Boron trichloride
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| Names | |||
|---|---|---|---|
| IUPAC name
Boron trichloride | |||
| Other names
Boron(III) chloride | |||
| Identifiers | |||
10294-34-5  | |||
| ChemSpider | 16788234 | ||
| EC number | 233-658-4 | ||
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| Jmol-3D images | Image | ||
| PubChem | 25135 | ||
| RTECS number | ED1925000 | ||
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| Properties | |||
| BCl3 | |||
| Molar mass | 117.17 g/mol | ||
| Appearance | Colorless gas, fumes in air | ||
| Density | 1.326 g/cm3 | ||
| Melting point | −107.3 °C (−161.1 °F; 165.8 K) | ||
| Boiling point | 12.6 °C (54.7 °F; 285.8 K)[1] | ||
| decomposes | |||
| Solubility | soluble in CCl4, ethanol | ||
| Refractive index (nD) |
1.00139 | ||
| Structure | |||
| Molecular shape | Trigonal planar (D3h) | ||
| Dipole moment | zero | ||
| Thermochemistry | |||
| Specific heat capacity (C) |
107 J/mol K | ||
| Std molar entropy (S |
206 J/mol K | ||
| Std enthalpy of formation (ΔfH |
-427 kJ/mol | ||
| Gibbs free energy (ΔfG˚) |
-387.2 kJ/mol | ||
| Hazards[2] | |||
| MSDS | ICSC | ||
| Main hazards | May be fatal if swallowed or if inhaled Causes serious burns to eyes, skin, mouth, lungs, etc. Contact with water gives HCl | ||
| GHS pictograms |    | ||
| GHS signal word | DANGER | ||
| H330, H300, H314[note 1] | |||
| EU Index | 005-002-00-5 | ||
| EU classification |  T+ (T+) C (C) | ||
| R-phrases | R14, R26/28, R34 | ||
| S-phrases | (S1/2), S9, S26, S28, S36/37/39, S45 | ||
| NFPA 704 | |||
| Flash point | Non-flammable | ||
| Related compounds | |||
| Other anions |
Boron trifluoride Boron tribromide Boron triiodide | ||
| Other cations |
Aluminium chloride Gallium chloride | ||
| Related compounds |
Boron trioxide Carbon tetrachloride | ||
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |||
verify (what is: / ?) | |||
| Infobox references | |||
Boron trichloride is the inorganic compound with the formula BCl3. This colorless gas is a valuable reagent in organic synthesis. It is highly reactive toward water.
Production and structure
Boron reacts with halogens to give the corresponding trihalides. Boron trichloride is, however, produced industrially by direct chlorination of boron oxide and carbon at 500 °C.
- B2O3 + 3 C + 3 Cl2 → 2 BCl3 + 3 CO
The carbothermic reaction is analogous to the Kroll process for the conversion of titanium dioxide to titanium tetrachloride. In the laboratory BF3 reacted with AlCl3 gives BCl3 via halogen exchange.[3] BCl3 is a trigonal planar molecule like the other boron trihalides, and has a bond length of 175pm.
A degree of π-bonding has been proposed to explain the short B− Cl distance although there is some debate as to its extent.[3] It does not dimerize, although NMR studies of mixtures of boron trihalides shows the presence of mixed halides. The absence of dimerisation contrasts with the tendencies of AlCl3 and GaCl3, which form dimers or polymers with 4 or 6 coordinate metal centres.
Reactions
BCl3 hydrolyzes readily to give hydrochloric acid and boric acid:
- BCl3 + 3 H2O → B(OH)3 + 3 HCl
Alcohols behave analogously giving the borate esters, e.g. trimethyl borate.
