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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).
Lithium dimethylcopper (CH 3) 2 CuLi can be prepared by adding copper(I) iodide to methyllithium in tetrahydrofuran at −78 °C. In the reaction depicted below, [4] the Gilman reagent is a methylating reagent reacting with an alkyne in a conjugate addition, and the ester group forms a cyclic enone. Scheme 1. Example Gilman reagent reaction
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
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A typical catalyst is formed from copper(I) iodide and phenanthroline. The reaction is an alternative to the Buchwald–Hartwig amination reaction. Aryl iodides are more reactive arylating agents than are aryl chlorides, following the usual pattern.
The low solubility of silver iodide and lead iodide reflects the covalent character of these metal iodides. A test for the presence of iodide ions is the formation of yellow precipitates of these compounds upon treatment of a solution of silver nitrate or lead(II) nitrate. [2] Aqueous solutions of iodide salts dissolve iodine better than pure ...
Fritz Ullmann and his student Bielecki were the first to report the reaction. [8] This groundbreaking result was the first to show that a transition metal could help perform an aryl carbon-carbon bond formation.