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1 Structure and properties  





2 Preparation  





3 Reactions  





4 References  














Selenium monochloride






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From Wikipedia, the free encyclopedia
 

(Redirected from Diselenium dichloride)

Diselenium dichloride
Names
IUPAC name

Diselenium dichloride

Other names
  • 1,2-Dichlorodiselane
  • Dichlorodiselane
  • Dichlorodiselenide
  • Selenium chloride
  • Selenium monochloride
  • Identifiers

    CAS Number

    3D model (JSmol)

    ChemSpider
    ECHA InfoCard 100.030.022 Edit this at Wikidata
    EC Number
    • 233-037-8

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/Cl2Se2/c1-3-4-2 ☒N

      Key: VIEXQFHKRAHTQS-UHFFFAOYSA-N ☒N

    • InChI=1/Cl2Se2/c1-3-4-2

      Key: VIEXQFHKRAHTQS-UHFFFAOYAC

    • Cl[Se][Se]Cl

    Properties

    Chemical formula

    Se2Cl2
    Molar mass 228.84 g·mol−1
    Appearance Reddish-brown oily liquid
    Density 2.7741 g/cm3
    Melting point −85 °C (−121 °F; 188 K)
    Boiling point 127 °C (261 °F; 400 K) at 0.997 atm

    Solubility in water

    insoluble
    Solubility in other solvents Soluble in chloroform, carbon disulfide, and acetonitrile

    Magnetic susceptibility (χ)

    −94.8·10−6cm3/mol
    Hazards
    GHS labelling:

    Pictograms

    GHS05: CorrosiveGHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard

    Signal word

    Danger

    Hazard statements

    H301, H311, H314, H331, H373, H410

    Precautionary statements

    P260, P261, P264, P270, P271, P273, P280, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P311, P312, P314, P321, P322, P330, P361, P363, P391, P403+P233, P405, P501

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Selenium monochlorideordiselenium dichloride is an inorganic compound with the formula Se2Cl2. Although a common name for the compound is selenium monochloride, reflecting its empirical formula, IUPAC does not recommend that name, instead preferring the more descriptive diselenium dichloride.

    Diselenium dichloride is a reddish-brown, oily liquid that hydrolyses slowly. It exists in chemical equilibrium with SeCl2, SeCl4, chlorine, and elemental selenium.[1] Diselenium dichloride is mainly used as a reagent for the synthesis of Se-containing compounds.

    Structure and properties

    [edit]

    Dielenium dichloride has the connectivity Cl−Se−Se−Cl. With a nonplanar structure, it has C2 molecular symmetry, similar to hydrogen peroxide and disulfur dichloride, which is referred to as gauche. The Se-Se bond length is 223 pm, and the Se-Cl bond lengths are 220 pm. The dihedral angle between the Cla−Se−Se and Se−Se−Clb planes is 87°.[2]

    Preparation

    [edit]

    Early routes to diselenium dichloride involved chlorination of elemental selenium.[3] An improved method involves the reaction of a mixture of selenium, selenium dioxide, and hydrochloric acid:[4]

    3 Se + SeO2 + 4 HCl → 2 Se2Cl2 + 2 H2O

    A dense layer of diselenium dichloride settles from the reaction mixture, which can be purified by dissolving it in fuming sulfuric acid and reprecipitating it with hydrochloric acid. A second method for the synthesis involves the reaction of selenium with oleum and hydrochloric acid:[4]

    2 Se + 2 SO3 + 3 HCl → Se2Cl2 + SO2 + H2O + SO2(OH)Cl

    The crude diselenium dichloride is removed via separatory funnel. Diselenium dichloride cannot be distilled without decomposition, even at reduced pressure.[4]

    Inacetonitrile solutions, it exists in equilibrium with SeCl2 and SeCl4.[5] Selenium dichloride degrades to diselenium dichloride after a few minutes at room temperature:[6]

    3 SeCl2 → Se2Cl2 + SeCl4

    Reactions

    [edit]

    Diselenium dichloride is an electrophilic selenizing agent, and thus it reacts with simple alkenes to give bis(β-chloroalkyl)selenide and bis(chloroalkyl)selenium dichloride. It converts hydrazones of hindered ketones into the corresponding selenoketones, the structural analogs of ketones whereby the oxygen atom is replaced with a selenium atom.[7] Finally, the compound has been used to introduce bridging selenium ligands between the metal atoms of some iron and chromium carbonyl complexes.[7]

    References

    [edit]
    1. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  • ^ Kniep, Rüdiger; Körte, Lutz; Mootz, Dietrich (1 January 1983). "Kristallstrukturen von Verbindungen A2X2 (A = S, Se; X = Cl, Br)". Zeitschrift für Naturforschung B. 38 (1): 1–6. doi:10.1515/znb-1983-0102.
  • ^ Lenher, Victor; Kao, C. H. (1925). "The Preparation of Selenium Monochloride and Monobromide". Journal of the American Chemical Society. 47 (3): 772–774. doi:10.1021/ja01680a025.
  • ^ a b c Fehér, F. (1963). "Diselenium Dichloride". In Brauer, G. (ed.). Handbook of Preparative Inorganic Chemistry. Vol. 1 (2nd ed.). New York: Academic Press. pp. 422–423.
  • ^ Lamoureux, Marc; Milne, John (1990). "Selenium chloride and bromide equilibria in aprotic solvents; a Se77 NMR study". Polyhedron. 9 (4): 589–595. doi:10.1016/S0277-5387(00)86238-5.
  • ^ Maaninen, Arto; Chivers, Tristram; Parvez, Masood; Pietikäinen, Jarkko; Laitinen, Risto S. (1999). "Syntheses of THF Solutions of SeX2(X = Cl, Br) and a New Route to Selenium Sulfides SenS8−n(n = 1−5): X-ray Crystal Structures of SeCl2(tht)2 and SeCl2·tmtu". Inorganic Chemistry. 38 (18): 4093–4097. doi:10.1021/ic981430h.
  • ^ a b Back, Thomas G.; Moussa, Ziad (2003). "Diselenium Dichloride". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rn00201. ISBN 0-471-93623-5.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Selenium_monochloride&oldid=1215852603"

    Categories: 
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    Nonmetal halides
    Chalcohalides
    Selenium halides
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    This page was last edited on 27 March 2024, at 14:26 (UTC).

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