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Selective fluorination

One of the earliest means of introducing fluorine selectively into specific positions of aromatic compounds is the Balz-Schiemann reaction [77] which dates back to the 1920s. An isolated arene diazonium tetrafluoroborate is thermolyzed at up to 120 °C to yield the corresponding fluoroaromatic compound. Because of the infamously hazardous nature of isolated diazonium salts the scope of the classical variant of the Balz-Schiemann reaction was limited to the small scale. The high exothermicity of the reaction is most conveniently controlled by diluting the diazonium salt with a solid inert medium such as sea sand. In addition to the danger to the experimenter, the reproducibility of the reaction yield is quite poor. [Pg.45]

Selective Electrochemical Fluorination, selective Electrochemical Fluorination, Scheme 11 Electrochemical fluorodesulfurization of Scheme 13 Solvent-free electrochemical fluorination dithioacetals using iodoarene mediator p-difluorobenzene in poly HE salt... [Pg.1872]

Choose the atoms of interest for the sem i-empirical calculation, then use the Bctend to sp option on the. Select menu to establish the appropriate atomic boundaries for the c uantnm mechanics calculation. TTyperChem substitutes pararmeteri/ed pseudo-fluorine atom s for th e portion s of the molecule n ot included directly in the calculation (see the second part of this book, Theory and Methods). [Pg.108]

The upper part of the figure illustrates why the small difference in mass between an ion and its neutral molecule is ignored for the purposes of mass spectrometry. In mass measurement, has been assigned arbitrarily to have a mass of 12.00000, All other atomic masses are referred to this standard. In the lower part of the figure, there is a small selection of elements with their naturally occurring isotopes and their natural abundances. At one extreme, xenon has nine naturally occurring isotopes, whereas, at the other, some elements such as fluorine have only one. [Pg.338]

Fluorine reacts with the halogens and antimony to produce several compounds of commercial importance antimony pentafluoride [7783-70-2J, bromine trifluoride [7787-71 chlorine trifluoride [7790-91 -2J, and iodine pentafluoride [7783-66-6J. Chlorine trifluoride is used in the processing of UF (see Uraniumand uranium compounds). Bromine trifluoride is used in chemical cutting by the oil well industry (see Petroleum). Antimony and iodine pentafluorides are used as selective fluorinating agents to produce fluorochemical intermediates (see Fluorine compounds, inorganic). [Pg.131]

Eluorspar assay may be completed by fluoride determination alone, because the mineralogical grouping rarely iacludes fluorine minerals other than fluorite. Calcium can be determined as oxalate or by ion-selective electrodes (67). SiUca can be determined ia the residue from solution ia perchloric acid—boric acid mixture by measuriag the loss ia weight on Aiming off with hydrofluoric acid. Another method for determining siUca ia fluorspar is the ASTM Standard Test Method E463-72. [Pg.175]

Iodine pentafluoride is an easily storable Hquid source of fluorine having Httie of the hazards associated with other fluorine sources. It is used as a selective fluorinating agent for organic compounds. For example, it adds iodine and fluorine to tetrafluoroethylene in a commercial process to produce a usefiil telomer (124). [Pg.187]

Mercury(II) fluoride has been used in the process for manufacture of fluoride glass (qv) for fiber optics (qv) appHcations (11) and in photochemical selective fluorination of organic substrates (12). It is available from Advance Research Chemicals, Aldrich Chemicals, Johnson/Matthey, Aesar, Cerac, Strem, and PCR in the United States. The 1993 annual consumption was less than 50 kg the price was 800—1000/kg. [Pg.210]

Uses. Silver fluoride has found many laboratory and special industrial appHcations. It is used as a soft (nHld) fluorinating agent for selective fluorination (7—17), as a cathode material in batteries (qv) (18), and as an antimicrobial agent (19). Silver fluoride is commercially available from Advance Research Chemicals, Inc., Aldrich Chemicals, Cerac Corp., Johnson/Matthey, PCR, Atochem, and other sources in the United States. The U.S. price of silver fluoride in 1993 was 1000— 1400/kg and the total U.S. consumption was less than 200 kg/yr. [Pg.235]

Fluorinated Heterocyclic Compounds. HeterocycHc compounds containing the CF group are prepared by methods similar to those used in the fluorination of aHphatic compounds. The direct action of fluorine on uracil yields the cancer chemotherapy agent, 5-fluorouracil [51-21-8] as one special example of a selective fluorination on a commercial scale (25). [Pg.269]

J. T. Welch, Selective Fluorination in Organic and Bioorganic Chemisty, ACS Symposium Senes 456, American Chemical Society, Washington, D.C., 1991. [Pg.272]

The high fluorine content contributes to resistance to attack by essentially all chemicals and oxidizing agents however, PCTFE does swell slightly ia halogenated compounds, ethers, esters, and selected aromatic solvents. Specific solvents should be tested. PCTFE has the lowest water-vapor transmission rate of any plastic (14,15), is impermeable to gases (see also Barrierpolymers), and does not carbonize or support combustion. [Pg.393]

Vluorosilicone. By fluorinating the siHcone polymer molecule it is possible to improve the solvent, fuel, and oil resistance of this already heat-resistant class of elastomers. The resulting polymers are especially useful in select automotive seals and gaskets as weU as military and downhole oilfield parts. [Pg.234]

Chlorine and fluorine in beryUium metal are isolated by pyrohydrolysis or by distUlation (21). Fluoride and chloride in the condensate are determined by ion-selective electrode or colorimetricaUy. [Pg.69]

The breadth of reactions catalyzed by cobalt compounds is large. Some types of reactions are hydrotreating petroleum (qv), hydrogenation, dehydrogenation, hydrodenitrification, hydrodesulfurization, selective oxidations, ammonoxidations, complete oxidations, hydroformylations, polymerizations, selective decompositions, ammonia (qv) synthesis, and fluorocarbon synthesis (see Fluorine compounds, organic). [Pg.380]


See other pages where Selective fluorination is mentioned: [Pg.61]    [Pg.61]    [Pg.2804]    [Pg.249]    [Pg.249]    [Pg.54]    [Pg.134]    [Pg.118]    [Pg.249]    [Pg.249]    [Pg.400]    [Pg.91]    [Pg.124]    [Pg.131]    [Pg.132]    [Pg.132]    [Pg.162]    [Pg.180]    [Pg.217]    [Pg.268]    [Pg.318]    [Pg.320]    [Pg.322]    [Pg.322]    [Pg.340]    [Pg.221]    [Pg.141]    [Pg.452]    [Pg.465]    [Pg.465]   
See also in sourсe #XX -- [ Pg.203 ]




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Fluorinated Ligands for Selective Catalytic Reactions

Fluorinated organic substances selective

Fluorinated steroids, biological selectivity

Fluorinations selective

Fluorine selected properties

Fluorine selective fluorination

Fluorine substitution, effect selectivities

Fluorine, elemental selective reactions

Fluorine-Deficient Discharges and Etch Rate Selectivity

Fluorine-induced adrenergic selectivities

Organic compounds selective fluorination

PARTIAL OR SELECTIVE FLUORINATION

Perfluorination and Selective Direct Fluorination

Potency and Selectivity by Introduction of Fluorine

Selected Fluorinated Structures and Reaction Types

Selection of fluorinated surfactants

Selective Direct Fluorination

Selective anodic fluorination

Selective anodic fluorination compounds

Selective anodic fluorination monofluorination

Selective anodic fluorination other

Selective anodic fluorination reaction

Selective anodic fluorination using fluorinating

Selective introduction of fluorine into

Selectivity in Radical Halogenation with Fluorine and Bromine

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