1,4,7-Trithiacyclononane

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1,4,7-Trithiacyclononane
Structure of 1,4,7-Trithiacyclononane.png
1,4,7-Trithiacyclononane molecule
Names
IUPAC name
1,4,7-Trithionane
Other names
1,4,7-Trithiacyclononane, Triethylene trisulfide, 9-ane-S3, [9]aneS3
Identifiers
6573-11-1 N
ChEBI CHEBI:37418 YesY
ChemSpider 331656 YesY
Jmol 3D model Interactive image
Interactive image
PubChem 373835
  • InChI=1S/C6H12S3/c1-2-8-5-6-9-4-3-7-1/h1-6H2 YesY
    Key: PQNPKQVPJAHPSB-UHFFFAOYSA-N YesY
  • InChI=1/C6H12S3/c1-2-8-5-6-9-4-3-7-1/h1-6H2
    Key: PQNPKQVPJAHPSB-UHFFFAOYAS
  • C1CSCCSCCS1
  • S1CCSCCSCC1
Properties
C6H12S3
Molar mass 180.35 g/mol
Appearance Colourless solid
Melting point 78 to 81 °C (172 to 178 °F; 351 to 354 K)
Boiling point decomposes
Insoluble
Solubility Chlorocarbons, acetone
Vapor pressure {{{value}}}
Related compounds
Related compounds
Thiirane, 1,3,5-Trithiane, Triazacylononane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

1,4,7-Trithiacyclononane, also called 9-ane-S3, is the heterocyclic compound with the formula (CH2CH2S)3. This cyclic thioether is most often encountered as a tridentate ligand in coordination chemistry.

9-ane-S3 forms complexes with many metal ions, including those considered hard, such as copper(II) and iron(II).[1] Most of its complexes have the formula [M(9-ane-S3)2]2+ and are octahedral. The point group of [M(9-ane-S3)2]2+ is S6.

Synthesis

This compound was first reported in 1977,[2] and the current synthesis entails the assembly within the coordination sphere of a metal ion followed by decomplexation:[3]

Synthesis of 9S3.png

References

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