Fluoride number

Alternative nomenclature Alternative nomenclature Relative Dibucaine activity number Fluoride number ... 

Two other pairs of tubes are prepared to determine the percentage of inhibition by dibucaine (concentration in reaction mixture 0.03 mmol/liter) and by sodium fluoride (concentration in reaction mixture 4 mmol/liter). In each case one out of the pair of tubes serves as the blank. The inhibitor is added to all tubes with the substrate. The remainder of the assay procedure is identical to that of the uninhibited reaction. The percentages of inhibition by dibucaine (dibucaine number) and by fluoride (fluoride number) are calculated as described in Section 6.3.2.2. 

Normal cholinesterase is inhibited to a large extent by fluoride (i.e. it has a high fluoride number). In individuals with suxamethonium sensitivity, the cholinesterase differs from the normal form and it is less susceptible to inhibition (i.e. has lower fluoride numbers). This fact can be used in phenotyping members of an affected family since heterozygotes have fluoride numbers intermediate between those of normals and homozygotes. 

From the tables it is clear that elements in Groups I-IV can display a valency equal to the group number. In Groups V-VII. however, a group valency equal to the group number (x) can be shown in the oxides and fluorides (except chlorine) but a lower valency (8 — x) is displayed in the hydrides. This lower valency (8 — x) is also found in compounds of the head elements of Groups V-VII. 

The melting and boiling points of the aluminium halides, in contrast to the boron compounds, are irregular. It might reasonably be expected that aluminium, being a more metallic element than boron, would form an ionic fluoride and indeed the fact that it remains solid until 1564 K. when it sublimes, would tend to confirm this, although it should not be concluded that the fluoride is, therefore, wholly ionic. The crystal structure is such that each aluminium has a coordination number of six, being surrounded by six fluoride ions. 

One hypothesis says that fluorine can be substituted for hydrogen wherever it occurs in organic compounds, which could lead to an astronomical number of new fluorine compounds. Compounds of fluorine with rare gases have now been confirmed in fluorides of xenon, radon, and krypton. 

Gr. aktis, aktinos, beam or ray). Discovered by Andre Debierne in 1899 and independently by F. Giesel in 1902. Occurs naturally in association with uranium minerals. Actinium-227, a decay product of uranium-235, is a beta emitter with a 21.6-year half-life. Its principal decay products are thorium-227 (18.5-day half-life), radium-223 (11.4-day half-life), and a number of short-lived products including radon, bismuth, polonium, and lead isotopes. In equilibrium with its decay products, it is a powerful source of alpha rays. Actinium metal has been prepared by the reduction of actinium fluoride with lithium vapor at about 1100 to 1300-degrees G. The chemical behavior of actinium is similar to that of the rare earths, particularly lanthanum. Purified actinium comes into equilibrium with its decay products at the end of 185 days, and then decays according to its 21.6-year half-life. It is about 150 times as active as radium, making it of value in the production of neutrons. 

We also developed a number of other useful new fluorinating reagents. They ineluded a convenient in situ form of sulfur tetrafluoride in pyridinium polyhydrogen fluoride, selenium tetrafluoride, and ey-anurie fluoride. We introdueed uranium hexafluoride (UFg), depleted from the U-235 isotope, which is an abundant by-product of enrichment plants, as an effective fluorinating agent. 

Fluorine is the most electronegative element and thus can oxidize many other elements to their highest oxidation state. The small size of the fluorine atom facihtates the arrangement of a large number of fluorines around an atom of another element. These properties of high oxidation potential and small size allow the formation of many simple and complex fluorides in which the other elements are at their highest oxidation states. 

The fluoride ion is the least polarizable anion. It is small, having a diameter of 0.136 nm, 0.045 nm smaller than the chloride ion. The isoelectronic E and ions are the only anions of comparable size to many cations. These anions are about the same size as K" and Ba " and smaller than Rb" and Cs". The small size of E allows for high coordination numbers and leads to different crystal forms and solubiUties, and higher bond energies than are evidenced by the other haUdes. Bonds between fluorine and other elements are strong whereas the fluorine—fluorine bond is much weaker, 158.8 kj/mol (37.95 kcal/mol), than the chlorine—chlorine bond which is 242.58 kJ/mol (57.98 kcal/mol). This bond weakness relative to the second-row elements is also seen ia 0-0 and N—N single bonds and results from electronic repulsion. 

Uranium is converted by CIF, BiF, and BrP to UF. The recovery of uranium from irradiated fuels has been the subject of numerous and extensive investigations sponsored by atomic energy agencies in a number of countries (55—63). The fluorides of the nuclear fission products are nonvolatile hence the volatile UF can be removed by distiUation (see Nuclearreactors Uraniumand uranium compounds). 

Specifications, Shipping, and Analysis. Hydrogen fluoride is shipped in bulk in tank cars (specification 112S400W) and tank tmcks (specification MC312). A small volume of overseas business is shipped in ISO tanks. Bulk shipments are made of anhydrous HF as well as 70% aqueous solutions. A small amount of aqueous solution may be shipped as 50%. Cars and tmcks used for anhydrous HF transport are of carbon steel constmction. It is possible to ship 70% aqueous in steel from a corrosion standpoint however, mbber lining is commonly used to eliminate iron pickup, which is detrimental to product quaUty in a number of appHcations. Hydrogen fluoride of less than 60% strength must always be shipped in lined containers. 

A number of fluorides have beea showa to form 0" 2 compouads upoa reactioa with O2F2. 

HFPO reacts with a large number of acyl fluorides in a general reaction to give 2-alkoxytettafluotoptopionyl fluorides which in turn may be converted to trifluorovinyl ethers (eq. 14). 

Iron hahdes react with haHde salts to afford anionic haHde complexes. Because kon(III) is a hard acid, the complexes that it forms are most stable with F and decrease ki both coordination number and stabiHty with heavier haHdes. No stable F complexes are known. [FeF (H20)] is the predominant kon fluoride species ki aqueous solution. The [FeF ] ion can be prepared ki fused salts. Whereas six-coordinate [FeCy is known, four-coordinate complexes are favored for chloride. Salts of tetrahedral [FeCfy] can be isolated if large cations such as tetraphenfyarsonium or tetra alkylammonium are used. [FeBrJ is known but is thermally unstable and disproportionates to kon(II) and bromine. Complex anions of kon(II) hahdes are less common. [FeCfy] has been obtained from FeCfy by reaction with alkaH metal chlorides ki the melt or with tetraethyl ammonium chloride ki deoxygenated ethanol. 

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