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Selenium tetrachloride

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Selenium tetrachloride
Names
IUPAC name
Selenium tetrachloride
Other names
Selenium(IV) chloride, tetrachloro-λ4-selane
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.036 Edit 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 mass 220.771 g/mol
Appearance white to yellow crystals
Density 2.6 g/cm3, solid
Melting point sublimes 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: Toxic GHS08: Health hazard GHS09: 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 point non-flammable
Related compounds
Other anions
Selenium tetrafluoride
Selenium tetrabromide
Selenium dioxide
Other cations
Dichlorine monoxide
Sulfur tetrachloride
Tellurium tetrachloride
Related compounds
Selenium dichloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify  (what is checkYN ?)
Chemical compound

Selenium tetrachloride is the inorganic compound composed with the formula SeCl4. This compound exists as yellow to white volatile solid. It is one of two commonly available selenium chlorides, the other example being selenium monochloride, Se2Cl2. SeCl4 is used in the synthesis of other selenium compounds.

Synthesis and structure

[edit ]
Structure of selenium tetrachloride

The compound is prepared by treating selenium with chlorine.[3] When the reacting selenium is heated, the product sublimes from the reaction flask. The volatility of selenium tetrachloride can be exploited to purification of selenium.

Solid SeCl4 is actually a tetrameric cubane-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 teaching VSEPR rules of hypervalent molecules. As such, one would predict four bonds but five electron groups giving rise to a seesaw geometry. This clearly is not the case in the crystal structure. Others have suggested that the crystal structure can be represented as SeCl3+ and Cl. This formulation would predict a pyramidal 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 using triphenylstibine:

SeCl4 + SbPh3 → SeCl2 + Cl2SbPh3

Selenium tetrachloride reacts with water to give selenous and hydrochloric acids:[6] [page needed ]

SeCl4 + 3 H2O → H2SeO3 + 4 HCl

Upon treatment with selenium dioxide, it gives selenium 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 . Retrieved 2008年07月02日.
  2. ^ "323527 Selenium tetrachloride". Sigma-Aldrich. Retrieved 2008年07月02日.
  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. ^ a b Greenwood, 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.
Salts and covalent derivatives of the chloride ion
HCl He
FrCl RaCl2 ** LrCl3 RfCl4 DbCl5 SgO2Cl2 BhO3Cl Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
Receptor
(ligands)
DP (D2) Tooltip Prostaglandin D2 receptor
DP1 Tooltip Prostaglandin D2 receptor 1
DP2 Tooltip Prostaglandin D2 receptor 2
EP (E2) Tooltip Prostaglandin E2 receptor
EP1 Tooltip Prostaglandin EP1 receptor
EP2 Tooltip Prostaglandin EP2 receptor
EP3 Tooltip Prostaglandin EP3 receptor
EP4 Tooltip 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)
PGD2S Tooltip Prostaglandin D synthase
PGES Tooltip Prostaglandin E synthase
PGFS Tooltip Prostaglandin F synthase
PGI2S Tooltip Prostacyclin synthase
TXAS Tooltip Thromboxane A synthase
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