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A Boron

Methods of producing B —C bonds include hydroboration, nucleophilic displacement at a boron atom in BX., (X = halogens or B(0R>3) by e.g. a Grignard reagent, and a psewiio-Friedel-Crafts reaction with an aromatic hydrocarbon, BX3, and AICI3. [Pg.289]

Hydroboration is a reaction m which a boron hydride a compound of the type R2BH adds to a carbon-carbon bond A carbon-hydrogen bond and a carbon-boron bond result... [Pg.250]

The 4 point group is that to which a regular icosahedron, illustrated in Figure 4.13(a), belongs. It contains 20 equilateral triangles arranged in a three-dimensional sttucture. This is the conformation of the anion, in which there is a boron atom, with a hydrogen atom... [Pg.86]

Other forms of carbon-carbon composites have been or are being developed for space shutde leading edges, nuclear fuel containers for sateUites, aircraft engine adjustable exhaust nozzles, and the main stmcture for the proposed National Aerospace plane (34). For reusable appHcations, a siHcon carbide [409-21 -2] based coating is added to retard oxidation (35,36), with a boron [7440-42-8] h Lsed sublayer to seal any cracks that may form in the coating. [Pg.5]

Ammonium Fluoroborate. Ammonium fluoroborate [13826-83-0] NH BF, is unique in that when it is exposed to a flame, it generates both a halogen and a boron flame retardant (20). Antimony oxide is usually recommended as a co-synergist. [Pg.457]

Manufacture. Boron trifluoride is prepared by the reaction of a boron-containing material and a fluorine-containing substance in the presence of an acid. The traditional method used borax, fluorspar, and sulfuric acid. [Pg.161]

Hydroboration is the addition of a boron—hydrogenbond across a double or triple carbon—carbon bond to give an organoborane ... [Pg.308]

R. Thompson and A. J. E. Welch, eds., Me//or s Comprehensive Treatise on Inorganic and Theoretical Chemist, Vol. V, Boron, Part A, Boron-Oypigen Compounds, Longman, New York, London, 1980. [Pg.209]

Each boron atom is bonded to five others ia the icosahedron as well as either to a carbon atom or to a boron atom ia an adjacent icosahedron. The stmcture is similar to that of rhombohedral boron (see Boron, elemental). The theoretical density for B22C2 is 2.52 g/mL. The rigid framework of... [Pg.219]

When a boron atom of a borane is replaced by a heteroelement, the compounds are called carbaboranes, phosphaboranes, thiaboranes, a2aboranes, etc, by an adaptation of organic replacement nomenclature. The numbering of the skeleton in heteroboranes is such that the heteroelement is given the lowest possible number consistent with the conventions of the parent borane. Thus C2B2H is dicarba- /(9j (9-pentaborane(5) and could occur as the 1,2-, 2,3-, or 1,5-isomeric forms (l,2-dicarba- /(9j (9-pentaborane(5) [23777-70-0] 2,3-dicarba- /(9j (9-pentaborane(5) [30396-61-3] and... [Pg.228]

Aromatic Aldehydes. Carbon monoxide reacts with aromatic hydrocarbons or aryl haHdes to yield aromatic aldehydes (see Aldehydes). The reaction of equation 24 proceeds with yields of 89% when carried out at 273 K and 0.4 MPa (4 atm) using a boron trifluoride—hydrogen fluoride catalyst (72), whereas conversion of aryl haHdes to aldehydes in 84% yield by reaction with CO + H2 requires conditions of 423 K and 7 MPa (70 atm) with a homogeneous palladium catalyst (73) and also produces HCl. [Pg.53]

Another type of anion, confined for practical purposes to boron compounds, has no unshared electrons at the anionic site, and must be thought of as being formed by addition of hydride to a boron atom (or other atom with an incomplete valence shell). Such structures were not anticipated at the time general heterocyclic nomenclature was developed, and they are only recently being fitted into systematic nomenclature (lUPAC Provisional Recommendation 83.2). Proposals for a suffix to indicate such structures are under consideration (1982). [Pg.44]

