Disulfur diiodide

Disulfur diiodide

  Sulfur, S
  Iodine, I
Names
IUPAC name
Diiododisulfane
Other names
Sulfur monoiodide (incorrect name)
Identifiers
CAS Number
  • 53280-15-2 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 31043639
ECHA InfoCard 100.053.127 Edit this at Wikidata
EC Number
  • 258-458-4
PubChem CID
  • 71774781
CompTox Dashboard (EPA)
  • DTXSID101315384 Edit this at Wikidata
InChI
  • InChI=1S/I2S2/c1-3-4-2
    Key: NJLGSHIGTKGJLG-UHFFFAOYSA-N
  • S(SI)I
Properties
Chemical formula
S2I2
Molar mass 317.93 g·mol−1
Appearance Reddish-brown solid
Melting point −30 °C (−22 °F; 243 K) (decomposes)
Solubility Soluble in carbon tetrachloride, slightly soluble in pentane
Structure
Point group
C2
Coordination geometry
2 at sulfur atoms
Molecular shape
gauche
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Disulfur diiodide is an unstable inorganic chemical compound with the chemical formula S2I2. It is a red-brown solid that decomposes above −30 °C to elemental sulfur and iodine.[1]

Production

Reaction of sulfur and iodine

The first attempt and claim to produce a sulfur iodide were made in 1813 by Bernard Courtois when exploring the properties of his newly discovered element, iodine. He reacted to sulfur and iodine, claiming they had made a compound. However, this production was doubted by Gay-Lussac. Between 1827 and 1896, more attempts were made to make sulfur iodide by combining the elements; however, all were inconclusive on the existence of the compound or failed. Later, when thermal analysis was developed, it was shown that when the elements were combined, it only resulted in a mixture, not a compound.[2]

Production by double replacement

When attempts to produce sulfur iodide by the direct combination of the elements failed to overcome the low thermodynamic stability of the compound, production by double replacement was attempted between 1833 and 1886. Some reactions that were attempted was the reaction of disulfur dichloride and hydroiodic acid:[2]

S2Cl2 + 2 HI → S2I2 + 2 HCl

The reaction of hydrogen sulfide and iodine trichloride:

3 H2S + 2 ICl3 → S3I2 + 6 HCl

The reaction of hydroiodic acid and sulfur:

2 HI + 3 S → H2S + S2I2

The reaction of disulfur dichloride and potassium iodide:

S2Cl2 + 2 KI → S2I2 + 2 KCl

and more, all assumed to have failed to produce sulfur iodide. However, the reaction between S2Cl2 and HI attempted in 1835 was later proven to have produced disulfur diiodide.[2]

In 1940, another production was attempted with the fourth reaction and was reported to have detected various sulfur iodides, such as disulfur diiodide and sulfur diiodide (SI2). When observing the reaction of very dilute disulfur dichloride in carbon tetrachloride and potassium iodide:[2][3]

S2Cl2 + 2 KI → 2 S + I2 + 2 KCl

they observed a color change from yellow to reddish-brown to finally violet, which was assumed to be evidence for the formation of sulfur iodides. The compound was found to decompose at room temperature slowly in a solution, with the decomposition rate increasing with increasing temperature.[3]

Isolation

Disulfur diiodide was first isolated by the reaction of disulfur dichloride and potassium iodide, sodium iodide, or hydrogen iodide in pentane at −90 °C, and verified by infrared spectroscopy.[4][5]

Properties

Disulfur diiodide is light-sensitive and is soluble in various haloalkanes, such as carbon tetrachloride.[3]

Other sulfur iodides

Sulfur diiodide (SI2) has finally been reported in an argon matrix at 9 K by the reaction of sulfur dichloride and iodine; however, this has been disputed.[6]

Sulfur and iodine react in antimony pentafluoride or arsenic pentafluoride to form the S7I+ ion, which is stable at room temperature, unlike other sulfur-iodine compounds.[7]

The empirical formula of disulfur diiodide is SI. It is therefore sometimes called sulfur monoiodide, but S2I2 is a covalently bound molecule and is not the same as a SI molecule or an ionic salt having 1:1 stoichiometry. The true sulfur monoiodide molecule is a radical.[8]

