed by anion-exchange resin to remove free mineral acids and carbonic acid), (ii) removal of inorganic impurities from organic substances, (iii) in the partial separation of amino acids, and (iv) as catalysts in organic reactions (e.g., esterification. Section 111,102, and cyanoethylation. Section VI,22). [Pg.1020]

Bcamples of metal-ion catalysed organic reactions in water where the catalyst acts exclusively as Lewis acid are the hromination of diketones" " and the decarboxylation of oxaloacetate. The latter reaction has been studied in detail. In 1941 it was demonstrated that magnesium(II) ions catalyse this reaction" Later also catalysis by other multivalent metal ions, such as Zn(II), Mn(II), Cu(II), Cd(ir), Fe(II), Pb(II), Fe(III)... [Pg.46]

First, the use of water limits the choice of Lewis-acid catalysts. The most active Lewis acids such as BFj, TiQ4 and AlClj react violently with water and cannot be used However, bivalent transition metal ions and trivalent lanthanide ions have proven to be active catalysts in aqueous solution for other organic reactions and are anticipated to be good candidates for the catalysis of aqueous Diels-Alder reactions. [Pg.48]

Boron trifluoride [7637-07-2] (trifluoroborane), BF, was first reported in 1809 by Gay-Lussac and Thenard (1) who prepared it by the reaction of boric acid and fluorspar at duU red heat. It is a colorless gas when dry, but fumes in the presence of moisture yielding a dense white smoke of irritating, pungent odor. It is widely used as an acid catalyst (2) for many types of organic reactions, especially for the production of polymer and petroleum (qv) products. The gas was first produced commercially in 1936 by the Harshaw Chemical Co. (see also Boron COMPOUNDS). [Pg.159]

Uses. Boron triduoride is an excellent Lewis acid catalyst for numerous types of organic reactions. Its advantages are ease of handling as a gas and the absence of undesirable tarry by-products. As an electrophilic molecule, it is an excellent catalyst for Friedel-Crafts and many other types of reactions (63-65) (see Friedel-craftsreactions). [Pg.162]

Resias are seldom used oace and discarded. Whether the system is mn batchwise or ia columns, the resia must be periodically removed from service and regenerated. An exception is the use of a resia as a catalyst ia organic reactions. Each cycle consists of two principal steps, adsorption and regeneration, and one or more iatermediate steps, tinse and backwash. Eailure to use good practices results ia poor cycHc performance. [Pg.383]

The green hexagonal crystals sublime above 1000°C. Iron(III) fluoride is slightly soluble ia water, freely soluble ia dilute HF, and nearly iasoluble ia alcohol, ether, and benzene. It is used as a catalyst ia organic reactions. [Pg.436]

Organic Reactions. Nitric acid is used extensively ia iadustry to nitrate aHphatic and aromatic compounds (21). In many iastances nitration requires the use of sulfuric acid as a dehydrating agent or catalyst the extent of nitration achieved depends on the concentration of nitric and sulfuric acids used. This is of iadustrial importance ia the manufacture of nitrobenzene and dinitrotoluene, which are iatermediates ia the manufacture of polyurethanes. Trinitrotoluene (TNT) is an explosive. Various isomers of mononitrotoluene are used to make optical brighteners, herbicides (qv), and iasecticides. Such nitrations are generally attributed to the presence of the nitronium ion, NO2, the concentration of which iacreases with acid strength (see Nitration). [Pg.39]

A. U. Blackham md J. Palmer, Technetium as a Catalyst in Organic Reactions, AT945-1-2017, Atimtic Richfield Hmford Co., Richlmd, Wash., July 1967. [Pg.208]

Rubidium-87 emits beta-particles and decomposes to strontium. The age of some rocks and minerals can be measured by the determination of the ratio of the mbidium isotope to the strontium isotope (see Radioisotopes). The technique has also been studied in dating human artifacts. Rubidium has also been used in photoelectric cells. Rubidium compounds act as catalysts in some organic reactions, although the use is mainly restricted to that of a cocatalyst. [Pg.281]

Barium acetate [543-80-6] Ba(C2H202)2, crystallines from an aqueous solution of acetic acid and barium carbonate or barium hydroxide. The level of hydration depends on crystallization temperature. At <24.7°C the trihydrate, density 2.02 g/mL is formed from 24.7 to 41 °C barium acetate monohydrate [5908-64-5] density 2.19 g/mL precipitates and above 41 °C the anhydrous salt, density 2.47 g/mL results. The monohydrate becomes anhydrous at 110°C. At 20°C, 76 g of the monohydrate dissolves in 100 g of water. Barium acetate is used in printing fabrics, lubricating grease, and as a catalyst for organic reactions. [Pg.476]

Boric oxide is used as a catalyst ia many organic reactions. It also serves as an iatermediate ia the production of boron haUdes, esters, carbide, nitride, and metallic borides. [Pg.191]

