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Selenium tetrachloride

From Wikipedia, the free encyclopedia
Selenium tetrachloride
Names
IUPAC name
Selenium tetrachloride
Other names
Selenium(IV) chloride, tetrachloro-λ4-selane
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.030.036Edit this at Wikidata
EC Number
  • 233-053-5
RTECS number
  • VS7875000
UNII
  • InChI=1S/Cl4Se/c1-5(2,3)4 checkY
    Key: LNBXMNQCXXEHFT-UHFFFAOYSA-N checkY
  • InChI=1/Cl4Se/c1-5(2,3)4
    Key: LNBXMNQCXXEHFT-UHFFFAOYAD
  • Cl[Se](Cl)(Cl)Cl
Properties
SeCl4
Molar mass220.771 g/mol
Appearancewhite to yellow crystals
Density2.6 g/cm3, solid
Melting pointsublimes at 191.4 °C[1]
decomposes in water
Structure
Monoclinic,mS80
C12/c1, No. 15
Seesaw (gas phase)[citation needed]
Hazards[2]
GHS labelling:
GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
Danger
H301,H331,H373,H410
P260,P261,P264,P270,P271,P273,P301+P310,P304+P340,P311,P314,P321,P330,P391,P403+P233,P405,P501
NFPA 704 (fire diamond)
Flash pointnon-flammable
Related compounds
Otheranions
Selenium tetrafluoride
Selenium tetrabromide
Selenium dioxide
Othercations
Dichlorine monoxide
Sulfur tetrachloride
Tellurium tetrachloride
Related compounds
Selenium dichloride
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Selenium tetrachloride is theinorganic compound composed with theformula SeCl4. This compound exists as yellow to white volatile solid. It is one of two commonly availableselenium chlorides, the other example beingselenium monochloride, Se2Cl2. SeCl4 is used in the synthesis of otherselenium compounds.

Synthesis and structure

[edit]
Structure of selenium tetrachloride

The compound is prepared by treatingselenium withchlorine.[3] When the reacting selenium is heated, the productsublimes from the reaction flask. The volatility of selenium tetrachloride can be exploited to purification of selenium.

Solid SeCl4 is actually atetramericcubane-type cluster, for which the Se atom of an SeCl6 octahedron sits on four corners of the cube and the bridging Cl atoms sit on the other four corners. The bridging Se-Cl distances are longer than the terminal Se-Cl distances, but all Cl-Se-Cl angles are approximately 90°.[4]

SeCl4 has often been used as an example for teachingVSEPR rules ofhypervalent molecules. As such, one would predict four bonds but five electron groups giving rise to aseesaw geometry. This clearly is not the case in thecrystal structure. Others have suggested that the crystal structure can be represented as SeCl3+ and Cl. This formulation would predict apyramidal geometry for the SeCl3+ cation with a Cl-Se-Cl bond angle of approximately 109°. However, this molecule is an excellent example of a situation where maximal bonding cannot be achieved with the simplest molecular formula. The formation of the tetramer (SeCl4)4,[5] with delocalized sigma bonding of the bridging chloride is clearly preferred over a "hypervalent" small molecule.Gaseous SeCl4 contains SeCl2 and chlorine, which recombine upon condensation.

Reactions

[edit]

Selenium tetrachloride can be reduced in situ to the dichloride usingtriphenylstibine:

SeCl4 + SbPh3 → SeCl2 + Cl2SbPh3

Selenium tetrachloride reacts with water to giveselenous andhydrochloricacids:[6][page needed]

SeCl4 + 3 H2O → H2SeO3 + 4 HCl

Upon treatment withselenium dioxide, it givesselenium oxychloride:[6][page needed]

