1,4,7-Trithiacyclononane
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1,4,7-Trithiacyclononane | |
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IUPAC name | 1,4,7-Trithionane |
Other names | 1,4,7-Trithiacyclononane, Triethylene trisulfide, 9-ane-S3, [9]aneS3 |
Identifiers | |
CAS number | [6573-11-1] |
PubChem | |
ChEBI | |
SMILES | C1CSCCSCCS1 |
Properties | |
Molecular formula | C6H12S3 |
Molar mass | 180.35 g/mol |
Appearance | Colourless solid |
Melting point |
78 - 81 °C |
Boiling point |
Decomp. |
Solubility in water | Insoluble |
Solubility | Chlorocarbons, acetone |
Hazards | |
Main hazards | Toxic (T) |
R-phrases | R36/37/38 |
S-phrases | S26, S36 |
Related compounds | |
Related compounds | Thiirane, 1,3,5-Trithiane, Triazacylononane |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and 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.
It 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]
[edit] References
- ^ Kueppers, H. J.; Wieghardt, K.; Nuber, B.; Weiss, J. W.; Bill, E. and Trautwein, A. X. (1987). "Crown Thioether Chemistry of Iron(II/III). Synthesis and Characterization of Low-spin Bis(1,4,7-trithiacyclononane)iron(III) and crystal structure of [FeII([9]aneS3)([9]aneS3(O))](ClO4)2.2NaClO4.H2O". Inorganic Chemistry 26: 3762–3769(8).
- ^ Gerber, D.; Chongsawangvirod, P.; Leung, A. K.; Ochrymowycz, L. A. (1977). "Synthesis of the Torsionally Strained Monocyclic Polythiaether 1,4,7-Trithiacyclononane". Journal of Organic Chemistry 42: 2644–2645(2).
- ^ Sellmann, D.; Zapf, L. (1984). "Simple Route to 1,4,7-Trithiacyclononane". Angewandte Chemie 96: 799–800(2).