Search results
Results from the WOW.Com Content Network
Copper(I) iodide reacts with mercury vapors to form brown copper(I) tetraiodomercurate(II): 4 CuI + Hg → (Cu +) 2 [HgI 4] 2− + 2 Cu. This reaction can be used for the detection of mercury since the white CuI to brown Cu 2 [HgI 4] color change is dramatic. Copper(I) iodide is used in the synthesis of Cu(I) clusters such as [Cu 6 I 7] −. [10]
Copper is a chemical element with the symbol Cu (from Latin: cuprum) and the atomic number of 29. It is easily recognisable, due to its distinct red-orange color.Copper also has a range of different organic and inorganic salts, having varying oxidation states ranging from (0,I) to (III).
Iodometry is commonly employed to determine the active amount of hypochlorite in bleach responsible for the bleaching action. In this method, excess but known amount of iodide is added to known volume of sample, in which only the active (electrophilic) can oxidize iodide to iodine. The iodine content and thus the active chlorine content can be ...
Phenylcopper was the first known organocopper compound and was first prepared in 1923 from phenylmagnesium iodide and copper(I) iodide and in 1936 by Henry Gilman by transmetallation of phenylmagnesium iodide with copper(I) chloride. Phenylcopper can be obtained by reacting phenyl lithium with copper(I) bromide in diethyl ether. [3]
Some copper proteins form oxo complexes, which also feature copper(III). [20] With tetrapeptides, purple-colored copper(III) complexes are stabilized by the deprotonated amide ligands. [21] Complexes of copper(III) are also found as intermediates in reactions of organocopper compounds. [22] For example, in the Kharasch–Sosnovsky reaction.
Copper hydride; Copper indium gallium selenide; Copper oxide selenite; Copper(I) acetylide; Copper(I) bromide; Copper(I) chloride; Copper(I) cyanide; Copper(I) fluoride; Copper(I) hydroxide; Copper(I) iodide; Copper(I) nitrate; Copper(I) oxide; Copper(I) phosphide; Copper(I) sulfate; Copper(I) sulfide; Copper(I) telluride; Copper(I) tert ...
The aromatic chlorides and bromides are not easily substituted by iodide, though they may occur when appropriately catalyzed. The so-called "aromatic Finkelstein reaction" is catalyzed by copper(I) iodide in combination with diamine ligands. [9] Nickel bromide and tri-n-butylphosphine have been found to be suitable catalysts as well. [10]
This page was last edited on 10 January 2009, at 17:28 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.