Aqueous solutions have low conductivities resulting from extensive complex ion formation. The haUdes, along with the chalcogenides, are sometimes used in pyrotechnics to give blue flames and as catalysts for a number of organic reactions. [Pg.394]

Phase-tiansfei catalysis (PTC) is a technique by which leactions between substances located in diffeient phases aie biought about oi accelerated. Typically, one OI more of the reactants are organic Hquids or soHds dissolved in a nonpolar organic solvent and the coreactants are salts or alkah metal hydroxides in aqueous solution. Without a catalyst such reactions are often slow or do not occur at ah the phase-transfer catalyst, however, makes such conversions fast and efficient. Catalysts used most extensively are quaternary ammonium or phosphonium salts, and crown ethers and cryptates. Although isolated examples of PTC can be found in the early Hterature, it is only since the middle of the 1960s that the method has developed extensively. [Pg.186]

Many reactions can be carried out between potassium cyanide and organic compounds with the alkalinity of the KCN acting as a catalyst these reactions are analogous to reactions of sodium cyanide. The reactions of potassium cyanide with sulfur and sulfur compounds are also analogous to those of sodium cyanide. Potassium cyanide is reduced to potassium metal and carbon by heating it out of contact with air in the presence of powdered magnesium. Magnesium is converted to the nitride ... [Pg.385]

Lewis acids are defined as molecules that act as electron-pair acceptors. The proton is an important special case, but many other species can play an important role in the catalysis of organic reactions. The most important in organic reactions are metal cations and covalent compounds of metals. Metal cations that play prominent roles as catalysts include the alkali-metal monocations Li+, Na+, K+, Cs+, and Rb+, divalent ions such as Mg +, Ca +, and Zn, marry of the transition-metal cations, and certain lanthanides. The most commonly employed of the covalent compounds include boron trifluoride, aluminum chloride, titanium tetrachloride, and tin tetrachloride. Various other derivatives of boron, aluminum, and titanium also are employed as Lewis acid catalysts. [Pg.233]

Covalent fluondes of group 3 and group 5 elements (boron, tin, phosphorus, antimony, etc ) are widely used m organic synthesis as strong Lewis acids Boron trifluoride etherate is one of the most common reagents used to catalyze many organic reactions. A representative example is its recent application as a catalyst in the cycloadditions of 2-aza-l,3-dienes with different dienophiles [14] Boron trifluoride etherate and other fluonnated Lewis acids are effective activators of the... [Pg.944]

Hydrotreating Technology for Pollution Control Catalysts, Catalysis, and Processes, edited by Mario L. Occelli and Russell Chianelli Catalysis of Organic Reactions, edited by Russell E. Malz, Jr. [Pg.675]

We had no good way to predict if they would be liquid, but we were lucky that many were. The class of cations that were the most attractive candidates was that of the dialkylimidazolium salts, and our particular favorite was l-ethyl-3-methylimid-azolium [EMIM]. [EMIMJCl mixed with AICI3 made ionic liquids with melting temperatures below room temperature over a wide range of compositions [8]. We determined chemical and physical properties once again, and demonstrated some new battery concepts based on this well behaved new electrolyte. We and others also tried some organic reactions, such as Eriedel-Crafts chemistry, and found the ionic liquids to be excellent both as solvents and as catalysts [9]. It appeared to act like acetonitrile, except that is was totally ionic and nonvolatile. [Pg.5]

Acidic chloroaluminate ionic liquids have already been described as both solvents and catalysts for reactions conventionally catalyzed by AICI3, such as catalytic Friedel-Crafts alkylation [35] or stoichiometric Friedel-Crafts acylation [36], in Section 5.1. In a very similar manner, Lewis-acidic transition metal complexes can form complex anions by reaction with organic halide salts. Seddon and co-workers, for example, patented a Friedel-Crafts acylation process based on an acidic chloro-ferrate ionic liquid catalyst [37]. [Pg.225]

Other possibilities for practical application of resin catalysis include some organic reactions involving addition, cyclization, and structural rearrangement. Increased stability and specific control of structure has led to the increased use of cation exchange resins as catalysts. As in the case of cation exchange resins many... [Pg.775]


See other pages where Organic reactions catalysts is mentioned: [Pg.111]    [Pg.111]    [Pg.44]    [Pg.101]    [Pg.164]    [Pg.177]    [Pg.230]    [Pg.436]    [Pg.14]    [Pg.38]    [Pg.337]    [Pg.169]    [Pg.95]    [Pg.161]    [Pg.222]    [Pg.292]    [Pg.292]    [Pg.396]    [Pg.100]    [Pg.673]    [Pg.1114]    [Pg.565]    [Pg.57]    [Pg.245]    [Pg.260]    [Pg.266]    [Pg.353]    [Pg.230]   
See also in sourсe #XX -- [ Pg.563 ]

See also in sourсe #XX -- [ Pg.596 ]

See also in sourсe #XX -- [ Pg.563 ]

See also in sourсe #XX -- [ Pg.563 ]

See also in sourсe #XX -- [ Pg.563 ]




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