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This is an accepted version of this page This is the latest accepted revision, reviewed on 12 December 2024. This article is about the chemical element. For other uses, see Iodine (disambiguation). Chemical element with atomic number 53 (I) Iodine, 53 I Iodine Pronunciation / ˈ aɪ ə d aɪ n, - d ɪ n, - d iː n / (EYE -ə-dyne, -din, -deen) Appearance lustrous metallic gray solid ...
This application exploits the X-ray absorbing ability of the heavy iodine nucleus. A variety of agents are available commercially, many are derivatives of 1,3,5-triiodobenzene and contain about 50% by weight iodine. For most applications, the agent must be highly soluble in water and, of course, non-toxic and readily excreted.
By the same token, however, since iodine has the lowest ionisation energy among the halogens and is the most easily oxidised of them, it has a more significant cationic chemistry and its higher oxidation states are rather more stable than those of bromine and chlorine, for example in iodine heptafluoride. [1]
The PIDA molecule is termed hypervalent as its iodine atom (technically a hypervalent iodine) is in its +III oxidation state and has more than typical number of covalent bonds. [9] It adopts a T-shaped molecular geometry , with the phenyl group occupying one of the three equatorial positions of a trigonal bipyramid ( lone pairs occupy the other ...
The application of tincture of iodine may cause a rash. [citation needed] Some cases of reaction to povidone-iodine (Betadine) have been documented to be a chemical burn. [83] Medical use of iodine compounds (i.e. as a contrast agent) can cause anaphylactic shock in highly sensitive patients, presumably due to sensitivity to the chemical ...
In iodane chemistry, carbon is considered more electronegative than iodine, despite the Pauling electronegativities of those respective atoms. [2] Thus iodobenzene (C 6 H 5 I) is an iodine(I) compound, (dichloroiodo)benzene (C 6 H 5 ICl 2) and iodosobenzene (C 6 H 5 IO) iodine(III) compounds, and iodoxybenzene (C 6 H 5 IO 2) an iodine(V) compound.
Unlike tincture of iodine, Lugol's iodine has a minimised amount of the free iodine (I 2) component. Iodine glycerin, a preparation used in dentistry. Povidone iodine (an iodophor). Iodine-V: iodine (I 2) and fulvic acid form a clathrate compound (iodine molecules are "caged" by fulvic acid in this host-guest complex). A water-soluble, solid ...
The iodine clock reaction is a classical chemical clock demonstration experiment to display chemical kinetics in action; it was discovered by Hans Heinrich Landolt in 1886. [1] The iodine clock reaction exists in several variations, which each involve iodine species (iodide ion, free iodine, or iodate ion) and redox reagents in the presence of ...