Thiepine

In organic chemistry, thiepine (or thiepin) is an unsaturated seven-membered heterocyclic compound, with six carbon atoms and one sulfur atom. The parent compound, C6H6S is unstable and is predicted to be antiaromatic. Bulky derivatives have been isolated and shown by X-ray crystallography to have nonplanar C6S ring.[1]

Not to be confused with Thiepane.
Thiepine
Structural formula of thiepine
Ball-and-stick model of the thiepine molecule
Names
Preferred IUPAC name
Thiepine
Other names
Thiatropilidene
Thiepin
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C6H6S/c1-2-4-6-7-5-3-1/h1-6H checkY
    Key: BISQTCXKVNCDDA-UHFFFAOYSA-N checkY
  • S1C=CC=CC=C1
Properties
C6H6S
Molar mass 110.17 g·mol−1
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

Theoretical studies suggest that thiepine would eliminate a sulfur atom to form benzene. The intermediate is this process is the bicycle thianorcaradiene. In the complex with (η4-C6H6S)Fe(CO)3, the ring is stable.[2]

Benzothiepines have one fused benzene group and dibenzothiepines such as dosulepin and zotepine have two fused benzene groups. Damotepine is another thiepin derivative.

The chemical structure of the dibenzothiepine zotepine.

See also

References
  1. Schwan, A. L., "Thiepins" Science of Synthesis, 2004, volume 17, 705. doi:10.1055/sos-SD-017-01065
  2. Nishino, K.; Takagi, M.; Kawata, T.; Murata, I.; Inanaga, J.; Nakasuji, K., "Thiepine-iron tricarbonyl: stabilization of thermally labile parent thiepine by transition metal complexation", J. Am. Chem. Soc. 1991, volume 113, 5059-5060.


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