Fluorine bonds

The bond dissociation energy of the hydrogen-fluorine bond in HF is so great that the above equilibrium lies to the left and hydrogen fluoride is a weak acid in dilute aqueous solution. In more concentrated solution, however, a second equilibrium reaction becomes important with the fluoride ion forming the complex ion HFJ. The relevant equilibria are ... 

The electrons in a carbon-fluorine bond are drawn away from carbon toward fluorine... 

Carbon-fluorine bonds are quite strong (slightly stronger than C—H bonds) and like polyethylene Teflon is a very stable inert material We are all familiar with the most characteristic property of Teflon its nonstick surface This can be understood by com paring Teflon and polyethylene The high electronegativity of fluorine makes C—P bonds less polarizable than C—H bonds causing the dispersion forces m Teflon to be less than those m polyethylene Thus the surface of Teflon is even less sticky than the already slick surface of polyethylene... 

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. 

Organic fluorine compounds were first prepared in the latter part of the nineteenth century. Pioneer work by the Belgian chemist, F. Swarts, led to observations that antimony(Ill) fluoride reacts with organic compounds having activated carbon—chlorine bonds to form the corresponding carbon—fluorine bonds. Preparation of fluorinated compounds was faciUtated by fluorinations with antimony(Ill) fluoride containing antimony(V) haUdes as a reaction catalyst. 

Substitution of fluorine for hydrogen in an organic compound has a profound influence on the compound s chemical and physical properties. Several factors that are characteristic of fluorine and that underHe the observed effects are the large electronegativity of fluorine, its small size, the low degree of polarizabiHty of the carbon—fluorine bond and the weak intermolecular forces. These effects are illustrated by the comparisons of properties of fluorocarbons to chlorocarbons and hydrocarbons in Tables 1 and 2. 

The principal advantage to this method is that the heat evolved for each carbon—fluorine bond formed, 192.5 kj/mol (46 kcal/mol), is much less than that obtained in direct fluorination, 435.3 kJ/mol (104 kcal/mol). The reaction yields are therefore much higher and less carbon—carbon bond scisson occurs. Only two metal fluorides are of practical use, Agp2 and GoF. ... 

Steric Factors. Initially, most of the coUisions of fluorine molecules with saturated or aromatic hydrocarbons occur at a hydrogen site or at a TT-bond (unsaturated) site. When coUision occurs at the TT-bond, the double bond disappears but the single bond remains because the energy released in initiation (eq. 4) is insufficient to fracture the carbon—carbon single bond. Once carbon—fluorine bonds have begun to form on the carbon skeleton of either an unsaturated or alkane system, the carbon skeleton is somewhat stericaUy protected by the sheath of fluorine atoms. Figure 2, which shows the crowded hehcal arrangement of fluorine around the carbon backbone of polytetrafluoroethylene (PTFE), is an example of an extreme case of steric protection of carbon—carbon bonds (29). 

C, which decomposes when heated above the melting point. Its solubility at 25°C in g/100 g solvent is water. 111 methanol, 5 ethanol, 1.4 acetone, 0.04 and carbon tetrachloride, 0.004. Because its carbon—fluorine bond is unreactive under most conditions, this salt can be converted by standard procedures to typical carboxylic acid derivatives such as fluoroacetyl esters (11,12), fluoroacetyl chloride [359-06-8] (13), fluoroacetamide (14), or fluoroacetonitrile [503-20-8] (14). 

Pyrolysis of chlorodifluoromethane is a noncatalytic gas-phase reaction carried out in a flow reactor at atmospheric or sub atmospheric pressure yields can be as high as 95% at 590—900°C. The economics of monomer production is highly dependent on the yields of this process. A significant amount of hydrogen chloride waste product is generated during the formation of the carbon—fluorine bonds. 

The presence of carbon—fluorine bonds in organic polymers is known to characteristically impart polymer stabiUty and solvent resistance. The poly(fluorosibcones) are siloxane polymers with fluorinated organic substituents bonded to siUcon. Poly(fluorosibcones) have unique appHcations resulting from the combination provided by fluorine substitution into a siloxane polymer stmcture (see Silicon compounds, silicones). 

The incorporation of a singlecarbon—fluorine bond into a polymer cannot provide the stabiUty and solvent resistance offered by multiple bonds or clusters ofcarbon—fluorine bonds available with substituents like the CF, 2 5 3 7 Therefore, commercially interesting po1y(fluorosi1icones)... 

When fluorine is beta to siUcon, compounds undergo a facile elimination of an ethylenic compound and again form the stable silicon—fluorine bond... 

The high thermal stability of the carbon-fluorine bond has led to considerable interest in fluorine-containing polymers as heat-resistant plastics and rubbers. The first patents, taken out by IG Farben in 1934, related to polychlorotri-fluoroethylene (PCTFE) (Figure 13.1 (a)), these materials being subsequently manufactured in Germany and the United States. PCTFE has been of limited application and it was the discovery of polytetrafluoroethylene (PTFE) (Figure... 

The carbon-fluorine bond is very stable. Further, where two fluorine atoms are attached to a single carbon atom there is a reduction in the C—F bond distance from 1.42 A to 1.35 A. As a result bond strengths may be as high as 504 kJ/mole. Since the only other bond present is the stable C—C bond, PTFE has a very high heat stability, even when heated above its crystalline melting point of 32TC. 