SeCl4 + SeO2 → 2SeOCl2

References

[edit]
  1. ^Lide, David R. (1998).Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. p. 487.ISBN 0-8493-0594-2. Retrieved2008-07-02.
  2. ^"323527 Selenium tetrachloride". Sigma-Aldrich. Retrieved2008-07-02.
  3. ^Nowak, H. G.; Suttle, J. F.; Parker, W. E.; Kleinberg, J. (1957). "Selenium (IV) Chloride".Inorganic Syntheses. Vol. 5. p. 125.doi:10.1002/9780470132364.ch33.ISBN 9780470132364.{{cite book}}:ISBN / Date incompatibility (help)
  4. ^Kristallstruktur der stabilen Modifikation von SeCl4, Zeitschrift für Naturforschung, 36b, 1660, 1981
  5. ^Wells,Structural Inorganic Chemistry, fifth ed, Oxford, p. 709,ISBN 0-19-855370-6
  6. ^abGreenwood, Norman N.; Earnshaw, Alan (1997).Chemistry of the Elements (2nd ed.).Butterworth-Heinemann.doi:10.1016/C2009-0-30414-6.ISBN 978-0-08-037941-8.
Selenium compounds
Se(−II)
Se(0,I)
Se(I)
Se(II)
Se(III)
Se(IV)
Se(VI)
Se(IV,VI)
Salts and covalent derivatives of thechloride ion
HClHe
LiClBeCl2B4Cl4
B12Cl12
BCl3
B2Cl4
+BO3
C2Cl2
C2Cl4
C2Cl6
CCl4
+C
+CO3
NCl3
ClN3
+N
+NO3
ClxOy
Cl2O
Cl2O2
ClO
ClO2
Cl2O4
Cl2O6
Cl2O7
ClO4
+O
ClF
ClF3
ClF5
Ne
NaClMgCl2AlCl
AlCl3
Si5Cl12
Si2Cl6
SiCl4
P2Cl4
PCl3
PCl5
+P
S2Cl2
SCl2
SCl4
+SO4
Cl2Ar
KClCaCl
CaCl2
ScCl3TiCl2
TiCl3
TiCl4
VCl2
VCl3
VCl4
VCl5
CrCl2
CrCl3
CrCl4
MnCl2
MnCl3
FeCl2
FeCl3
CoCl2
CoCl3
NiCl2CuCl
CuCl2
ZnCl2GaCl
GaCl3
GeCl2
GeCl4
AsCl3
AsCl5
+As
Se2Cl2
SeCl2
SeCl4
BrClKr
RbClSrCl2YCl3ZrCl2
ZrCl3
ZrCl4
NbCl3
NbCl4
NbCl5
MoCl2
MoCl3
MoCl4
MoCl5
MoCl6
TcCl3
TcCl4
RuCl2
RuCl3
RuCl4
RhCl3PdCl2AgClCdCl2InCl
InCl2
InCl3
SnCl2
SnCl4
SbCl3
SbCl5
Te3Cl2
TeCl2
TeCl4
ICl
ICl3
XeCl
XeCl2
XeCl4
CsClBaCl2*LuCl3
177LuCl3
HfCl4TaCl3
TaCl4
TaCl5
WCl2
WCl3
WCl4
WCl5
WCl6
ReCl3
ReCl4
ReCl5
ReCl6
OsCl2
OsCl3
OsCl4
OsCl5
IrCl2
IrCl3
IrCl4
PtCl2
PtCl4
PtCl2−6
AuCl
(Au[AuCl4])2
AuCl3
AuCl4
Hg2Cl2
HgCl2
TlCl
TlCl3
PbCl2
PbCl4
BiCl3PoCl2
PoCl4
AtClRn
FrClRaCl2**LrCl3RfCl4DbCl5SgO2Cl2BhO3ClHsMtDsRgCnNhFlMcLvTsOg
 
*LaCl3CeCl3PrCl3NdCl2
NdCl3
PmCl3SmCl2
SmCl3
EuCl2
EuCl3
GdCl3TbCl3DyCl2
DyCl3
HoCl3ErCl3TmCl2
TmCl3
YbCl2
YbCl3
**AcCl3ThCl3
ThCl4
PaCl4
PaCl5
UCl3
UCl4
UCl5
UCl6
NpCl3
NpCl4
PuCl3
PuCl4
PuCl2−6
AmCl2
AmCl3
CmCl3BkCl3CfCl3
CfCl2
EsCl2
EsCl3
FmCl2MdCl2NoCl2
Receptor
(ligands)
DP (D2)Tooltip Prostaglandin D2 receptor
DP1Tooltip Prostaglandin D2 receptor 1
DP2Tooltip Prostaglandin D2 receptor 2
EP (E2)Tooltip Prostaglandin E2 receptor
EP1Tooltip Prostaglandin EP1 receptor
EP2Tooltip Prostaglandin EP2 receptor
EP3Tooltip Prostaglandin EP3 receptor
EP4Tooltip Prostaglandin EP4 receptor
Unsorted
FP (F)Tooltip Prostaglandin F receptor
IP (I2)Tooltip Prostacyclin receptor
TP (TXA2)Tooltip Thromboxane receptor
Unsorted
Enzyme
(inhibitors)
COX
(
PTGS)
PGD2STooltip Prostaglandin D synthase
PGESTooltip Prostaglandin E synthase
PGFSTooltip Prostaglandin F synthase
PGI2STooltip Prostacyclin synthase
TXASTooltip Thromboxane A synthase
Others
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