Vanadium(III) chloride


Vanadium trichloride is the inorganic compound with the formula VCl3. This purple salt is a common precursor to other vanadium complexes.

Structure

VCl3 has the common BiI3 structure, a motif that features hexagonally closest-packed chloride framework with vanadium ions occupying the octahedral holes. VBr3 and VI3 adopt the same structure, but VF3 features a structure more closely related to ReO3. VCl3 is paramagnetic and has two unpaired electrons.

Preparation and reactions

VCl3 is prepared by heating VCl4 at 160–170 °C under a flowing stream of inert gas, which sweeps out the Cl2. The bright red liquid converts to a purple solid.
Heating of VCl3 decomposes with volatilization of VCl4, leaving VCl2. Upon heating under H2 at 675 °C, VCl3 reduces to greenish VCl2.
Comproportionation of vanadium trichloride and vanadium oxides gives vanadium oxydichloride:
Vanadium trichloride catalyses the pinacol coupling reaction of benzaldehyde to 1,2-diphenyl-1,2-ethanediol by various reducing metals such as zinc:

Complexes

VCl3 forms colorful adducts and derivatives with a broad scale of ligands. VCl3 dissolves in water to give the hexahydrate, but the formula is deceptive. The salt is described by the formula Cl.2H2O. In other words, two of the water molecules are not bound to the vanadium, whose structure resembles the corresponding Fe derivative. Removal of the two bound chloride ligands from + in aqueous solution gives the green ion 3+.
With tetrahydrofuran, VCl3 forms the red/pink adduct VCl33. With acetonitrile, one obtains the green adduct VCl33.
When treated with KCN, VCl3 converts to 4−. It is common for early metals to adopt high coordination numbers with compact ligands. Complementarily, larger metals can form complexes with rather bulky ligands. This aspect is illustrated by the isolation of VCl32, containing two bulky NMe3 ligands.

Precursor to organometallics

The reactive species V3 forms from VCl3.
This species binds CO and, under appropriate conditions, N2.