Manganese(II) chloride

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Manganese(II) chloride
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Template:Longitem MnCl2
Molar mass 125.844 g/mol (anhydrous)
161.874 g/mol (dihydrate)
197.91 g/mol (tetrahydrate)
Appearance pink solid (tetrahydrate)
Density 2.977 g/cm3 (anhydrous)
2.27 g/cm3 (dihydrate)
2.01 g/cm3 (tetrahydrate)
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Solubility slightly soluble in pyridine, soluble in ethanol
insoluble in ether
Template:Longitem +14,350·10−6 cm3/mol
Template:Longitem CdCl2
Template:Longitem octahedral
Template:Longitem Manganese(II) fluoride
Manganese(II) bromide
Manganese(II) iodide
Template:Longitem Manganese(III) chloride
Technetium(IV) chloride
Rhenium(III) chloride
Rhenium(IV) chloride
Rhenium(V) chloride
Rhenium(VI) chloride
Template:Longitem Chromium(II) chloride
Iron(II) chloride

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Manganese(II) chloride is the dichloride salt of manganese, MnCl2. This inorganic chemical exists in the anhydrous form, as well as the dihydrate (MnCl2·2H2O) and tetrahydrate (MnCl2·4H2O), with the tetrahydrate being the most common form. Like many Mn(II) species, these salts are pink, with the paleness of the color being characteristic of transition metal complexes with high spin d5 configurations.[1]

Preparation

Manganese chloride is produced by treating manganese(IV) oxide with concentrated hydrochloric acid.

MnO2 + 4 HCl → MnCl2 + 2 H2O + Cl2

In the 19th century this reaction was used for the manufacture of chlorine. By carefully neutralizing the resulting solution with MnCO3, one can selectively precipitate iron salts, which are common impurities in manganese dioxide.[2] In the laboratory, manganese chloride can be prepared by treating manganese metal or manganese(II) carbonate with hydrochloric acid:

Mn + 2 HCl + 4 H2O → MnCl2(H2O)4 + H2
MnCO3 + 2 HCl + 3 H2O → MnCl2(H2O)4 + CO2

Structures

Anhydrous MnCl2 adopts a layered cadmium chloride-like structure. The tetrahydrate consists of octahedral cis-Mn(H2O)4Cl2 molecules. The trans isomer, which is metastable, is also known.[3][4] The dihydrate MnCl2(H2O)2 is a coordination polymer. Each Mn center is coordinated to four doubly bridging chloride ligands. The octahedron is completed by a pair of mutually trans aquo ligands.[5] Script error: No such module "Multiple image".

Chemical properties

The hydrates dissolve in water to give mildly acidic solutions with a pH of around 4. These solutions consist of the metal aquo complex [Mn(H2O)6]2+.

It is a weak Lewis acid, reacting with chloride ions to produce a series of salts containing the following ions [MnCl3], [MnCl4]2−, and [MnCl6]4−.

Upon treatment with typical organic ligands, manganese(II) undergoes oxidation by air to give Mn(III) complexes. Examples include [Mn(EDTA)], [Mn(CN)6]3−, and [Mn(acetylacetonate)3]. Triphenylphosphine forms a labile 2:1 adduct:

MnCl2 + 2 Ph3P → [MnCl2(Ph3P)2]

Anhydrous manganese(II) chloride serves as a starting point for the synthesis of a variety of organomanganese compounds. For example, manganocene is prepared by reaction of MnCl2 with a solution of sodium cyclopentadienide in tetrahydrofuran (THF).

MnCl2 + 2 NaC5H5 → Mn(C5H5)2 + 2 NaCl

Similar reactions are used in the preparation of the antiknock compound methylcyclopentadienyl manganese tricarbonyl.[2]

Manganese chloride is a precursor to organomanganese reagents in organic chemistry.[6][7]

Manganese chloride is mainly used in the production of dry cell batteries.

Magnetism

Manganese(II) salts are paramagnetic. As such the presence of such salts profoundly affect NMR spectra.[8]

Natural occurrence

Scacchite is the natural, anhydrous form of manganese(II) chloride.[9]

Precautions

Manganism, or manganese poisoning, can be caused by long-term exposure to manganese dust or fumes.

References

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  1. N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth-Heinemann, Oxford, UK, 1997.
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  4. A. F. Wells, Structural Inorganic Chemistry, 5th ed., Oxford University Press, Oxford, UK, 1984.
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External links

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