Diboron tetrachloride
Names | |
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Preferred IUPAC name
Diboron tetrachloride | |
Systematic IUPAC name
Tetrachlorodiborane | |
Identifiers | |
13701-67-2 | |
3D model (Jmol) | Interactive image |
ChemSpider | 123068 |
PubChem | 139548 |
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Properties | |
B2Cl4 | |
Molar mass | 163.433 g/mol |
Appearance | colorless liquid |
Density | 1.5 g/cm3 (0 °C) |
Melting point | −92.6 °C (−134.7 °F; 180.6 K) |
Boiling point | 65.5 °C (149.9 °F; 338.6 K) |
Thermochemistry | |
137.7 J/mol K | |
Std molar entropy (S |
232.3 J/mol K |
Std enthalpy of formation (ΔfH |
-523 kJ/mol |
Gibbs free energy (ΔfG˚) |
-468.8 kJ/mol |
Related compounds | |
Related compounds |
Diboron tetrafluoride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Diboron tetrachloride is a chemical compound with the formula B2Cl4. It can be formed by the electrical discharge procedure of boron trichloride at low temperatures.[1]
Synthesis
The electrical discharge procedure of boron trichloride can be divided into three steps:[2]
- BCl3 → BCl2 + Cl
- Cl + Hg(electrode) → HgCl or HgCl2
- 2BCl2 → B2Cl4
Reactions
The compound is used as a reagent for the synthesis of organoboron compounds. For instance, diboron tetrachloride reacts with ethylene:[3]
- CH2=CH2 + B2Cl4 → Cl2BCH2CH2BCl2
The compound absorbs hydrogen quickly at room temperature:[2]
- 3 B2Cl4 + 6H2 → 2 B2H6 + 4 BCl3
References
- ↑ P. L. Timms (1972). Low Temperature Condensation. Advances in Inorganic Chemistry and Radiochemistry. p. 143. ISBN 0-12-023614-1.
- 1 2 Urry, Grant; Wartik, Thomas; Moore, R. E.; Schlesinger, H. I. (1954). "The Preparation and Some of the Properties of Diboron Tetrachloride, B2Cl41". Journal of the American Chemical Society. 76 (21): 5293–5298. doi:10.1021/ja01650a010. ISSN 0002-7863.
- ↑ Urry, Grant; Kerrigan, James; Parsons, Theran D.; Schlesinger, H. I. (1954). "Diboron Tetrachloride, B2Cl4, as a Reagent for the Synthesis of Organo-boron Compounds. I. The Reaction of Diboron Tetrachloride with Ethylene1". Journal of the American Chemical Society. 76 (21): 5299–5301. doi:10.1021/ja01650a011. ISSN 0002-7863.
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