Dichlorodicyanoquinone (DDQ), CH2CI2, H2O, 40 min, it, 84-93% yield.This method does not cleave simple benzyl ethers. This method was found effective in the presence of a boronate. The following groups are stable to these conditions ketones, epoxides, alkenes, acetonides, to-sylates, MOM ethers, THP ethers, acetates, benzyloxymethyl (BOM) ethers, and TBDMS ethers. [Pg.54]

When the structure of a metal changes, it is because there is a driving force for the change. When iron goes from b.c.c. to f.c.c. as it is heated, or when a boron dopant diffuses into a silicon semiconductor, or when a powdered superalloy sinters together, it is because each process is pushed along by a driving force. [Pg.46]

Figure 3a Unprocessed depth profile (secondary ion intensity versus sputtering time) of a silicon sample containing a boron ion implant. Figure 3a Unprocessed depth profile (secondary ion intensity versus sputtering time) of a silicon sample containing a boron ion implant.
In a typical process adiponitrile is formed by the interaction of adipic acid and gaseous ammonia in the presence of a boron phosphate catalyst at 305-350°C. The adiponitrile is purified and then subjected to continuous hydrogenation at 130°C and 4000 Ibf/in (28 MPa) pressure in the presence of excess ammonia and a cobalt catalyst. By-products such as hexamethyleneimine are formed but the quantity produced is minimized by the use of excess ammonia. Pure hexamethylenediamine (boiling point 90-92°C at 14mmHg pressure, melting point 39°C) is obtained by distillation, Hexamethylenediamine is also prepared commercially from butadience. The butadiene feedstock is of relatively low cost but it does use substantial quantities of hydrogen cyanide. The process developed by Du Pont may be given schematically as ... [Pg.481]

As a second example, results from a TOP ERDA measurement for a multi-element sample are shown in Fig. 3.65 [3.171]. The sample consists of different metal-metal oxide layers on a boron silicate glass. The projectiles are 120-MeV Kr ions. It can be seen that many different recoil ions can be separated from the most intense line, produced by the scattered projectiles. Figure 3.66 shows the energy spectra for O and Al recoils calculated from the measured TOF spectra, together with simulated spectra using the SIMNRA code. The concentration and thickness of the O and Al layers are obtained from the simulations. [Pg.169]

A scram causes the control rods to drop into the core, absorb neutrons and stop the chain reaction. Some rods perform both controlling and scram functions. The control rods are raised to increase the neutron flux (and power) or lowered to reduce it by magnetic jacks (W and CE) or a magnetic "clamshell" screw (B W). The chemical volume and control system (CVCS - not siiown) controls the water quality, removes radioactivity, and varies the reactivity by controUing the amount of a boron compound that is dissolved in the water - called a "poison." Thus, a PWR coiiirols reactivity two ways by the amount of poison in the water and by moving the control rods. [Pg.208]

Figure 3-37 E2 Calculations for a Boron-Epoxy Composite Material (After Halplrt and Tsai [3-17])... Figure 3-37 E2 Calculations for a Boron-Epoxy Composite Material (After Halplrt and Tsai [3-17])...
Let s address the issue of nonlinear material behavior, i.e., nonlinear stress-strain behavior. Where does this nonlinear material behavior come from Generally, any of the matrix-dominated properties will exhibit some degree of material nonlinearity because a matrix material is generally a plastic material, such as a resin or even a metal in a metal-matrix composite. For example, in a boron-aluminum composite material, recognize that the aluminum matrix is a metal with an inherently nonlinear stress-strain curve. Thus, the matrix-dominated properties, 3 and Gj2i generally have some level of nonlinear stress-strain curve. [Pg.458]

Alkyl silyl ethers are cleaved by a variety of reagents Whether the silicon-oxygen or the carbon-oxygen bond is cleaved depends on the nature of the reagent used Treatment of alkoxysilanes with electrophilic reagents like antimony tri-fluonde, 40% hydrofluonc acid, or a boron tnfluonde-ether complex results in the cleavage of the silicon-oxygen bond to form mono-, di-, and tnfluorosiloxanes or silanes [19, 20, 21) (equations 18-20)... [Pg.205]

