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  2. Copper(I) iodide - Wikipedia

    en.wikipedia.org/wiki/Copper(I)_iodide

    Copper(I) iodide is white, but samples often appear tan or even, when found in nature as rare mineral marshite, reddish brown, but such color is due to the presence of impurities. It is common for samples of iodide-containing compounds to become discolored due to the facile aerobic oxidation of the iodide anion to molecular iodine. [4] [5] [6]

  3. List of copper salts - Wikipedia

    en.wikipedia.org/wiki/List_of_copper_salts

    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).

  4. Gilman reagent - Wikipedia

    en.wikipedia.org/wiki/Gilman_reagent

    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

  5. Category:Copper (I) compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Copper(I)_compounds

    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 ...

  6. Reactions of organocopper reagents - Wikipedia

    en.wikipedia.org/wiki/Reactions_of_organocopper...

    The addition of Grignard reagents to alkynes is facilitated by a catalytic amount of copper halide. Transmetalation to copper and carbocupration are followed by transmetalation of the product alkene back to magnesium. The addition is syn unless a coordinating group is nearby in the substrate, in which case the addition becomes anti and yields ...

  7. Ullmann condensation - Wikipedia

    en.wikipedia.org/wiki/Ullmann_condensation

    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.

  8. Phenylcopper - Wikipedia

    en.wikipedia.org/wiki/Phenylcopper

    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]

  9. Iodide - Wikipedia

    en.wikipedia.org/wiki/Iodide

    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 ...