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Vanadium(III) bromide

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Vanadium(III) bromide
Vanadium(III) bromide
Vanadium(III) bromide
Names
IUPAC name
Vanadium(III) bromide
Other names
Vanadium tribromide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.033.382Edit this at Wikidata
EC Number
  • 236-736-6
RTECS number
  • YW2750000
  • InChI=1S/3BrH.V/h3*1H;/q;;;+3/p-3 checkY
    Key: ZOYIPGHJSALYPY-UHFFFAOYSA-K checkY
  • InChI=1/3BrH.V/h3*1H;/q;;;+3/p-3
    Key: ZOYIPGHJSALYPY-DFZHHIFOAP
  • Br[V](Br)Br
Properties
VBr3
Molar mass290.654 g/mol
AppearanceGreen-black solid
Density4 g/cm3
soluble
Solubilitysoluble in THF
(forms adduct)
+2890.0·10−6 cm3/mol
Structure
octahedral
Hazards
GHS labelling:[1]
GHS05: Corrosive
Danger
H314
P260,P264,P280,P301+P330+P331,P302+P361+P354,P304+P340,P305+P354+P338,P316,P321,P363,P405,P501
Related compounds
Otheranions
Vanadium(III) chloride
Othercations
Titanium(III) bromide
Molybdenum(III) bromide
Related compounds
Vanadium(II) bromide
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

Vanadium(III) bromide, also known as vanadium tribromide, describes theinorganic compounds with the formula VBr3 and its hydrates. The anhydrous material is a green-black solid. In terms of its structure, the compound ispolymeric with octahedral vanadium(III) surrounded by six bromide ligands.

Preparation

[edit]

VBr3 has been prepared by treatment ofvanadium tetrachloride withhydrogen bromide:

2 VCl4 + 8 HBr → 2 VBr3 + 8 HCl + Br2

The reaction proceeds via the unstable vanadium(IV) bromide (VBr4), which releases Br2 near room temperature.[2]

It is also possible to prepare vanadium(III) bromide by reactingbromine with vanadium or ferrovanadine:[3]

2 V + 3 Br2 → 2 VBr3
2 VFe + 6 Br2 → 2 VBr3 + FeBr3

Properties

[edit]

Physical

[edit]

Vanadium(III) bromide is present in the form of black, leafy, very hygroscopic crystals with a sometimes greenish sheen. It is soluble in water with green color. Its crystal structure is isotypic to that ofvanadium(III) chloride withspace group R3c (space group no. 167),a = 6.400 Å,c = 18.53 Å. When heated to temperatures of around 500 °C, a violet gas phase is formed, from which, under suitable conditions, red vanadium(IV) bromide can be separated by rapid cooling, which decomposes at −23 °C.[3]

Chemical

[edit]

Likevanadium(III) chloride, vanadium(III) bromide forms red-brown soluble complexes with dimethoxyethane andTHF, such asmer-VBr3(THF)3.[4]

Aqueous solutions prepared from VBr3 contain the cationtrans-[VBr2(H2O)4]+. Evaporation of these solutions give the salt trans-[VBr2(H2O)4]Br.(H2O)2.[5]

Further reading

[edit]
  • Stebler, A.; Leuenberger, B.; Guedel, H. U. "Synthesis and crystal growth of A3M2X9 (A = Cs, Rb; M = Ti, V, Cr; X = Cl, Br)" Inorganic Syntheses (1989), volume 26, pages 377–85.

References

[edit]
  1. ^PubChem."Vanadium(iii) bromide".pubchem.ncbi.nlm.nih.gov. Retrieved2026-02-03.
  2. ^Calderazzo, Fausto; Maichle-Mössmer, Cäcilie; Pampaloni, Guido; Strähle, Joachim (1993). "Low-Temperature Syntheses of Vanadium(III) and Molybdenum(IV) Bromides by Halide Exchange".J. Chem. Soc., Dalton Trans. (5):655–658.doi:10.1039/DT9930000655.
  3. ^abBrauer, Georg (1975).Handbuch der präparativen anorganischen Chemie Volume 3 (in German). the University of Michigan: Enke. p. 1409.ISBN 978-3-432-87823-2.
  4. ^G. W. A. Fowles, G. W. A.; Greene, P. T.; Lester, T. E. "Ether Complexes of Tervalent Titanium and Vanadium" J. Inorg, Nucl. Chem., 1967. Vol. 29. pp. 2365 to 2370.
  5. ^Donovan, William F.; Smith, Peter W. (1975). "Crystal and Molecular Structures of Aquahalogenovanadium(III) Complexes. Part I. X-Ray Crystal Structure oftrans-Tetrakisaquadibromo-Vanadium(III) Bromide Dihydrate and the Isomorphous Chloro- Compound".Journal of the Chemical Society, Dalton Transactions (10): 894.doi:10.1039/DT9750000894.
Vanadium(0)
Vanadium(II)
Vanadium(III)
Organovanadium(III) compounds
Vanadium(IV)
Organovanadium(IV) compounds
Vanadyl(IV) compounds
Oxovanadates(IV)
Vanadium(V)
Vanadyl(V) compounds
Oxovanadates(V)
Salts and covalent derivatives of thebromide ion
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