With this as introduction, let us now look at the individual steps in more detail for the case of hydroboration-oxidation of 1-decene. A boron hydride that is often used is dibomne (B2H6). Diborane adds to 1-decene to give tridecylborane according to the balanced equation ... [Pg.251]

The main chemical products produced from these minerals are (a) boron oxides, boric acid and borates, (b) esters of boric acid, (c) refractory boron compounds (borides, eu .), (d) boron halides, (e) boranes and carbaboranes and (f) organoboranes. The main industrial and domestic uses of boron compounds in Europe (USA in parentheses) are ... [Pg.140]

Figure 6.10 Cubic MBs showing (a) boron octahedra (B-B in range 170-174 pm), and (b) 24-atom coordination polyhedron around each metal atom. Figure 6.10 Cubic MBs showing (a) boron octahedra (B-B in range 170-174 pm), and (b) 24-atom coordination polyhedron around each metal atom.

See other pages where A Boron is mentioned: [Pg.115]    [Pg.1218]    [Pg.32]    [Pg.251]    [Pg.78]    [Pg.344]    [Pg.314]    [Pg.245]    [Pg.136]    [Pg.201]    [Pg.92]    [Pg.247]    [Pg.141]    [Pg.222]    [Pg.411]    [Pg.259]    [Pg.6]    [Pg.538]    [Pg.71]    [Pg.39]    [Pg.81]    [Pg.121]    [Pg.311]    [Pg.32]    [Pg.55]   


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A Brief History of Boronic Ester Chemistry

A DETERMINATION OF BORON BY SPECTROPHOTOMETRY

A Species Containing Trigonal Boron

A Topological Theory of Boron Hydrides

A boron analogues

A form of boron nitride

A-Halo boronic acids

A-allenic boronic esters

Applications of Boron Nitride as a Solid Lubricant and Separating Medium

Boron Heterocycles as Ligands in Transition-Metal Chemistry

Boron as Lewis Acid Catalysts

Boron as plant nutrient

Boron as reactant

Boron compounds, allylconfigurational stability reactions with chiral a-methyl aldehydes

Boron compounds, as fire retardants

Boron compounds, crotylreactions with chiral a-methyl aldehydes

Boron heterocycles as ligands

Boron trifluoride as catalyst

Boron trifluoride ketone a-acetoxylation

Boron trifluoride, as Lewis acid

Boron, transition metal nanoparticles as catalyst borane

Boronic Acid Functionalized Viologens as Saccharide Sensors

Boronic Esters as Enzyme Inhibitors

Boronic acid, a-chloroallylmismatched diastereoselective reactions with

Boronic acid, a-chloroallylmismatched diastereoselective reactions with aldehydes

Boronic acid, a-chlorocrotyldiastereofacial preference

Boronic acid, a-chlorocrotyldiastereofacial preference reactions with aldehydes

Boronic acid, a-methoxycrotylmismatched double diastereoselectivity

Boronic acid, a-methylcrotylreaction with benzaldehyde

Boronic acid, allylesters reactions with a-methyl chiral aldehydes

Boronic acid-Nucleophile Complex Formed in the Enzyme Active Site as a way to Improve Potency and Selectivity

Chemical Reactivity of the Boron F. G. A. Stone

Chloroacetoxylation a-Chloroalkyl) boronic esters

Deposition by d.c. Magnetron Sputter with a Hot Boron Target

Formation of Exopolyhedral a Bonds between Cage Boron Atoms and Transition Elements

Free Radicals from (a-Haloalkyl)boronic Esters

Hexagonal Boron Nitride with Graphite-Type Structure (a-BN) and Other Structures of Normal Density

Hexagonal a-Boron Nitride

Ketones, a-phenylthio via acylation of boron-stabilized carbanions

Metal Substitutions of (a-Haloalkyl)boronic Esters

Other Aspects of (a-Chloroalkyl)boronic Ester Chemistry

Physical Adsorption on Hexagonal Graphitic Boron Nitride (a-BN)

Sadimenko, A. P., Organometallic Complexes of Boron, Silicon, and

The Subhalides of Boron A. G. Massey

W-Halo-acids a-Haloalkyl) boronic ester

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