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Iron(iii) Chloride Iron(III) chloride (also called ferric chloride) is an iron-based salt of chemical formula FeCl3). It is very hygroscopic and it fumes in moist air with hydrolysis and when dissolved in water, it evolves a great deal of heat and produces a brown, foul-smelling, acidic solution. This corrosive liquid is used to etch copper-based metals (such as those found in electrical circuit boards) and stainless steel and in treating sewage and drinking water. Anhydrous iron(III) chloride is a fairly strong Lewis acid, and it is used as a catalyst in organic synthesis. The brownish-yellow hexahydrate is a common commercial form of FeCl3 which in fact has the structure FeCl2(H2O)4Cl.2H2O (compare chromium(III) chloride). When heated, FeCl3 melts then boils at around 315 C. The vapour contains dimers of Fe2Cl6 (compare aluminium chloride) which slowly decompose to give FeCl2 and Cl2. Chemical properties Iron(III) chloride is a moderately strong Lewis acid which with Lewis bases such as triphenylphosphine oxide forms stable adducts such as FeCl3(OPPh3)2 where Ph = phenyl. With chloride ion several anionic complexes are known, but the most stable contain the yellow tetrahedral FeCl4- ion. Solutions of FeCl4- in hydrochloric acid may be extracted into diethyl ether. When heated with iron(III) oxide at 350 C the oxychloride FeOCl is formed. In the presence of base, iron(III) chloride may undergo replacement of chloride, for example to produce an alkoxide: FeCl3 + 3 C2H5OH + 3 NH3 → Fe(OC2H5)3 + 3 NH4Cl Carboxylate salts such as oxalate, citrate or tartrate react easily with aqueous FeCl3 to form stable complexes such as Fe(C2O4)33-. Iron(III) chloride is also a mild oxidising agent, capable (for example) of oxidising copper(I) chloride to copper(II) chloride. Reducing agents such as hydrazine cause reduction of FeCl3 to complexes of iron(II). Preparation Anhydrous iron(III) chloride may be prepared by union of the elements: 2 Fe(s) + 3 Cl2(g) → 2 FeCl3(s) Note that FeCl3 can not be prepared from iron and hydrochloric acid, as this instead forms iron(II) chloride. Hydrated FeCl3 can be dehydrated to the anhydrous salt by heating with thionyl chloride. The hydrated salt itself may be made by the action of hydrochloric acid on FeO(OH). Uses Iron(III) chloride is probably the most widely etching material1. It is commonly used for etching copper in the production of printed circuit boards. This occurs by the redox reaction FeCl3 + Cu → FeCl2 + CuCl followed by FeCl3 + CuCl → FeCl2 + CuCl2 Iron(III) chloride is also used as a catalyst for the reaction of ethylene with chlorine. This is used for the industrial production of vinyl chloride, the monomer for making PVC. A related reaction is also used for making 1,2-dichloroethane, an important commodity chemical. Another industrial application is an alternative to iron(III) sulfate in water treatment, where FeCl3 is treated with hydroxide ion to form a floc of "iron(III) hydroxide" (more correctly formulated as FeO(OH)) that can remove suspended materials. In the laboratory iron(III) chloride is most commonly used as a Lewis acid for catalysing reactions such as chlorination of aromatic compounds and Friedel-Crafts reaction of aromatics. It is less powerful than aluminium chloride, but in some cases this mildness leads to higher yields, for example in the alkylation of benzene: 400px The "ferric chloride test" is a traditional colorimetric test for phenols7 which uses a 1% iron(III) chloride solution that has been neutralised with sodium hydroxide until a slight precipitate of FeO(OH) is formed. The mixture is filtered before use. The organic substance is dissolved in water, methanol or ethanol, then the neutralised FeCl3 solution is added- a transient or permanent coloration (usually purple, green or blue) indicates the presence of a phenol or enol. FeCl3 is sometimes used by American coin collectors to identify the dates of Buffalo nickels that are so badly worn that the date is no longer visible. Precautions Iron(III) chloride is toxic, highly corrosive and acidic. The anhydrous material is a powerful dehydrating agent. Suppliers/Manufacturers References - N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth-Heinemann, Oxford, UK, 1997.
- Handbook of Chemistry and Physics, 71st edition, CRC Press, Ann Arbor, Michigan, 1990.
- The Merck Index, 7th edition, Merck & Co, Rahway, New Jersey, USA, 1960.
- D. Nicholls, Complexes and First-Row Transition Elements, Macmillan Press, London, 1973.
- A. F. Wells, 'Structural Inorganic Chemistry, 5th ed., Oxford University Press, Oxford, UK, 1984.
- J. March, Advanced Organic Chemistry, 4th ed., p. 723, Wiley, New York, 1992.
- B. S. Furnell et al., Vogel's Textbook of Practical Organic Chemistry, 5th edition, Longman/Wiley, New York, 1989.
- Handbook of Reagents for Organic Synthesis: Acidic and Basic Reagents, (H. J. Reich, J. H. Rigby, eds.), Wiley, New York, 1999.
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