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1 Structure  





2 Synthesis and reactions  





3 References  














Trithiazyl trichloride






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From Wikipedia, the free encyclopedia
 


Trithiazyl trichloride
Names
Other names

thionitrosyl chloride

Identifiers

CAS Number

  • monomer: 17178-58-4
  • 3D model (JSmol)

  • monomer: Interactive image
  • ChemSpider
  • monomer: 123637
  • PubChem CID

  • monomer: 140196
  • CompTox Dashboard (EPA)

  • monomer: DTXSID70938043
    • InChI=1S/Cl3N3S3/c1-7-4-8(2)6-9(3)5-7

      Key: QBQMTUMJJWPFDJ-UHFFFAOYSA-N

    • monomer: InChI=1S/ClNS/c1-3-2

      Key: FWVIYFTZAHMHIO-UHFFFAOYSA-N

    • trimer: ClS1=NS(Cl)=NS(Cl)=N1

    • monomer: N#SCl

    Properties

    Chemical formula

    (NSCl)3
    Molar mass 244.55 g·mol−1
    Appearance white solid
    Melting point 168 °C (334 °F; 441 K)

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

    Infobox references

    Trithiazyl trichloride is the inorganic compound with the formula (NSCl)3. A white solid, it is a precursor to other sulfur nitrides,[1] but has no commercial applications.

    Structure[edit]

    The molecule is a 6-membered ring of alternating nitrogen and sulfur atoms, where each sulfur atom is attached to one chlorine atom by a single bond. The molecule contains alternating single and double bonds in the S3N3 core. The molecule has C3v symmetry. The S3N3 core is slightly ruffled structure with S-N distances of 160.5 pm. The S-Cl distances are 208 pm, and the chlorine atoms are mutually cis. The S centers are tetravalent and pyramidal. In contrast to the NSCl connectivity, nitrosyl chloride has the connectivity ONCl.[2][3]

    Synthesis and reactions[edit]

    Trithiazyl trichloride is obtained by chlorination of tetrasulfur tetranitride:

    3 S4N4 + 6 Cl2 → 4 (NSCl)3

    At 100 °C in vacuum, thiazyl chloride trimer undergoes crackingtothiazyl chloride monomer, which is a green gas.

    (−N=S(−Cl)−)3 → 3 N≡S−Cl

    In N≡S−Cl, chlorine is bonded to sulfur, in contrast to nitrosyl chloride O=N–Cl, where chlorine is bonded to nitrogen. In contrast, with six fewer electrons, cyanuric chloride is a planar ring.

    Alkoxide or silver salts displace the chlorides:[4]

    (-NS(Cl)-)3 + 3 NaOR → (-NS(OR)-)3 + 3 NaCl
    (-NS(Cl)-)3 + 3 AgX → (-NS(X)-)3 + 3 AgCl

    Treating thiazyl chloride with sulfur in the presence of antimony pentachloride gives dithionitronium hexachloroantimonate:[5]

    SNCl + S + SbCl5 → [NS2]SbCl6

    It reacts with nitrilestodithiadiazolium chlorides:[2]

    6 RCN + 4 (NSCl)3 → 6 [RCN2S2]+Cl + 3 Cl2 + 3 N2

    The compound oxidizes to the S(VI) compound (NSOCl)3, which exists as isomers.

    References[edit]

    1. ^ Jolly, William L.; Maguire, Keith D. (1967). Sulfur Nitrogen Chlorides. Inorganic Syntheses. Vol. IX. p. 102. doi:10.1002/9780470132401.ch27. ISBN 978-0-470-13240-1.
  • ^ a b Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  • ^ Wiegers, G. A.; Vos, A. (1966). "The Crystal Structures of Two Sulfur-Nitrogen Compounds with (S-N)3 Rings. II. Trithiazylchloride, (NSCl)3, at -130 C". Acta Crystallographica. 20 (2): 192. doi:10.1107/s0365110x66000410.
  • ^ Rawson, Jeremy M.; Banister, Arthur J.; Lavender, Ian (1995). "The Chemistry of Dithiadiazolylium and Dithiadiazolyl Rings". Adv. Heterocyc. Chem. 62: 146–147. doi:10.1016/S0065-2725(08)60422-5.
  • ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Trithiazyl_trichloride&oldid=1221885002"

    Categories: 
    Inorganic chlorine compounds
    Sulfur(IV) compounds
    Nitrides
    Sulfurnitrogen compounds
    Six-membered rings
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    This page was last edited on 2 May 2024, at 15:34 (UTC).

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