Titanium tetrabromide

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Titanium tetrabromide
Titanium tetrabromide
Ball-and-stick model of the titanium tetrabromide molecule
Names
IUPAC name
Titanium tetrabromide
Other names
Titanium(IV) bromide
Identifiers
7789-68-6 YesY
EC Number 232-185-0
Jmol 3D model Interactive image
PubChem 123263
  • InChI=1S/4BrH.Ti/h4*1H;/q;;;;+4/p-4
  • [Ti](Br)(Br)(Br)Br
Properties
TiBr4
Molar mass 367.483 g/mol
Appearance brown crystals
hygroscopic
Density 3.25 g/cm3
Melting point 39 °C (102 °F; 312 K)
Boiling point 230 °C (446 °F; 503 K)
decomposition
Solubility in other solvents chlorocarbons, benzene
Structure
cubic, Pa3, Z = 8
Tetrahedral
0 D
Vapor pressure {{{value}}}
Related compounds
Other anions
TiCl4
TiI4
Other cations
VCl4
Related compounds
TiCl3
VBr3
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Titanium tetrabromide is the chemical compound with the formula TiBr4. It is the most volatile transition metal bromide. The properties of TiBr4 are an average of TiCl4 and TiI4. Some key properties of these four-coordinated Ti(IV) species are their high Lewis acidity and their high solubility in nonpolar organic solvents. TiBr4 is diamagnetic, reflecting the d0 configuration of the metal centre.[1]

Preparation and structure

This four-coordinated complex adopts a tetrahedral geometry. It can be prepared via several methods: (i) from the elements, (ii) via the reaction of TiO2 with carbon and bromine (see Kroll process), and (iii) by treatment of TiCl4 with HBr.

Reactions

Titanium tetrabromide forms adducts such as TiBr4(THF)2 and [TiBr5].[2] With bulky donor ligands, such as 2-methylpyridine (2-Mepy), five-coordinated adducts form. TiBr4(2-MePy) is trigonal bipyramidal with the pyridine in the equatorial plane.[3]

TiBr4 has been used as a Lewis-acid catalyst in organic synthesis.[4]

The tetrabromide and tetrachlorides of titanium react to give a statistical mixture of the mixed tetrahalides, TiBr4-xClx (x = 0-4). The mechanism of this redistribution reaction is uncertain. One proposed pathway invokes the intermediacy of dimers.[5]

Safety

TiBr4 hydrolyzes rapidly, potentially dangerously, to release hydrogen bromide.

References

  1. Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
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