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Flourine atomic

When vinyl flouride is polymerized, a certain percentage of the flourine atoms are found on adjacent carbon atoms. When polyvinyl alcohol made by hydrolyzing polyvinyl acetate was treated with periodic acid by Flory, he found that the molecular weight was greatly reduced, indicating that there were 1,2-glycol units in the chain. But most of the polymers were regular head-to-tail polymers. [Pg.58]

Special attention should be paid to the fact that there is not the slightest indication in such a picture that one of the hydrogen atoms at IUPAC locant 8 is close enough to a flourine atom at locant ... [Pg.65]

Flamm, D.L. Donnelly, V.M. Mucha John, A. The reaction of flourine atoms with silicon. J. Appl. Phys. 1981, 52, 3633-3639. [Pg.2214]

Look up the isotopic composition of fluorine, atomic number 9, on the internet. Add the masses of the subatomic particles composing the flourine atom. Is the sum exactly that of the atomic mass given for F Should it be ... [Pg.132]

Similarly, BF molecule has zero dipole moment as also CH, CCl molecules. In all these cases, the individual dipole moments are all equal in magnitude and oriented in such a way that the net sum is zero. In BFj, the three flourine atoms are at the vertices of an equilateral triangle and the boron atom is at its center. In CH, the C atom is at the center of a regular tetrahedron while the four atoms bonded are at the vertices. [Pg.36]

Both molecules contain polcir covalent bonds based on electronegativity difference between the atoms. The C-F bonds of CF are slightly more polar than the H-0 bonds of water due to the greater difference in electronegativity between Ccirbon and flourine (1.5 versus 1.4), but the bonds are very close to being the same. [Pg.80]

The elements neon, argon, krypton, and xenon, the gases which are now used so much in electrical signs, all have no chemical properties. They do not form compounds with other elements. Their atomic numbers are 10, 18, 36, and 54, which are greater by unity than the numbers of flourine, chlorine, bromine, and iodine. [Pg.29]

Recently, Ojima et al. described the synthesis of some taxanes with C-13 fluorine-substituted isoserine side chains. In pharmaceutical practices, the fluorine atom is usually introduced as an isosteric atom of the hydrogen atom, but it showed higher or sometimes unique activity against its hydrogen-containing counterparts. Flourine also blocks the metabolism of the parent molecule, which led to the... [Pg.78]

In PET, radioactive substances that emit positrons are introduced into a patient s bloodstream. As the radioactive atoms decay, the positrons they emit collide with electrons, producing gamma rays that escape from the body and are detected by an array of instruments surrounding the patient. Computer analysis of the amount and direction of gamma ray production, and comparison of the data collected for people with and without certain brain disorders provides doctors with valuable information. For example, PET scans of the brain have been used to study the movement of the medication L-dopa in the brains of people suffering from Parkinson s disease. In these procedures, fluorine-18 atoms are attached to L-dopa molecules, which are then injected into a patient. Each flourine-18 decays and emits a positron that generates gamma rays when it meets an electron. [Pg.437]

Dichlorodifluoromethane. Black atoms are carbon turquoise atoms are flourine and green atoms are chlorine. Gray stick shows a double bond. [Pg.278]

Stannous flouride. Green atoms are tin and turquoise atom is flourine. publishers... [Pg.800]

The isomorphous replacements are of two kinds, (a) There are those replacements creating no negative charges as observed between the atoms of the same electrovalence and having no great difference in their ionic radii. Thus, Fe (ionic radius = r = 0.60 A) replaces A1 (r = 0.50 A), and Fe " (r = 0.75 A) replaces Mg r = 0.65 A). Similarly, the F ion often replaces the hydroxyls. Moreover, this replacement of hydroxyls by flourine can take place artificially (and reversibly) on the accessible hydroxyls of the surface of the particles (Hofmann [1956]). [Pg.103]


See other pages where Flourine atomic is mentioned: [Pg.514]    [Pg.89]    [Pg.514]    [Pg.514]    [Pg.89]    [Pg.514]    [Pg.431]    [Pg.441]    [Pg.302]    [Pg.127]    [Pg.340]    [Pg.1261]    [Pg.53]    [Pg.209]    [Pg.210]   
See also in sourсe #XX -- [ Pg.223 , Pg.228 , Pg.229 ]




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