Molybdenum(III) chloride

(Redirected from Molybdenum trichloride)

Molybdenum(III) chloride is the inorganic compound with the formula MoCl3. It forms purple crystals.[1]

Molybdenum(III) chloride
Molybdenum(III) chloride alpha polymorph
Molybdenum(III) chloride alpha polymorph
α-MoCl3
Molybdenum(III) chloride beta polymorph
Molybdenum(III) chloride beta polymorph
β-MoCl3
Names
IUPAC names
Molybdenum(III) chloride
Molybdenum trichloride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.033.418 Edit this at Wikidata
EC Number
  • 236-775-9
UNII
  • InChI=1S/3ClH.Mo/h3*1H;/q;;;+3/p-3
    Key: ZSSVQAGPXAAOPV-UHFFFAOYSA-K
  • InChI=1/3ClH.Mo/h3*1H;/q;;;+3/p-3
    Key: ZSSVQAGPXAAOPV-DFZHHIFOAN
  • Cl[Mo](Cl)Cl
Properties
MoCl3
Molar mass202.30 g/mol
Appearancedark red solid
paramagnetic
Density3.58 g/cm3
Melting point410 °C (770 °F; 683 K) (decomposes)
insoluble
Solubilityinsoluble in ethanol, diethyl ether
+43.0·10−6 cm3/mol
Hazards
Flash pointNon-flammable
Related compounds
Other anions
Molybdenum(III) fluoride
Molybdenum(III) bromide
Molybdenum(III) iodide
Other cations
Chromium(IV) chloride
Tungsten(V) chloride
Related molybdenum chlorides
Molybdenum(II) chloride
Molybdenum(IV) chloride
Molybdenum(V) chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Synthesis and structure

Molybdenum(III) chloride is synthesized by the reduction of molybdenum(V) chloride with hydrogen.[2] A higher yield is produced by the reduction of pure molybdenum(V) chloride with anhydrous tin(II) chloride as the reducing agent.[3]

Molybdenum trichloride exists as two polymorphs: alpha (α) and beta (β). The alpha structure is similar to that of aluminum chloride (AlCl3). In this structure, molybdenum has octahedral coordination geometry and exhibits cubic close-packing in its crystalline structure. The beta structure, however, exhibits hexagonal close packing.[4]

Ether complexes

Molybdenum trichloride gives a ether complexes MoCl3(thf)3 and MoCl3(Et2O)3. They are beige, paramagnetic solids. Both feature octahedral Mo centers. The diethyl ether complex is synthesized by reducing a Et2O solution of MoCl5 with tin powder.[5] Older procedures involve stepwise reduction involving isolation of the Mo(IV)-thf complex.[6]

Hexa(tert-butoxy)dimolybdenum(III) is prepared by the salt metathesis reaction from MoCl3(thf)3:[7]

2 MoCl3(thf)3 + 6 LiOBu-t → Mo2(OBu-t)6 + 6 LiCl + 6 thf

References