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![]() Sulfur, S; Bromine, Br | |
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Names | |
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IUPAC names Disulfur dibromide Dibromodisulfane | |
Systematic IUPAC name Bromosulfanyl thiohypobromite | |
Identifiers | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.032.821 |
EC Number |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
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Properties | |
S2Br2 | |
Molar mass | 223.93 g·mol−1 |
Appearance | Orange/yellow liquid |
Density | 2.703 g/cm3 |
Melting point | −46 °C (−51 °F; 227 K) [1] |
Boiling point | 46–48 °C (115–118 °F; 319–321 K) (0.1 mmHg) |
hydrolyzes | |
Structure | |
C2 | |
2 at sulfur atoms | |
gauche | |
Thermochemistry | |
Std molar entropy (S⦵298) | 350.52 J/(mol·K) [2] |
Std enthalpy of formation (ΔfH⦵298) | 30.96 kJ/mol [2] |
Hazards | |
GHS labelling: | |
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Danger | |
Safety data sheet (SDS) | ICSC 1661 |
Related compounds | |
Related | |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Disulfur dibromide is the inorganic compound with the formula S 2 Br 2. It is a yellow-brown liquid that fumes in air. It is prepared by direct combination of the elements and purified by vacuum distillation. [3] Higher yields can be obtained from disulfur dichloride and 50% aqueous hydrobromic acid, but the product must be promptly removed from water, lest it hydrolyze. [1] The compound has no particular application,[ citation needed ] unlike the related sulfur compound disulfur dichloride, although acidic alcoholysis is "an excellent synthesis of alkyl bromides." [1]
The molecular structure is Br−S−S−Br, akin to that of disulfur dichloride (S2Cl2). According to electron diffraction measurements, the angle between the Bra−S−S and S−S−Brb planes is 84° and the Br−S−S angle is 107°. The S−S distance is 198.0 pm, circa 5.0 pm shorter than for S2Cl2. [4]