Disulfur dibromide
{{Chembox
| Watchedfields = changed
| verifiedrevid = 408467094
| Name = Disulfur dibromide
| ImageFile1 = Disulfur-dibromide-2D-dimensions.png
| ImageName1 = Ball-and-stick model of sulfur dibromide
| ImageFile2 = Disulfur-dibromide-3D-balls.png
| ImageName2 = Disulfur-dibromide-3D-vdW.png
| ImageCaption2 = {{color box|yellow}} Sulfur, S; {{color box|maroon}} Bromine, Br
| ImageFile3 = Sulphur bromide.jpg
| IUPACName = Disulfur dibromide
Dibromodisulfane
| OtherNames =
| SystematicName = Bromosulfanyl thiohypobromite
| Section1 = {{Chembox Identifiers
| CASNo = 13172-31-1
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = L9DU8F2SHZ
| ChemSpiderID = 109902
| PubChem = 123296
| RTECS =
| EINECS = 236-119-1
| UNNumber =
| SMILES = S(SBr)Br
| StdInChIKey = JIRDGEGGAWJQHQ-UHFFFAOYSA-N
| StdInChI = InChI=1S/Br2S2/c1-3-4-2
}}
| Section2 = {{Chembox Properties
| Formula = {{chem2|S2Br2}}
| S=2|Br=2
| Appearance = Orange/yellow liquid
| Density = 2.703 g/cm3
| Solubility = hydrolyzes
| MeltingPtC = -46
| BoilingPtC = 46-48
| BoilingPt_notes = (0.1 mmHg)
| RefractIndex =
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| Section3 = {{Chembox Structure
| Coordination = 2 at sulfur atoms
| MolShape = gauche
| PointGroup = C2
| Dipole =
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| Section4 = {{Chembox Thermochemistry
}}
| Section7 = {{Chembox Hazards
| ExternalSDS = [http://www.inchem.org/documents/icsc/icsc/eics1661.htm ICSC 1661]
| GHSPictograms = {{GHS05}}{{GHS07}}{{GHS09}}
| GHSSignalWord = Danger
| HPhrases = {{H-phrases|}}
| PPhrases = {{P-phrases|}}
| NFPA-H =
| NFPA-F =
| NFPA-R =
| NFPA-S =
| AutoignitionPt =
| PEL =
}}
| Section8 = {{Chembox Related
| OtherFunction = {{ubl|Sulfur dibromide|Thionyl bromide|Sulfuryl bromide}}
| OtherCompounds = {{ubl|Hydrogen disulfide|Disulfur difluoride|Disulfur dichloride|Disulfur diiodide}}
}}
}}
Disulfur dibromide is the inorganic compound with the formula {{chem2|S2Br2|auto=1}}. It is a yellow-brown liquid that fumes in air. It is prepared by direct combination of the elements and purified by vacuum distillation.{{cite book|author=F. Fehér|chapter=Dibromodisulfane|title=Handbook of Preparative Inorganic Chemistry, 2nd Ed.|editor=G. Brauer|publisher=Academic Press|year=1963|place=NY, NY|volume=1|pages=377–378}} 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.{{cite book|title=Sulfur in Organic and Inorganic Chemistry|volume=1|editor-first=Alexander|editor-last=Senning|year=1971|publisher=Marcel Dekker|location=New York|lccn=70-154612|isbn=0-8247-1615-9|first=Philip S.|last=Magee|chapter=The Sulfur–Bromine Bond|pages=264–267}} The compound has no particular application,{{cn|date=November 2024}} unlike the related sulfur compound disulfur dichloride, although acidic alcoholysis is "an excellent synthesis of alkyl bromides."
The molecular structure is {{chem2|Br\sS\sS\sBr}}, akin to that of disulfur dichloride ({{chem2|S2Cl2}}). According to electron diffraction measurements, the angle between the {{chem2|Br^{a}\sS\sS}} and {{chem2|S\sS\sBr^{b}|}} planes is 84° and the {{chem2|Br\sS\sS}} angle is 107°. The {{chem2|S\sS}} distance is 198.0 pm, circa 5.0 pm shorter than for {{chem2|S2Cl2}}.{{cite journal|title=Comparison of the Structural Properties of Compounds Containing the XSSX Moiety (X = H, Me, R, Cl, Br, F, OR)|last1=Zysman-Colman|first1=Eli|last2=Harpp|first2=David|journal=Journal of Sulfur Chemistry|year=2004|volume=25|issue=4 |page=291-316|doi=10.1080/17415990410001710163|s2cid=95468251}}
References
{{Sulfur compounds}}
{{Bromides}}
{{Bromine compounds}}