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The Wijs solution, iodine monochloride dissolved in acetic acid, is used to determine the iodine value of a substance. It can also be used to prepare iodates, by reaction with a chlorate. Chlorine is released as a byproduct. Iodine monochloride is a Lewis acid that forms 1:1 adducts with Lewis bases such as dimethylacetamide and benzene.
Iodine trichloride, which exists in the solid state as the planar dimer I 2 Cl 6, is a bright yellow solid, synthesised by reacting iodine with liquid chlorine at −80 °C; caution is necessary during purification because it easily dissociates to iodine monochloride and chlorine and hence can act as a strong chlorinating agent.
In 1886, German chemist Conrad Willgerodt prepared the first hypervalent iodine compound, iodobenzene dichloride (Ph I Cl 2), by passing chlorine gas through iodobenzene in a cooled solution of chloroform: [3] Ph I + Cl 2 → PhICl 2. This preparation can be varied to produce iodobenzene pseudohalides.
Such a triglyceride has a high iodine value (approx. 119). Below, the reaction product after the addition of four equivalents of iodine or bromine to the four C=C double bonds of the unsaturated fatty acid residues. The determination of iodine value is a particular example of iodometry. A solution of iodine I 2 is yellow/brown in
It is strongly oxidizing in acidic solution, less so in basic solution. When iodic acid acts as oxidizer, then the product of the reaction is either iodine, or iodide ion. Under some special conditions (very low pH and high concentration of chloride ions, such as in concentrated hydrochloric acid), iodic acid is reduced to iodine trichloride ...
Astatine monochloride [7] (AtCl) is made either by the direct combination of gas-phase astatine with chlorine or by the sequential addition of astatine and dichromate ion to an acidic chloride solution. Iodine monobromide (IBr) is made by the direct combination of the elements to form a dark red crystalline solid. It melts at 42 °C and boils ...
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.
An iodophor is a preparation containing iodine complexed with a solubilizing agent, such as a surfactant or water-soluble polymers such as povidone (forming povidone-iodine), [1] [2] The result is a water-soluble material that releases free iodine when in solution. Iodophors are prepared by mixing iodine with the solubilizing agent; heat can be ...