Polytetrafluoroethylene and fluorinated ethylene-propylene are the only resins composed wholly of fluorine and carbon. The polymer consists of fluorine atoms surrounding the carbon chain as a sheath, giving a chemically inert and relatively dense product from the strong carbon-fluorine bonds. Polytetrafluoroethylene must be molded at high pressure. Fluorinated ethylene-propylene c.m be injection molded and extruded as thin fdm. Both plastics have exceptional heat resistance... 

Filler, R Biochemistry Involving Carbon-Fluorine Bonds American Chemical Society Washington, DC 214... 

Methods for Synthesis of Organic Compounds Mth Nitrogen-Fluorine Bonding (Russ) Fokin A V Studnev, Y N, Kuznetsova, L G Reakt< Metndy h< led Org Soedm 24 7 66 819... 

The types of reactions covered in this segment are those in which the overall transformation is the conversion of a carbon-hydrogen bond to a carbon-fluorine bond through the use of electropositive fluorine reagents [7, 2, 3, 4, 5, 6]. 

Xenon difluoride fluorinates adamantane in low yield [45] (equation 22) When the carbon-hydrogen bond is activated by an a-sulfur atom, fliiorination occurs readily The reactions involve intermediates that contain sulfur-fluorine bonds. At-Fluoropyridinium reagents behave similarly [99, 100, 101, 102] (equations 55-57)... 

Esters of penta- and trivalentphosphorus acids and their derivatives readily undergo cleavage of the phosphorus-oxygen bond under extremely mild conditions with formation of the phosphorus-fluorine bond Phosphates and phosphi-... 

In contrast to phosphorus esters, sulfur esters are usually cleaved at the carbon-oxygen bond with carbon-fluorine bond formation Cleavage of esteri nf methanesulfonic acid, p-toluenesidfonic acid, and especially trifluoromethane-sulfonic acid (tnflic acid) by fluoride ion is the most widely used method for the conversion of hydroxy compounds to fluoro derivatives Potassium fluoride, triethylamine trihydrofluoride, and tetrabutylammonium fluoride are common sources of the fluoride ion For the cleavage of a variety of alkyl mesylates and tosylates with potassium fluoride, polyethylene glycol 400 is a solvent of choice, the yields are limited by solvolysis of the leaving group by the solvent, but this phenomenon is controlled by bulky substituents, either in the sulfonic acid part or in the alcohol part of the ester [42] (equation 29)... 

Huang, T J Dong, Z X, Shreeve, J M Inorg Chem 1987,26, 2604 Denson, D D, Uyemo, E T, Simon, R L, Peters, H M In Biochemistry Involving Carbon-Fluorine Bonds, Filler, R, Ed, ACS Symposium Se Ties 8, American Chemical Society Washington, DC, 1976 p 190 Van DerPuy, M 7 Fluorine Chem 1979,13 375 Shustov, L D, Nikolenko, L N, Senchenkova, T M Zh Obshch Khim 1983, 5i m.Chern Abstr 1983, 9S 143326v... 

Reductive removal of fluorme from alk I fluorides requires a potent reducing agent and so is not noimally encountered However, hydrogenolysis of an unacuvated carbon-fluorine bond in, for example, 3 (3-fluorocholestane has been efficiently accomplished in 88% yield with a solution of potassium and dicyclohexyl 18 crown-6 in toluene at 25 C [/] Similarly, sodium naphthaiene in tetrahydrofuran converts 6 tluorohexene-1 and 1-fluorohexane to hydrocarbons in 50% yield at 25 C over a 7-h penod [2]... 

The carbon-oxygen bond is strong, like the normal carbon-fluorine bond, it is difficult to reduce However, some structural features facilitate its reductive cleavage Aryl esters of perfluoroalkanesulfomc acids can be cleaved in good yield by... 

Hydrolytic cleavage of single carbon-fluorine bonds generally requires activation by a neighboring group such as a carbonyl, sulfonyloxy, or olefinic bond or a negatively substituted aromatic group. 

The insertion of calcium atoms into vinyl and aryl carbon-fluorine bonds has been reported Only the resulting organometallic from the aryl derivatives appears to live long enough to be trapped by water [J]... 

The last example represents a fairly rare elimination of hydrogen fluoride in preference to hydrogen chloride, a reaction that deserves a more detailed discussion A comparison of bond dissociation energies of carbon-halogen bonds shows that the carbon-fluorine bond is much stronger than the carbon-chlorine, carbon-bromine, and carbon-iodme bonds 108-116, 83 5, 70, and 56 kcal/mol, respec-... 

Guy, W S Taves, D R Brey, W S, Jr, In Biochemistry Involving Carbon-Fluorine Bonds Filler, R, Ed ACS Symposium Senes 28, Amencan Chemical Society, Washington, DC, 1976. 

COMPOUND BOND ELEMENT BONDED TO F FLUORINE BOND TYPE... 

The beryllium-fluorine bond is also highly ionic in character. However, there are two such Be-F bonds and the electrical properties of the entire molecule depend upon how these two bonds are oriented relative to each other. We must find the geometrical sum of these two bond dipoles. 

A very stable bond involving fluorine is the carbon-fluorine bond. The strength of this C—F bond is comparable to the C—H bond, and has led to the existence of a series of compounds known as the fluorocarbons. These are analogous to the hydrocarbons and can be imagined as being derived from them by substituting F atoms for H atoms. For example,... 

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