References

  1. ^ Wiberg, Egon; Nils Wiberg; Arnold Frederick Holleman (2001). Inorganic chemistry. Academic Press. p. 529. ISBN 978-0-12-352651-9.
  2. ^ a b c d William B. Jensen (2016). The Search for Sulfur Iodide : Notes from the Oesper Collections, No. 37. University of Cincinnati. Archived from the original on 2022-12-25. Retrieved 2022-12-23.
  3. ^ a b c M. R. Aswathanarayana Rao (1940). "Investigations on the Iodides of Sulphur". Proceedings of the Indian Academy of Sciences. 11 (3): 162–174.
  4. ^ Gisela Vahl; Priv.-Doz. Dr. Rolf Minkwitz (1978). "Beiträge zur Chemie der Schwefelhalogenide. IV. Über Versuche zur Darstellung von festem Dijoddisulfan bei tiefen Temperaturen" [Contributions of the Chemistry of Sulfur Halides. IV. On the Preparation of Solid Disulfurdiiodide at Low Temperatures]. Zeitschrift für anorganische und allgemeine Chemie (in German). 443 (1). Wiley: 217–224. doi:10.1002/zaac.19784430124.
  5. ^ Gisela Krummel; Rolf Minkwitz (1977). "Infrared-spectroscopic investigations on solid disulfurdiiodine". Inorganic and Nuclear Chemistry Letters. 13 (5): 213–215. doi:10.1016/0020-1650(77)80096-2.
  6. ^ Martin Feuerhahn; Gisela Vahl (1980). "Infrared spectra of matrix isolated sulfur dibromide and sulfur diiodide". Inorganic and Nuclear Chemistry Letters. 16 (1): 5-8. doi:10.1016/0020-1650(80)80082-1.
  7. ^ T. Klapoetke; J. Passmore (1989). "Sulfur and selenium iodine compounds: from non-existence to significance". Accounts of Chemical Research. 22 (7). ACS Publications: 234–240. doi:10.1021/ar00163a002.
  8. ^ See SciFinder CAS No 1312-15-8 for main refs
  • v
  • t
  • e
Sulfides and
disulfides
  • Al2S3
  • As2S2
  • As2S3
  • As2S5
  • As4S4
  • Au2S
  • Au2S3
  • B2S3
  • BaS
  • BeS
  • Bi2S3
  • CS2
  • C3S2
  • C6S6
  • CaS
  • CdS
  • CeS
  • CoS
  • Cr2S3
  • CSSe
  • CSTe
  • CuFeS2
  • CuS
  • D2S
  • Dy2S3
  • Er2S3
  • EuS
  • FeS2
  • GaS
  • H2S
  • HfS2
  • HgS
  • In2S3
  • K2S
  • LaS
  • LiS
  • MgS
  • MoS2
  • MoS3
  • NaHS
  • Na2S
  • NH4HS
  • NiS
  • P4Sx
  • PbS
  • PbS2
  • PSCl3
  • PSI3
  • PtS
  • ReS2
  • Re2S7
  • SiS
  • SrS
  • TlS
  • VS
  • SeS2
  • S2U
  • WS2
  • WS3
  • Sb2S3
  • Sb2S5
  • Sb4S3O3
  • Sm2S3
  • Y2S3
  • ZrS2
  • La
    2
    O
    2
    S
  • Gd
    2
    O
    2
    S
Sulfur halides
  • S2Br2
  • SBr2
  • S2Cl2
  • SCl2
  • SCl4
  • SF2
  • SF4
  • S2F10
  • SF6
  • S2I2
Sulfur oxides
and oxyhalides
  • SO2
  • SO3
  • SOBr2
  • SOCl2
  • SOF2
  • SOF4
  • H2S3O6
  • H2SO3
  • H2SO4
  • H2S2O7
  • H2SO5
Sulfites
  • CdSO3
  • K2SO3
Sulfates
  • Ag2SO4
  • CaSO4
  • CuSO4
  • Cs2SO4
  • Er2(SO4)3
  • Eu2(SO4)3
  • HgSO4
  • K2SO4
  • KAl(SO4)2
  • NaAl(SO4)2
  • RaSO4
  • SnSO4
  • SrSO4
  • Ti(SO4)2
  • Tm2(SO4)3
  • Yb2(SO4)3
  • Zr(SO4)2
Thiocyanates
Organic compounds
  • C2H4S
  • C2H6S3
  • C4H4S
  • C32H66S2
  • CHCl3S
  • C2H3SN
  • v
  • t
  • e
Salts and covalent derivatives of the iodide ion
HI
+H
He
LiI BeI2 BI3
+BO3
CI4
+C
NI3
NH4I
+N
I2O4
I2O5
I4O9
IF
IF3
IF5
IF7
Ne
NaI MgI2 AlI
AlI3
SiI4 PI3
P2I4
+P
PI5
S2I2 ICl
ICl3
Ar
KI CaI2 ScI3 TiI2
TiI3
TiI4
VI2
VI3
CrI2
CrI3
MnI2 FeI2
FeI3
CoI2 NiI2
-Ni
CuI ZnI2 GaI
GaI3
GeI2
GeI4
+Ge
AsI3
As2I4
+As
Se IBr
IBr3
Kr
RbI
RbI3
SrI2 YI3 ZrI2
ZrI3
ZrI4
NbI4
NbI5
MoI2
MoI3
TcI3 RuI3 RhI3 PdI2 AgI CdI2 InI
InI3
SnI2
SnI4
SbI3
+Sb
TeI4
+Te
I
I
3
Xe
CsI
CsI3
BaI2   LuI3 HfI3
HfI4
TaI4
TaI5
WI2
WI3
WI4
ReI3
ReI
4
OsI
OsI2
OsI3
IrI3
IrI
4
PtI2
PtI4
AuI
AuI3
Hg2I2
HgI2
TlI
TlI3
PbI2 BiI3 PoI2
PoI4
AtI Rn
Fr RaI2   Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
LaI2
LaI3
CeI2
CeI3
PrI2
PrI3
NdI2
NdI3
PmI3 SmI2
SmI3
EuI2
EuI3
GdI2
GdI3
TbI3 DyI2
DyI
3
HoI3 ErI3 TmI2
TmI3
YbI2
YbI3
AcI3 ThI2
ThI3
ThI4
PaI4
PaI5
UI3
UI4
NpI3 PuI3 AmI2
AmI3
CmI3 BkI
3
CfI
2

CfI
3
EsI2
EsI3
Fm Md No