As a strong Lewis acid, BCl3 i forms adducts with tertiary amines, phosphines, ethers, thioethers, and halide ions.[4] Adduct formation is often accompanied by an increase in B-Cl bond length. BCl3 · S(CH3)2 (CAS# 5523-19-3) is often employed as a conveniently handled source of BCl3 because this solid (m.p. 88-90 °C) releases BCl3:
- (CH3)2S·BCl3 ⇌ (CH3)2S + BCl3
The mixed aryl and alkyl boron chlorides are also of known. Phenylboron dichloride is commercially available. Such species can be prepared by the redistribution reaction of BCl3 with organotin reagents:
- 2 BCl3 + R4Sn → 2 RBCl2 + R2SnCl2
Reduction
Reduction of BCl3 to elemental boron is conducted commercially (see below). In the laboratory, when boron trichloride can be converted to diboron tetrachloride by heating with copper metal:[5]
- 2 BCl3 + 2 Cu → B2Cl4 + CuCl
B4Cl4 can also be prepared in this way. Colourless diboron tetrachloride (m.p. -93 °C) is a planar molecule in the solid, (similar to dinitrogen tetroxide, but in the gas phase the structure is staggered.[3] It decomposes at room temperatures to give a series of monochlorides having the general formula (BCl)n, in which n may be 8, 9, 10, or 11. The compounds with formulas B8Cl8 and B9Cl9 are known to contain closed cages of boron atoms.
Uses
Boron trichloride is a starting material for the production of elemental boron. It is also used in the refining of aluminium, magnesium, zinc, and copper alloys to remove nitrides, carbides, and oxides from molten metal. It has been used as a soldering flux for alloys of aluminium, iron, zinc, tungsten, and monel. Aluminum castings can be improved by treating the melt with boron trichloride vapors. In the manufacture of electrical resistors, a uniform and lasting adhesive carbon film can be put over a ceramic base using BCl3. It has been used in the field of high energy fuels and rocket propellants as a source of boron to raise BTU value. BCl3 is also used in plasma etching in semiconductor manufacturing. This gas etches metal oxides by formation of a volatile BOClx compounds.
BCl3 is used as a reagent in the synthesis of organic compounds. Like the corresponding bromide, it cleaves C-O bonds in ethers.[1]
Safety
BCl3 is an aggressive reagent that can form hydrogen chloride upon exposure to moisture or alcohols. The dimethyl sulfide adduct (BCl3SMe2), which is a solid, is much safer to use,[6] when possible, but H2O will destroy the BCl3 portion while leaving dimethyl sulfide in solution.
See also
References
- ↑ 1.0 1.1 Yamamoto, Y.; Miyaura, N. (2004). "Boron Trichloride". In Paquette, L. Encyclopedia of Reagents for Organic Synthesis. New York: J. Wiley & Sons. doi:10.1002/047084289X.rb245.pub2. ISBN 0471936235.
- ↑ Index no. 005-002-00-5 of Annex VI, Part 3, to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006. OJEU L353, 31.12.2008, pp 1–1355 at p 341.
- ↑ 3.0 3.1 3.2 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0080379419.
- ↑ Gerrard, W., Lappert, M. F. (1958). "Reactions Of Boron Trichloride With Organic Compounds". Chemical Reviews 58 (6): 1081–1111. doi:10.1021/cr50024a003.
- ↑ Wartik, T.; Rosenberg, R.; Fox, W. B.; (1967). "Diboron Tetrachloride". Inorganic Syntheses 10. pp. 118–125. doi:10.1002/9780470132418.ch18.
- ↑ Williard, Paul G.; Fryhle, Craig B. (1980). "Boron trihalide-methyl sulfide complexes as convenient reagents for dealkylation of aryl ethers". Tetrahedron Letters 21 (39): 3731. doi:10.1016/0040-4039(80)80164-X.
Notes
- ↑ Within the European Union, the following additional hazard statement (EUH014) must also be displayed on labelling: Reacts violently with water.
Further reading
- Martin, D. R. (1944). "Coordination Compounds of Boron Trichloride. I. - A Review". Chemical Reviews 34 (3): 461–473. doi:10.1021/cr60109a005.
- Kabalka, G. W.; Wu, Z. Z.; Ju, Y. H. (2003). "The Use of Organoboron Chlorides and Bromides in Organic Synthesis". Journal of Organometallic Chemistry 680 (1–2): 12–22. doi:10.1016/S0022-328X(03)00209-2.
External links
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