Tungsten hexacarbonyl
Tungsten hexacarbonyl is an organometallic compound with the formula W6. This complex gave rise to the first example of a dihydrogen complex.
Like its chromium and molybdenum analogs, this colorless compound is noteworthy as a volatile, air-stable derivative of tungsten in its zero oxidation state.
Preparation, properties, and structure
Like many metal carbonyls, W6 is generally prepared by "reductive carbonylation", which involves the reduction of a metal halide with under an atmosphere of carbon monoxide. As described in a 2023 survey of methods "most cost-effective routes for the synthesis of group 6 hexacarbonyls are based on the reduction of the metal chlorides with magnesium, zinc or aluminium powders... under CO pressures".Another means of preparation involves heating iron pentacarbonyl and WCl6, resulting in the formation of ferrous chloride. The compound is relatively air-stable. It is sparingly soluble in nonpolar organic solvents. Tungsten carbonyl is widely used in electron beam-induced deposition technique - it is easily vaporized and decomposed by the electron beam providing a convenient source of tungsten atoms.W6 adopts an octahedral geometry consisting of six rod-like CO ligands radiating from the central W atom with dipole moment 0 debye.
Reactivity
All reactions of W6 commence with displacement of some CO ligands in W6. W6 behaves similarly to the Mo6 but tends to form compounds that are kinetically more robust. image:CP2W26.svg|thumb|left|144px|Cyclopentadienyltungsten tricarbonyl dimer 2W2 is produced from W6.Treatment of tungsten hexacarbonyl with sodium cyclopentadienide followed by oxidation of the resulting NaW3 gives cyclopentadienyltungsten tricarbonyl dimer.
One derivative is the dihydrogen complex W32.
Three of these CO ligands can be displaced by acetonitrile.
W6 has been used to desulfurize organosulfur compounds and as a precursor to catalysts for alkene metathesis.