Chromium(III) chloride (also called chromic chloride) is a violet coloured solid with the formula CrCl3.
Although it is ionic, the solid state structure is kinetically inert so that anhydrous CrCl3 is surprisingly reluctant to dissolve in water. However, in the presence of a trace of a reducing agent capable of reducing Cr3+ to Cr2+, the CrCl3 dissolves rapidly to form soluble complexes containing hydrated Cr3+ ions. The common commercial form of the hydrate is the dark green complex shown in the picture, [CrCl2(H2O)4]Cl.2H2O, but two other forms are known, viz., pale green [CrCl(H2O)5]Cl2.H2O and violet [Cr(H2O)6]Cl3.
This inertness means that CrCl3 is generally sluggish to react without the presence of a reducing agent. When it does react it undergoes ligand substitution reactions to form other complexes of chromium(III). It reacts as a Lewis acid, forming stable chloro complexes such as [CrCl6]3-.
The most common form of CrCl3 sold commercially is a dark green hexahydrate with the structure [CrCl2(H2O)4]Cl.2H2O, and like the anhydrous form it is also very inert towards substitution.
If substitution reactions are performed in the presence of a trace of Cr2+, then CrCl3 can undergo substitution with ligands such as water (giving violet [Cr(H2O)6]3+) or pyridine:
CrCl3 + 3 C5H5N → [CrCl3(C5H5N)3]
Such complexes are usually octahedral.
With molten alkali metal chlorides such as potassium chloride, CrCl3 gives octahedral complexes of the type K3CrCl6, as well as K3Cr2Cl9 which is also octahedral but where the two chromiums are linked via three chloride bridges.
Cr2O3(s) + 3 C(s) + 3 Cl2(g) → 2 CrCl3(s) + 3 CO(g)
It may also be prepared from the hexahydrate, by heating with thionyl chloride which reacts with the water of hydration.
The hydrated chlorides may be made by dissolving the metal in hydrochloric acid.
A significant use of CrCl3 in organic synthesis is for the in situ preparation of chromium(II) chloride, a popular reagent for (A) reduction of alkyl halides and for (B) the synthesis of (E)-alkenyl halides. The reaction is usually performed using two moles of CrCl3 per mole of lithium aluminium hydride, although if aqueous acidic conditions are appropriate zinc and hydrochloric acid may be sufficient.
Chromium(III) chloride has also been used as a Lewis acid in organic reactions, for example to catalyse the nitroso Diels-Alder reaction.